100 results on '"Lechner JF"'
Search Results
2. Gingers and Their Purified Components as Cancer Chemopreventative Agents.
- Author
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Lechner JF and Stoner GD
- Subjects
- Animals, Chemoprevention, Humans, Structure-Activity Relationship, Anticarcinogenic Agents chemistry, Anticarcinogenic Agents pharmacology, Zingiber officinale chemistry, Plant Extracts chemistry, Plant Extracts pharmacology
- Abstract
Chemoprevention by ingested substituents is the process through which nutraceuticals and/or their bioactive components antagonize carcinogenesis. Carcinogenesis is the course of action whereby a normal cell is transformed into a neoplastic cell. This latter action involves several steps, starting with initiation and followed by promotion and progression. Driving these stages is continued oxidative stress and inflammation, which in turn, causes a myriad of aberrant gene expressions and mutations within the transforming cell population and abnormal gene expressions by the cells within the surrounding lesion. Chemoprevention of cancer with bioreactive foods or their extracted/purified components occurs primarily via normalizing these inappropriate gene activities. Various foods/agents have been shown to affect different gene expressions. In this review, we discuss how the chemoprevention activities of gingers antagonize cancer development.
- Published
- 2019
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3. Red Beetroot and Betalains as Cancer Chemopreventative Agents.
- Author
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Lechner JF and Stoner GD
- Subjects
- Animals, Anticarcinogenic Agents chemistry, Anticarcinogenic Agents isolation & purification, Antioxidants chemistry, Antioxidants isolation & purification, Betalains chemistry, Betalains isolation & purification, Carcinogenesis genetics, Carcinogenesis metabolism, Carcinogenesis pathology, Cell Line, Tumor, Flavonols chemistry, Flavonols isolation & purification, Flavonols pharmacology, Humans, Mice, Neoplasm Proteins antagonists & inhibitors, Neoplasm Proteins genetics, Neoplasm Proteins metabolism, Neoplasms genetics, Neoplasms metabolism, Neoplasms pathology, Phenols chemistry, Phenols isolation & purification, Phenols pharmacology, Plant Extracts chemistry, Plant Roots chemistry, Triterpenes chemistry, Triterpenes isolation & purification, Triterpenes pharmacology, Xenograft Model Antitumor Assays, Anticarcinogenic Agents pharmacology, Antioxidants pharmacology, Beta vulgaris chemistry, Betalains pharmacology, Carcinogenesis drug effects, Gene Expression Regulation, Neoplastic drug effects, Neoplasms prevention & control
- Abstract
Carcinogenesis is the process whereby a normal cell is transformed into a neoplastic cell. This action involves several steps starting with initiation and followed by promotion and progression. Driving these stages are oxidative stress and inflammation, which in turn encompasses a myriad of aberrant gene expressions, both within the transforming cell population and the cells within the surrounding lesion. Chemoprevention of cancer with bioreactive foods or their extracted/purified components occurs via normalizing these inappropriate gene activities. Various foods/agents have been shown to affect different gene expressions. In this review, we discuss whereby the chemoprevention activities of the red beetroot itself may disrupt carcinogenesis and the activities of the water-soluble betalains extracted from the plant.
- Published
- 2019
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4. Black raspberries suppress colonic adenoma development in ApcMin/+ mice: relation to metabolite profiles.
- Author
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Pan P, Skaer CW, Wang HT, Stirdivant SM, Young MR, Oshima K, Stoner GD, Lechner JF, Huang YW, and Wang LS
- Subjects
- Adenoma metabolism, Adenoma pathology, Animals, Colorectal Neoplasms metabolism, Colorectal Neoplasms pathology, Disease Models, Animal, Gene Expression Regulation, Neoplastic drug effects, Humans, Intestinal Mucosa drug effects, Mice, Mice, Transgenic, Putrescine biosynthesis, alpha-Linolenic Acid biosynthesis, Adenoma diet therapy, Adenomatous Polyposis Coli Protein genetics, Colorectal Neoplasms diet therapy, Fruit, Rubus
- Abstract
Freeze-dried black raspberries (BRBs) have demonstrated chemopreventive effects in a dietary intervention trial with human colorectal cancer patients. The aim of this study was to investigate BRB-caused metabolite changes using the Apc(Min/+) mouse as a model of human colorectal cancer. Wild-type (WT) mice were fed control diet, and Apc(Min/+) mice were fed either control diet or control diet supplemented with 5% BRBs for 8 weeks. Colonic and intestinal polyp size and number were measured. A non-targeted metabolomic analysis was conducted on colonic mucosa, liver and fecal specimens. Eight weeks of BRB treatment significantly decreased intestinal and colonic polyp number and size in Apc(Min/+) mice. The apc gene mutation significantly changed 52 metabolites in colonic mucosa associated with increased amino acid and decreased lipid metabolites, as well as 39 liver and 8 fecal metabolites. BRBs significantly reversed 23 apc-regulated metabolites, including 13 colonic mucosa, 8 liver and 2 fecal metabolites that were involved in amino acid, glutathione, lipid and nucleotide metabolism. Of these, changes in eight metabolites were linearly correlated with decreased colonic polyp number and size in BRB-treated Apc(Min/+) mice. Elevated levels of putrescine and linolenate in Apc(Min/+) mice were significantly decreased by BRBs. Ornithine decarboxylase expression, the key enzyme in putrescine generation, was fully suppressed by BRBs. These results suggest that BRBs produced beneficial effects against colonic adenoma development in Apc(Min/+) mice and modulated multiple metabolic pathways. The metabolite changes produced by BRBs might potentially reflect the BRB-mediated chemopreventive effects in colorectal cancer patients., (© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2015
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5. Beneficial Regulation of Metabolic Profiles by Black Raspberries in Human Colorectal Cancer Patients.
- Author
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Pan P, Skaer CW, Stirdivant SM, Young MR, Stoner GD, Lechner JF, Huang YW, and Wang LS
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- Administration, Oral, Chromatography, Liquid, Colorectal Neoplasms diet therapy, Humans, Tandem Mass Spectrometry, Colorectal Neoplasms blood, Colorectal Neoplasms urine, Fruit chemistry, Metabolome drug effects, Rubus chemistry
- Abstract
Dietary intervention of freeze-dried black raspberries (BRBs) in a group of human colorectal cancer patients has demonstrated beneficial effects, including proapoptosis, antiproliferation, and antiangiogenesis. The aim of this study was to investigate BRB-mediated metabolite changes from this same cohort of patients. Twenty-eight colorectal cancer patients were given 60 g BRB powder daily for 1 to 9 weeks. Urine and plasma specimens were collected before and after BRB intervention. A mass spectrometry-based nontargeted metabolomic analysis was conducted on each specimen. A total of more than 400 metabolites were annotated in each specimen. Of these 34 and 6 metabolites were significantly changed by BRBs in urine and plasma, respectively. Increased levels of 4-methylcatechol sulfate in both post-BRB urine and post-BRB plasma were significantly correlated with a higher level of apoptotic marker (TUNEL) in post-BRB tumors. One tricarboxylic acid (TCA) cycle metabolites, cis-aconitate, was increased in post-BRB urine. Furthermore, BRB-derived polyphenols were absorbed and metabolized to various benzoate species, which were significantly increased in post-BRB specimens. Increased benzoate levels were positively correlated with enhanced levels of amino acid metabolite. These results suggest that BRBs induce significant metabolic changes and affect energy generating pathways.This study supports the hypothesis that BRBs might be beneficial to colorectal cancer patients through the regulation of multiple metabolites., (©2015 American Association for Cancer Research.)
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- 2015
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6. Black raspberries protectively regulate methylation of Wnt pathway genes in precancerous colon tissue.
- Author
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Wang LS, Kuo CT, Huang TH, Yearsley M, Oshima K, Stoner GD, Yu J, Lechner JF, and Huang YW
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- Animals, Colitis, Ulcerative genetics, Colitis, Ulcerative metabolism, Colon metabolism, Colon pathology, DNA (Cytosine-5-)-Methyltransferases genetics, DNA (Cytosine-5-)-Methyltransferases metabolism, DNA-Binding Proteins genetics, DNA-Binding Proteins metabolism, Diet, Female, Histone Deacetylase 1 genetics, Histone Deacetylase 1 metabolism, Histone Deacetylase 2 genetics, Histone Deacetylase 2 metabolism, Humans, Immunoenzyme Techniques, Mice, Mice, Knockout, Precancerous Conditions genetics, Precancerous Conditions metabolism, Promoter Regions, Genetic genetics, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, DNA, DNA Methyltransferase 3B, Colitis, Ulcerative prevention & control, DNA Methylation, Fruit chemistry, Interleukin-10 physiology, Precancerous Conditions prevention & control, Rosaceae chemistry, Wnt Signaling Pathway genetics
- Abstract
Ulcerative colitis is frequently an intermediate step to colon cancer. The interleukin-10 knockout mouse is a genetic model of this progression. We report that knockout mice fed 5% black raspberries (BRB) had significantly less colonic ulceration as compared with knockout mice that consumed the control diet. Dysfunction of the Wnt signaling pathway is a key event in ulcerative colitis-associated colon carcinogenesis. Therefore, we investigated the effects of BRBs on the Wnt pathway and found that the BRB-fed knockout mice exhibited a significantly lower level of β-catenin nuclear translocation. We followed-up this observation by evaluating the effect of BRBs on selected Wnt pathway antagonists. The mRNA expression levels of wif1, sox17, and qki were diminished in the knockout mice, whereas they were expressed at normal levels in knockout mice that were fed BRBs. The lower mRNA expression of these genes in the colon from the knockout mice correlated with hypermethylation of their promoter regions; BRBs decreased their promoter methylation and increased mRNA expression of these genes. This hypomethylation was associated with elevated protein expression of key proteins/enzymes that augment methylation, for example, dnmt3b, hdac1, hdac2, and mbd2 in the knockout mice; in addition, BRBs decreased the protein expression of these proteins/enzymes. The knockout mouse model recapitulates what occurs in human ulcerative colitis. Promoter methylation of CDH1 and SFRP1 was significantly higher in human ulcerative colitis tissues compared with their adjacent normal tissues. In conclusion, our results suggest that BRBs inhibit colonic ulceration and, ultimately, colon cancer partly through inhibiting aberrant epigenetic events that dysregulate Wnt signaling.
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- 2013
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7. Gene-Diet Interactions on Colorectal Cancer Risk.
- Author
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Wang LS, Kuo CT, Huang YW, Stoner GD, and Lechner JF
- Abstract
There has been increasing interest lately in understanding how natural dietary antioxidants affect chemoprevention, and recently, there has been a merging of information about antioxidants, endogenous and exogenous reactive oxygen and nitrogen species (RONS), and inflammation. RONS normally serve the cells as second messengers to regulate many of the intracellular signaling cascades that govern multiple cellular activities. However, when the amount of RONS exceeds the cell's ability to metabolize/eliminate them, the cell becomes stressed and acquires genetic and epigenetic aberrations and dysregulated intracellular signaling cascades. In addition, there has been a better understanding of the role of tissue inflammation in the carcinogenesis process. Herein we integrate these fields to explain where RONS arise and how natural dietary antioxidants are principally working through refurbishing pathways that use RONS as second messengers.
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- 2012
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8. Drinking water with red beetroot food color antagonizes esophageal carcinogenesis in N-nitrosomethylbenzylamine-treated rats.
- Author
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Lechner JF, Wang LS, Rocha CM, Larue B, Henry C, McIntyre CM, Riedl KM, Schwartz SJ, and Stoner GD
- Subjects
- Animals, Antigens, CD34 immunology, Apoptosis drug effects, Cell Proliferation drug effects, Dimethylnitrosamine adverse effects, Disease Models, Animal, Esophageal Neoplasms chemically induced, Esophageal Neoplasms immunology, Esophageal Neoplasms pathology, Food Coloring Agents analysis, Humans, Leukocyte Common Antigens immunology, Male, Plant Extracts analysis, Plant Roots chemistry, Random Allocation, Rats, Rats, Sprague-Dawley, Water analysis, Beta vulgaris chemistry, Dimethylnitrosamine analogs & derivatives, Esophageal Neoplasms physiopathology, Food Coloring Agents administration & dosage, Plant Extracts administration & dosage, Water administration & dosage
- Abstract
This study was undertaken to determine if the oral consumption of red beetroot food color would result in an inhibition of N-nitrosomethylbenzylamine (NMBA)-induced tumors in the rat esophagus. Rats were treated with NMBA and given either regular water ad libitum or water containing 78 microg/mL commercial red beetroot dye, E162. The number of NMBA-induced esophageal papillomas was reduced by 45% (P < .001) in animals that received the food color compared to controls. The treatment also resulted in reduced rates of cell proliferation in both precancerous esophageal lesions and in papillomas of NMBA-treated rats, as measured by immunohistochemical staining of Ki-67 in esophageal tissue specimens. The effects of beetroot food color on angiogenesis (microvessel density by CD34 immunostaining), inflammation (by CD45 immunostaining), and apoptosis (by terminal deoxynucleotidyl transferase dUTP nick end-labeling staining) in esophageal tissue specimens were also determined. Compared to rats treated with NMBA only, the levels of angiogenesis and inflammation in the beetroot color-consuming animals were reduced, and the apoptotic rate was increased. Thus, the mechanism(s) of chemoprevention by the active constituents of red beetroot color include reducing cell proliferation, angiogenesis, and inflammation and stimulating apoptosis. Importantly, consumption of the dye in the drinking water for a period of 35 weeks did not appear to induce any overt toxicity. Based on the fact that red beetroot color contains betanins, which have strong antioxidant activity, it is postulated that these effects are mediated through inhibition of oxygen radical-induced signal transduction. However, the sum of constituents of E162 has not been determined, and other components with other mechanisms may also be involved in antagonizing cancer development.
- Published
- 2010
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9. Anthocyanins in black raspberries prevent esophageal tumors in rats.
- Author
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Wang LS, Hecht SS, Carmella SG, Yu N, Larue B, Henry C, McIntyre C, Rocha C, Lechner JF, and Stoner GD
- Subjects
- Animals, Apoptosis drug effects, Blotting, Western, Cell Proliferation drug effects, Freeze Drying, Image Processing, Computer-Assisted, Immunohistochemistry, Inflammation drug therapy, Male, Neovascularization, Pathologic drug therapy, Rats, Rats, Inbred F344, Anthocyanins pharmacology, Esophageal Neoplasms prevention & control, Fruit chemistry, Phytotherapy, Plant Extracts pharmacology, Rosaceae chemistry
- Abstract
Diets containing freeze-dried black raspberries (BRB) suppress the development of N-nitrosomethylbenzylamine (NMBA)-induced tumors in the rat esophagus. Using bioassay-directed fractionation, the anthocyanins in BRB were found to be the most active constituents for down-regulation of carcinogen-induced nuclear factor-kappaB and activator protein-1 expression in mouse epidermal cells in vitro. The present study was undertaken, therefore, to determine if the anthocyanins contribute to the chemopreventive activity of BRB in vivo. F344 rats consumed diets containing either (a) 5% whole BRB powder, (b) an anthocyanin-rich fraction, (c) an organic solvent-soluble extract (a-c each contained approximately 3.8 micromol anthocyanins/g diet), (d) an organic-insoluble (residue) fraction (containing 0.02 mumol anthocyanins/g diet), (e) a hexane extract, and (f) a sugar fraction (e and f had only trace quantities of anthocyanins), all derived from BRB. Animals were fed diets 2 weeks before treatment with NMBA and throughout the bioassay. Control rats were treated with NMBA only. Animals were killed at week 30, and esophageal tumors were enumerated. The anthocyanin treatments (diet groups a-c) were about equally effective in reducing NMBA tumorigenesis in the esophagus, indicating that the anthocyanins in BRB have chemopreventive potential. The organic-insoluble (residue) fraction (d) was also effective, suggesting that components other than berry anthocyanins may be chemopreventive. The hexane and sugar diets were inactive. Diet groups a, b, and d all inhibited cell proliferation, inflammation, and angiogenesis and induced apoptosis in both preneoplastic and papillomatous esophageal tissues, suggesting similar mechanisms of action by the different berry components.
- Published
- 2009
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10. Carcinogen-altered genes in rat esophagus positively modulated to normal levels of expression by both black raspberries and phenylethyl isothiocyanate.
- Author
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Stoner GD, Dombkowski AA, Reen RK, Cukovic D, Salagrama S, Wang LS, and Lechner JF
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- Animals, Apoptosis drug effects, Apoptosis genetics, Diet, Dimethylnitrosamine toxicity, Esophagus metabolism, Esophagus pathology, Male, Neovascularization, Pathologic genetics, Rats, Rats, Inbred F344, Signal Transduction genetics, Carcinogens toxicity, Dimethylnitrosamine analogs & derivatives, Esophagus drug effects, Fruit, Gene Expression Regulation drug effects, Isothiocyanates pharmacology
- Abstract
Our recent study identified 2,261 dysregulated genes in the esophagi of rats that received a 1-week exposure to the carcinogen N-nitrosomethylbenzylamine (NMBA). We further reported that 1,323 of these genes were positively modulated to near-normal levels of expression in NMBA-treated animals that consumed dietary phenylethyl isothiocyanate (PEITC), a constituent of cruciferous vegetables. Herein, we report our results with companion animals that were fed a diet containing 5% freeze-dried black raspberries (BRB) instead of PEITC. We found that 462 of the 2,261 NMBA-dysregulated genes in rat esophagus were restored to near-normal levels of expression by BRB. Further, we have identified 53 NMBA-dysregulated genes that are positively modulated by both PEITC and BRB. These 53 common genes include genes involved in phase I and II metabolism, oxidative damage, and oncogenes and tumor suppressor genes that regulate apoptosis, cell cycling, and angiogenesis. Because both PEITC and BRB maintain near-normal levels of expression of these 53 genes, their dysregulation during the early phase of NMBA-induced esophageal cancer may be especially important in the genesis of the disease.
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- 2008
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11. Effects of a black raspberry diet on gene expression in the rat esophagus.
- Author
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Lechner JF, Reen RK, Dombkowski AA, Cukovic D, Salagrama S, Wang LS, and Stoner GD
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- Animals, Diet, Esophagus metabolism, Esophagus pathology, Male, Oligonucleotide Array Sequence Analysis, Rats, Rats, Inbred F344, Transcription, Genetic drug effects, Esophagus drug effects, Gene Expression Regulation drug effects, Rosaceae
- Abstract
A diet containing 5% freeze-dried black raspberries (BRB) markedly inhibits esophageal cancer in rats treated with the carcinogen, N-Nitrosomethylbenzylamine (NMBA). We previously identified esophageal genes that become dysregulated after short-term treatment of rats with NMBA and determined which genes are maintained at near-normal levels of expression if the animals were fed 5% BRB prior to and during NMBA treatment. In this study, we report the effects of the BRB diet on gene expression in esophagi from untreated (control) animals. After 3 wk on a 5% BRB diet, control esophagi were excised, stripped of the submucosal and muscularis layers, and processed for histology and microarray profiling. RNA microarrays revealed that the BRB altered the expression levels of 36 genes; 24 were upregulated, and 12 were downregulated. Among the upregulated genes are genes associated with cellular matrix, signaling cascades, transcription regulation, apoptosis, metabolism, and intriguingly, contraction. Most of the downregulated transcripts are involved in cell regulation, signal transduction, and metabolism. Histopathological analyses revealed that the BRB have little or no effect on esophageal morphology. In conclusion, histological and molecular studies indicate that a 5% BRB diet produces only modest effects on the esophagus, the target tissue for NMBA carcinogenesis in the rat.
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- 2008
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12. Cancer prevention with freeze-dried berries and berry components.
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Stoner GD, Wang LS, Zikri N, Chen T, Hecht SS, Huang C, Sardo C, and Lechner JF
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- Animals, Chemoprevention, Freeze Drying, Humans, Powders, Rats, Colonic Neoplasms prevention & control, Esophageal Neoplasms prevention & control, Fruit chemistry
- Abstract
Our laboratory is developing a food-based approach to the prevention of esophageal and colon cancer utilizing freeze-dried berries and berry extracts. Dietary freeze-dried berries were shown to inhibit chemically induced cancer of the rodent esophagus by 30-60% and of the colon by up to 80%. The berries are effective at both the initiation and promotion/progression stages of tumor development. Berries inhibit tumor initiation events by influencing carcinogen metabolism, resulting in reduced levels of carcinogen-induced DNA damage. They inhibit promotion/progression events by reducing the growth rate of pre-malignant cells, promoting apoptosis, reducing parameters of tissue inflammation and inhibiting angiogenesis. On a molecular level, berries modulate the expression of genes involved with proliferation, apoptosis, inflammation and angiogenesis. We have recently initiated clinical trials; results from a toxicity study indicated that freeze-dried black raspberries are well tolerated in humans when administered orally for 7 days at a dose of 45 g per day. Several Phase IIa clinical trials are underway in patients at high risk for esophagus and colon cancer; i.e., Barrett's esophagus, esophageal dysplasia and colonic polyps, to determine if berries will modulate various histological and molecular biomarkers of development of these diseases.
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- 2007
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13. Human lung cancer cells and tissues partially recapitulate the homeobox gene expression profile of embryonic lung.
- Author
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Lechner JF, Wang Y, Siddiq F, Fugaro JM, Wali A, Lonardo F, Willey JC, Harris CC, and Pass HI
- Subjects
- DNA Primers, Humans, Lung Neoplasms physiopathology, Tumor Cells, Cultured, Gene Expression Regulation, Developmental, Gene Expression Regulation, Neoplastic, Genes, Homeobox, Lung embryology, Lung Neoplasms genetics
- Abstract
The fetal cell features of tumor cells suggest that neoplasia arises through a process of defective ontogeny. Homeobox (HOX) genes code for transcription factors that orchestrate organogenesis patterning and maintain tissue homeostasis. Thus, if detective ontogeny is a mechanism in cancer development, it can be hypothesized that tumor cells should express the HOX genes normally expressed by the embryonic cells of that tissue. Our data herein indicate that some HOX genes, whose expression is normally restricted to pulmonary embryogenesis, are re-expressed in lung cancer cells. However, lung cancer cells also frequently and inappropriately express HOX genes that are not normally expressed in lung tissue, regardless of developmental stage. Thus, whereas re-expression of some of the embryo-specific HOX genes is a common feature of lung cancer, tumors do not faithfully recapitulate the expression pattern of cells that participate in the early stages of lung development.
- Published
- 2002
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14. Aberrant promoter methylation in bronchial epithelium and sputum from current and former smokers.
- Author
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Belinsky SA, Palmisano WA, Gilliland FD, Crooks LA, Divine KK, Winters SA, Grimes MJ, Harms HJ, Tellez CS, Smith TM, Moots PP, Lechner JF, Stidley CA, and Crowell RE
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- Adult, Aged, Aged, 80 and over, Apoptosis Regulatory Proteins, Bronchi metabolism, Bronchi ultrastructure, Calcium-Calmodulin-Dependent Protein Kinases genetics, Case-Control Studies, Cells, Cultured, Chromosomes, Human, Pair 9, Death-Associated Protein Kinases, Epithelial Cells metabolism, Epithelial Cells physiology, Epithelial Cells ultrastructure, Female, Genes, p16 physiology, Humans, Loss of Heterozygosity, Lung Neoplasms etiology, Lung Neoplasms metabolism, Male, Middle Aged, Neoplasm Proteins genetics, O(6)-Methylguanine-DNA Methyltransferase genetics, Smoking adverse effects, Smoking metabolism, Sputum cytology, Bronchi physiology, DNA Methylation, Genes, Tumor Suppressor, Lung Neoplasms genetics, Promoter Regions, Genetic, Smoking genetics, Sputum metabolism, Tumor Suppressor Proteins
- Abstract
Recent studies from our laboratory suggest that gene-specific methylation changes in sputum could be good intermediate markers for the early detection of lung cancer and defining the efficacy of chemopreventive interventions. The purpose of our study was to determine the prevalence for aberrant promoter methylation of the p16, O(6)-methylguanine-DNA methyltransferase (MGMT), death-associated protein (DAP) kinase, and Ras effector homologue (RASSFIA) genes in nonmalignant bronchial epithelial cells from current and former smokers in a hospital-based, case control study of lung cancer. The relationship between loss of heterozygosity, at 9p and p16 methylation in bronchial epithelium and the prevalence for methylation of these four genes in sputum from cancer-free, current and former smokers were also determined. Aberrant promoter methylation of p16 was seen in at least one bronchial epithelial site from 44% of cases and controls. Methylation of the DAP kinase gene was seen in only 1 site from 5 cases and 4 controls, whereas methylation of the RASSFIA was not detected in the bronchial epithelium. Promoter methylation for p16 and DAP kinase was seen as frequently in bronchial epithelium from current smokers as from former smokers. No promoter methylation of these genes was detected in bronchial epithelium from never-smokers. Methylation of the p16 gene was detected in sputum from 23 of 66 controls. DAP kinase gene promoter methylation was also seen in sputum from 16 controls, and 8 of these subjects were positive for p16 methylation. Methylation of the MGMT gene was seen in sputum from 9 controls, whereas RASSFIA promoter methylation was only seen in 2 controls. The correlation between p16 status in the bronchial epithelium obtained from lung lobes that did not contain the primary tumor and the tumor itself was examined. Seventeen of 18 tumors (94%) showed an absolute concordance, being either methylated in the tumor and at least 1 bronchial epithelial site, or unmethylated in both tumor and bronchial epithelium. These results indicate that aberrant promoter hypermethylation of the p16 gene, and to a lesser extent, DAP kinase, occurs frequently in the bronchial epithelium of lung cancer cases and cancer-free controls and persists after smoking cessation. The strong association seen between p16 methylation in the bronchial epithelium and corresponding primary tumor substantiates that inactivation of this gene, although not transforming by itself, is likely permissive for the acquisition of additional genetic and epigenetic changes leading to lung cancer.
- Published
- 2002
15. Reproducible gene expression measurement among multiple laboratories obtained in a blinded study using standardized RT (StaRT)-PCR.
- Author
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Crawford EL, Peters GJ, Noordhuis P, Rots MG, Vondracek M, Grafström RC, Lieuallen K, Lennon G, Zahorchak RJ, Georgeson MJ, Wali A, Lechner JF, Fan PS, Kahaleh MB, Khuder SA, Warner KA, Weaver DA, and Willey JC
- Subjects
- Binding, Competitive genetics, Cell Line, DNA, Complementary genetics, Databases, Genetic, Double-Blind Method, Gene Expression, Gene Expression Profiling classification, Gene Expression Profiling statistics & numerical data, Humans, Lung chemistry, Lung cytology, Lung metabolism, RNA, Messenger genetics, Reverse Transcriptase Polymerase Chain Reaction statistics & numerical data, Templates, Genetic, Terminology as Topic, Gene Expression Profiling standards, Reverse Transcriptase Polymerase Chain Reaction standards
- Abstract
Background: A method that provides standardized data and is relatively inexpensive and capable of high throughput is a prerequisite to the development of a meaningful gene expression database suitable for conducting multi-institutional clinical studies based on expression measurement. Standardized RT (StaRT)-PCR has all these characteristics. In addition, the method must be reproducible. StaRT-PCR has high intralaboratory reproducibility. The purpose of this study is to determine whether StaRT-PCR provides similar interlaboratory reproducibility., Methods and Results: In a blinded interlaboratory study, expression of ten genes was measured by StaRT-PCR in a complementary DNA sample provided to each of four laboratories. The average coefficient of variation for interlaboratory comparison of the nine quantifiable genes was 0.48. In all laboratories, expression of one of the genes was too low to be measured., Conclusion: Because StaRT-PCR data are standardized and numerical and the method is reproducible among multiple laboratories, it will allow development of a meaningful gene expression database.
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- 2001
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16. Human papillomavirus type 16 is an important infectious factor in the high incidence of esophageal cancer in Anyang area of China.
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Li T, Lu ZM, Chen KN, Guo M, Xing HP, Mei Q, Yang HH, Lechner JF, and Ke Y
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- China epidemiology, DNA, Viral genetics, Esophageal Neoplasms epidemiology, Esophageal Neoplasms pathology, Female, Humans, In Situ Hybridization, Incidence, Male, Middle Aged, Oncogene Proteins, Viral genetics, Papillomaviridae classification, Papillomavirus E7 Proteins, Papillomavirus Infections virology, Polymerase Chain Reaction, Tumor Virus Infections virology, Esophageal Neoplasms virology, Papillomaviridae genetics, Papillomavirus Infections epidemiology, Repressor Proteins, Tumor Virus Infections epidemiology
- Abstract
To investigate the potential role of human papillomavirus (HPV) infection in the pathogenesis of esophageal carcinomas in the Anyang area of China, we have evaluated specimens collected by balloon cytology examination from volunteers in two regions with significantly different incidences of esophageal carcinoma. 138 donors were from a village in a county with an esophageal carcinoma (EC) age-adjusted mortality rate of 132x10(5), the remaining 68 were resident in a second village from another county with an EC mortality rate of 52x10(5). Specimens were evaluated using both polymerase chain reaction (PCR) amplification and in situ hybridization (ISH) protocols. PCR results showed that the prevalence of the human papillomavirus type 16 (HPV-16) E6 gene in the high incidence area was 1.9-fold higher than that of the low incidence area (72 and 37%, respectively, P < 0.01). Moreover, the positive rate corresponded with pathology grade. Similar results were obtained with the HPV-16 E7 gene. As the cells undergoing cytopathological progress, the HPV-16 E6 positive rate was increased, in both villages. In contrast to HPV-16 E6 and E7, detection of the HPV L1 gene was consistently lower, and its prevalence decreased with increasing dysplasia grades (P < 0.05). By ISH analyses, the expression rate of HPV-16 E6 in the specimens collected from the high incidence area was 2.2-fold higher than those from the low incidence area (49 versus 22%, respectively; P < 0.05), and transcription of the E6 gene paralleled cytopathology. HPV-18 was also detected in 17 and 15% of the specimens from the high and low incidence areas, respectively, but most of these samples were also simultaneously HVP-16 positive. These results suggest that HVP-16 plays a causative role in the high incidence of esophageal cancer in the Anyang region of CHINA:
- Published
- 2001
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17. Reduced DNA-dependent protein kinase activity is associated with lung cancer.
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Auckley DH, Crowell RE, Heaphy ER, Stidley CA, Lechner JF, Gilliland FD, and Belinsky SA
- Subjects
- Adult, Aged, Bleomycin pharmacology, Case-Control Studies, Cell Survival drug effects, DNA-Activated Protein Kinase, Female, Humans, Lung Neoplasms pathology, Male, Middle Aged, Nuclear Proteins, DNA-Binding Proteins, Lung Neoplasms enzymology, Protein Serine-Threonine Kinases metabolism
- Abstract
Reduced DNA repair capacity of carcinogen-induced DNA damage is now thought to significantly influence inherent susceptibility to lung cancer. DNA-dependent protein kinase (DNA-PK) is a serine-threonine kinase activated by the presence of double-strand breaks in DNA that appears to play a major role in non-homologous recombination and transcriptional control. The purpose of this study was to determine whether DNA-PK activity varies among individuals and how this affects lung cancer risk. DNA-PK activity in peripheral mononuclear cells from individuals with lung cancer (n = 41) was compared with lung cancer-free controls (n = 41). Interindividual variability was seen within each group, however, significant differences (P = 0.03) in DNA-PK activity between cases and controls were seen when comparing the distribution of enzyme activity among these two groups. The percentages of cases and controls with DNA-PK activity in the ranges 2.5-5.0 and 7.6-10.0 units were 39 versus 20% and 7 versus 29%, respectively. The enzyme activity in peripheral mononuclear cells reflected that seen in bronchial epithelial cells, one progenitor cell for lung cancer, supporting the use of peripheral mononuclear cells for larger population-based studies of DNA-PK activity. Its role as a potential modifier for lung cancer risk was supported by the fact that cell growth in bronchial epithelial cells exposed to bleomycin was directly associated with enzyme activity. The results of this study demonstrate that reduced DNA-PK repair activity is associated with risk for lung cancer.
- Published
- 2001
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18. Perspective: cell differentiation theory may advance early detection of and therapy for lung cancer.
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Lechner JF, Fugaro JM, Wong Y, Pass HI, Harris CC, and Belinsky SA
- Subjects
- Genes, Homeobox, Humans, Lung Neoplasms genetics, Cell Differentiation genetics, Lung Neoplasms pathology, Lung Neoplasms therapy
- Abstract
Many of these deaths could be prevented if there were better screening methods to uncover the disease when it is limited and most responsive to intervention. Novel biomarkers of early-stage disease are therefore needed. By applying the principle of "oncology recapitulates ontogeny", we have discovered three homeobox (HOX) genes that are inappropriately expressed in the majority of lung tumors. Understanding the role of these inappropriately expressed genes in lung epithelial cell carcinogenesis may not only augment early detection, but may also offer new avenues of treatment of this disease.
- Published
- 2001
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19. A simple method for generating full length cDNA from low abundance partial genomic clones.
- Author
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Wang Y, Fugaro JM, Siddiq F, Goparaju CM, Lonardo F, Wali A, Lechner JF, and Pass HI
- Abstract
Background: PCR amplification of target molecules involves sequence specific primers that flank the region to be amplified. While this technique is generally routine, its applicability may not be sufficient to generate a desired target molecule from two separate regions involving intron /exon boundaries. For these situations, the generation of full-length complementary DNAs from two partial genomic clones becomes necessary for the family of low abundance genes., Results: The first approach we used for the isolation of full-length cDNA from two known genomic clones of Hox genes was based on fusion PCR. Here we describe a simple and efficient method of amplification for homeobox D13 (HOXD13) full length cDNA from two partial genomic clones. Specific 5' and 3' untranslated region (UTR) primer pairs and website program (primer3_www.cgv0.2) were key steps involved in this process., Conclusions: We have devised a simple, rapid and easy method for generating cDNA clone from genomic sequences. The full length HOXD13 clone (1.1 kb) generated with this technique was confirmed by sequence analysis. This simple approach can be utilized to generate full-length cDNA clones from available partial genomic sequences.
- Published
- 2000
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- View/download PDF
20. Frequency of trisomy 20 in nonmalignant bronchial epithelium from lung cancer patients and cancer-free former uranium miners and smokers.
- Author
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Neft RE, Crowell RE, Gilliland FD, Murphy MM, Lane JL, Harms H, Coons T, Heaphy E, Belinsky SA, and Lechner JF
- Subjects
- Adult, Aged, Aged, 80 and over, Biomarkers, Tumor, Cells, Cultured, Female, Humans, In Situ Hybridization, Fluorescence, Male, Middle Aged, Predictive Value of Tests, Bronchi cytology, Carcinoma, Non-Small-Cell Lung genetics, Carcinoma, Non-Small-Cell Lung prevention & control, Chromosomes, Human, Pair 20 genetics, Lung Neoplasms genetics, Lung Neoplasms prevention & control, Mining, Occupational Exposure adverse effects, Smoking adverse effects, Trisomy, Uranium adverse effects
- Abstract
Lung cancer is the leading cause of cancer-related deaths. The development of sensitive screening methods to identify at-risk individuals before emergence of clinical disease would permit early intervention that could decrease this mortality. Our previous studies have shown that cells with trisomy 7 can be detected in bronchial epithelium from cancer-free smokers and former uranium miners. However, the use of more than one molecular marker could increase the chance of identifying at-risk individuals. Trisomy 20, which is found in 43-57% of non-small cell lung cancers, is a candidate marker. The purpose of the current investigation was to determine the percentage of cells with trisomy 20 in persons with a high risk for lung cancer. Bronchial epithelial cells that had been assayed for trisomy 7 were assayed for trisomy 20 by fluorescence in situ hybridization. Trisomy 20 was detected in bronchial epithelial cells from lung cancer patients and from smokers and ex-uranium miners without lung cancer. In some cases, patients who were negative for trisomy 7 exhibited trisomy 20. Consequently, more people with field cancerization were identified using both markers. However, the two markers combined did not appear to stratify the risk for lung cancer.
- Published
- 1998
21. Carcinogenic responses of transgenic heterozygous p53 knockout mice to inhaled 239PuO2 or metallic beryllium.
- Author
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Finch GL, March TH, Hahn FF, Barr EB, Belinsky SA, Hoover MD, Lechner JF, Nikula KJ, and Hobbs CH
- Subjects
- Adenocarcinoma chemically induced, Adenocarcinoma pathology, Administration, Inhalation, Aging pathology, Animals, Beryllium administration & dosage, Body Burden, Carcinogenicity Tests, Carcinogens administration & dosage, Female, Lung pathology, Lung Neoplasms chemically induced, Lung Neoplasms pathology, Male, Mice, Mice, Knockout, Neoplasms, Experimental chemically induced, Neoplasms, Experimental pathology, Plutonium administration & dosage, Pneumonia chemically induced, Pneumonia pathology, Survival Analysis, Beryllium toxicity, Carcinogens toxicity, Genes, p53 genetics, Plutonium toxicity
- Abstract
The transgenic heterozygous p53+/- knockout mouse has been a model for assessing the tumorigenicity of selected carcinogens administered by noninhalation routes of exposure. The sensitivity of the model for predicting cancer by inhaled chemicals has not been examined. This study addresses this issue by acutely exposing p53+/- mice of both sexes by nose-only inhalation to either air (controls), or to 1 of 2 levels of 239PuO2 (500 or 100 Bq 239Pu) or beryllium (Be) metal (60 or 15 micrograms). Additional wild-type p53+/+ mice were exposed by inhalation to either 500 Bq of 239PuO2 or 60 micrograms of Be metal. These carcinogens were selected because they operate by differing mechanisms and because of their use in other pulmonary carcinogenesis studies in our laboratory. Four or 5 of the 15 mice per sex from each group were sacrificed 6 mo after exposure, and only 2 pulmonary neoplasms were observed. The remainder of the mice were held for life-span observation and euthanasia as they became moribund. Survival of the p53+/- knockout mice was reduced compared to the p53+/+ wild-type mice. No lung neoplasms were observed in p53+/- mice exposed to air alone. Eleven of the p53+/- mice inhaling 239PuO2 developed pulmonary neoplasms. Seven p53+/+ mice exposed to 239PuO2 also developed pulmonary neoplasms, but the latency period for pulmonary neoplasia was significantly shorter in the p53+/ mice. Four pulmonary neoplasms were observed in p53+/- mice exposed to the higher dose of Be, whereas none were observed in the wild-type mice or in the heterozygous mice exposed to the lower dose of Be. Thus, both p53+/- and p53+/+ mice were susceptible to 239Pu-induced carcinogenesis, whereas the p53+/- but not the p53+/+ mice were susceptible to Be-induced carcinogenesis. However, only 2 pulmonary neoplasms (1 in each of the 239PuO2 exposure groups) were observed in the 59 p53+/ mice that were sacrificed or euthanatized within 9 mo after exposure, indicating that the p53+/- knockout mouse might not be appropriate for a 6-mo model of carcinogenesis for these inhaled carcinogens.
- Published
- 1998
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22. Overexpression of hMTH1 mRNA: a molecular marker of oxidative stress in lung cancer cells.
- Author
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Kennedy CH, Cueto R, Belinsky SA, Lechner JF, and Pryor WA
- Subjects
- Adaptor Proteins, Signal Transducing, Fungal Proteins genetics, Humans, Lung Neoplasms metabolism, Tumor Cells, Cultured, Biomarkers, Tumor metabolism, Fungal Proteins metabolism, Membrane Proteins, Neoplasm Proteins metabolism, Oxidative Stress, RNA, Messenger metabolism, Saccharomyces cerevisiae Proteins
- Abstract
Human MutT homologue (hMTH1) mRNA was overexpressed in SV-40-transformed non-tumorigenic human bronchial epithelial cells (BEAS-2B cells) and in 11 out of 12 human lung cancer cell lines relative to normal human bronchial epithelial cells. Expression levels of hMTH1 mRNA were inversely proportional to cellular levels of 8-oxo-deoxyguanosine. Together, these results suggest that hMTH1 gene expression may represent a molecular marker of oxidative stress that could ultimately be used to elucidate the temporal relationships between oxidative stress, genomic instability and the development of lung cancer.
- Published
- 1998
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23. A canine model of familial mammary gland neoplasia.
- Author
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Schafer KA, Kelly G, Schrader R, Griffith WC, Muggenburg BA, Tierney LA, Lechner JF, Janovitz EB, and Hahn FF
- Subjects
- Animals, Biomarkers, Tumor metabolism, Dog Diseases metabolism, Dog Diseases pathology, Dogs, Female, Immunohistochemistry, Incidence, Male, Mammary Neoplasms, Animal metabolism, Mammary Neoplasms, Animal pathology, Pedigree, Receptor, ErbB-2 metabolism, Risk Factors, Tumor Suppressor Protein p53 metabolism, Disease Models, Animal, Dog Diseases genetics, Mammary Neoplasms, Animal genetics
- Abstract
Intact female Beagles from life-span studies in the Lovelace Respiratory Research Institute colony were examined for mammary tumor incidence. The breeding colony, founded in 1963, produced five generations from 28 founder females. After proportional hazards analysis, two maternal families were shown to have markedly different phenotypes, one susceptible and one resistant to mammary neoplasia, as compared with the entire colony. When tumors were subdivided into benign and malignant based on local invasiveness, familial differences in tumor incidence were preserved for each tumor type. Fifty-seven females in the susceptible family developed 149 benign and 39 malignant tumors, and 95 females in the resistant family developed 70 benign and 20 malignant tumors. The ratio of benign to malignant tumors of about 4:1 for both families was higher than expected. Using Kaplan-Meier and log-rank analyses, the susceptible family had a 50% malignant tumor incidence by age 13.6 years, whereas the resistant family did not have a 50% incidence until 17.0 years (P = 0.0065). Because of marked censoring, Kaplan-Meier analyses could not provide an estimate of the 50% benign tumor incidence; mean incidence age was calculated instead. These estimates for benign tumors for susceptible and resistant families were 10.8 and 13.8 years (P = 0.0001), respectively. Using chi(2) tests, families had no differences in the occurrence of the types of benign (P = 0.098) or malignant (P = 0.194) tumors or in the ratio of benign to malignant tumors (P = 0.778). Immunohistochemical analysis of malignant tumors from both families did not demonstrate differences in p53 mutation rate or p185erbB-2 expression. These results suggest that 1) genetic factors produce familial differences in the age of onset of both benign and malignant mammary tumors; histologic types do not segregate by family; 2) the ratio of benign to malignant tumors is greater than formerly reported; and 3) neither p53 nor p185erbB-2 alterations are the basis for the familial predisposition.
- Published
- 1998
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24. Individuals at high risk for lung cancer have airway epithelial cells with chromosome aberrations frequently found in lung tumor cells.
- Author
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Lechner JF, Neft RE, Gilliland FD, Crowell RE, Auckley DH, Temes RT, and Belinsky SA
- Subjects
- Cells, Cultured, Epithelial Cells, Humans, In Situ Hybridization, Fluorescence, Lung Neoplasms pathology, Risk Factors, Trisomy, Tumor Cells, Cultured, Bronchi pathology, Chromosome Aberrations, Lung Neoplasms genetics
- Abstract
Identification of individuals at greatest risk of developing lung cancer could enhance the efficacy of intervention modalities, thereby greatly reducing mortality from this disease. One strategy for identifying these people is to establish molecular markers which reflect the severity of their cancerization field. Thus, investigations were initiated to determine of cells with chromosome aberrations frequently exhibited by lung tumor cells, i.e., trisomy 7, trisomy 20, and deletion of 9p23, are prevalent within the uninvolved airways of cancer patients. As a result, cells containing these aberrations were consistently found at significantly elevated levels by using fluorescence in situ hybridization (FISH). In contrast, cells collected from non-smokers who had never smoked were normal by this assay. The next objective was to determine of cells exhibiting these alterations are also present in upper airways of exposed, but cancer-free smokers and ex-uranium miners. The results showed that, although only a subset of these people will develop lung cancer in their lifetimes, they universally harbor increased numbers of abnormal cells within their airway epithelium. However, the number of sites with multiple verities of abnormal cells tended to be fewer compared with the cancer patients. Thus, quantifying cells with molecular alterations within the cancerization field of a smoker may delineate those with a lesser grade of damage, and these individuals may be at a lesser risk of developing disease. However, differences in the extent of genetic damage afforded by these assays may not clearly define individuals with pending disease, and additional molecular assays must be devised.
- Published
- 1998
25. Concurrent fluorescence in situ hybridization and immunocytochemistry for the detection of chromosome aberrations in exfoliated bronchial epithelial cells.
- Author
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Neft RE, Murphy MM, Tierney LA, Belinsky SA, Anderson M, Saccomanno G, Michels R, Timm S, Gilliland FD, Crowell RE, and Lechner JF
- Subjects
- Antibodies, Monoclonal, DNA, Satellite, Epithelial Cells pathology, Humans, Immunohistochemistry methods, In Situ Hybridization, Fluorescence methods, Reproducibility of Results, Sensitivity and Specificity, Bronchi pathology, Chromosome Aberrations, Chromosomes, Human, Pair 7, Lung Neoplasms genetics, Lung Neoplasms pathology, Sputum cytology
- Abstract
Objective: A procedure was developed to allow concurrent detection of chromosome aberrations and identification of bronchial epithelial cells., Study Design: Fluorescence in situ hybridization for chromosome 7 and immunocytochemistry for cytokeratin were performed on exfoliated bronchial epithelial cells in a sputum sample from a cancer patient., Results: The Spectrum Orange-labeled alpha satellite probe for chromosome 7 produced red fluorescence, nuclei were counterstained with 4,6-diamidino-2-phenylindole (blue), and cytokeratin was visualized using a fluorescein isothiocyanate (FITC)-conjugated secondary antibody (green)., Conclusion: This procedure allowed the rapid identification of airway epithelial cells with numerical chromosome aberrations in this sample. Ultimately, this procedure could increase the sensitivity and specificity of sputum cytology as a laboratory diagnostic tool for the early detection of lung cancer.
- Published
- 1997
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26. Oncogenes and tumor-suppressor genes in mesothelioma--a synopsis.
- Author
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Lechner JF, Tesfaigzi J, and Gerwin BI
- Subjects
- Carcinogens toxicity, Cell Physiological Phenomena, Genes, Tumor Suppressor genetics, Humans, Oncogenes genetics, Genes, Tumor Suppressor physiology, Mesothelioma genetics, Oncogenes physiology
- Abstract
Invariably mesothelioma is diagnosed late in the development of the disease when treatment is no longer effective. Therefore, a key to reducing the mortality rate of this neoplasm is knowledge of the general sequence of genetic events between initiation of mesothelial cells and the emergence of the metastatic tumor cells. Unfortunately, relatively little is known about the early changes in the genesis of this disease. Of the known changes, the most frequent are in the tumor-suppressor genes p16INK4a and NF2 and possibly the SV40 virus large T-antigen oncogene. The molecular nature of the changes in these genes as well as other alterations are addressed in this overview.
- Published
- 1997
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27. Radon and lung carcinogenesis: mutability of p53 codons 249 and 250 to 238Pu alpha-particles in human bronchial epithelial cells.
- Author
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Hussain SP, Kennedy CH, Amstad P, Lui H, Lechner JF, and Harris CC
- Subjects
- Adolescent, Codon genetics, Genes, p53 genetics, Humans, Male, Mutagenicity Tests, Codon radiation effects, Genes, p53 radiation effects, Lung Neoplasms genetics, Mutagenesis, Neoplasms, Radiation-Induced genetics, Radon toxicity
- Abstract
Radon-222, a decay product of uranium-238 and a source of high linear energy transfer (LET) alpha-particles, has been implicated in the increased risk of lung cancer in uranium miners as well as non-miners. p53 mutation spectrum studies of radon-associated lung cancer have failed to show any specific mutational hot spot with the exception of a single study in which 31% of squamous cell and large cell lung cancers from uranium miners showed a p53 codon 249 AGGarg --> ATGmet mutation. Although the results of laboratory studies indicate that double-strand breaks and deletions are the principal genetic alterations caused by alpha-particles, uncertainty still prevails in the description of DNA damage in radon-associated human lung cancer. In the present study, we have evaluated the mutability of p53 codons 249 and 250 to alpha-particles in normal human bronchial epithelial (NHBE) cells using a highly sensitive genotypic mutation assay. Exposure of NHBE cells to a total dose of 4 Gy (equivalent to approximately 1460 working level months in uranium mining) of high LET alpha-radiation induced codon 249 AGG --> AAG transitions and codon 250 CCC --> ACC transversions with absolute mutation frequencies of 3.6 x 10(-7) and 3.8 x 10(-7) respectively. This mutation spectrum is consistent with our previous report of radon-associated human lung cancer.
- Published
- 1997
- Full Text
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28. Molecular identification of individuals at high risk for lung cancer.
- Author
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Lechner JF, Neft RE, Gilliland FD, Crowell RE, and Belinsky SA
- Subjects
- Bronchoscopy, Cells, Cultured, Chromosomes, Human, Pair 2 genetics, Chromosomes, Human, Pair 7 genetics, Epithelium pathology, Humans, In Situ Hybridization, Fluorescence, Lung Neoplasms etiology, Lung Neoplasms pathology, Mining, Molecular Biology, Ploidies, Precancerous Conditions genetics, Precancerous Conditions pathology, Radon adverse effects, Risk Factors, Smoking genetics, Smoking pathology, Trisomy, Uranium adverse effects, Bronchi pathology, Lung Neoplasms genetics
- Abstract
The objective of the work reviewed herein was to evaluate whether a cancerization field-consisting of cells with genetic alterations can be detected within normal-appearing bronchial epithelium. By using fluorescence in situ hybridization (FISH) for trisomy 7, cancerization fields were detected in the majority of cancer patients and also in significant percentages of cancer-free tobacco smokers and former uranium miners. These results suggest that molecular analyses may enhance the power of detecting premalignant changes in bronchial epithelium and may ultimately lead to identifying persons at greatest risk for developing lung cancer.
- Published
- 1997
- Full Text
- View/download PDF
29. Chromosomal changes and progressive tumorigenesis of human bronchial epithelial cell lines.
- Author
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Ohnuki Y, Reddel RR, Bates SE, Lehman TA, Lechner JF, and Harris CC
- Subjects
- Animals, Bronchi, Cell Line, Chromosome Banding, Chromosome Mapping, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 21, Chromosomes, Human, Pair 22, Chromosomes, Human, Pair 8, Culture Techniques methods, Epithelium, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Lung Neoplasms pathology, Mice, Mice, Nude, Simian virus 40, Transplantation, Heterologous, Cell Transformation, Neoplastic, Chromosome Aberrations, Chromosome Disorders, Lung Neoplasms genetics
- Abstract
A simian virus 40 (SV40)-transformed human bronchial epithelial cell line, BEAS-2B, underwent progressive changes, including the development of tumorigenicity, during extended in vitro passaging. Karyotypic changes occurred in parallel with the phenotypic changes. For the first 12 passages following viral transformation, there were random karyotypic changes. Immortalization occurred between passages 12 and 21, corresponding with the accumulation of four characteristic abnormal chromosomes-m-1: add(15)(p11.1); m-2: der(8;9)(q10;q10); m-3: add(16)(p13); and m-4: mar4- and the loss of one homolog of chromosomes 8, 15, 16, 21, and 22. With further passaging (from 21 to 63), the acquisition of weak tumorigenicity was observed, accompanied by an increased frequency of cells containing all four common abnormal chromosomes, m-1 through m-4, and missing one normal homolog of chromosomes 8, 15, 16, and 22. Four tumor cell lines (B39-TL, B39-TR, B61-T4 and B61-T7) were established from tumors induced by the injection of these weakly tumorigenic BEAS-2B 39th- and 61st- passage cells into athymic nude mice. One of the cell lines, B39-TL, is significantly more tumorigenic than the others. It is notable that B39-TL showed two specific abnormal chromosomes, del(3p);der(3;15) (q10;q10) and m-6; der(21)t(3;21)(p14.2;p12) inducing deletion of a short arm of chromosome 3. Fluorescence in situ hybridization analysis with a probe for protein tyrosine phosphatase-gamma demonstrated loss of heterozygosity in the 3p14 region. The development of step-wise karyotypic changes in this in vitro carcinogenesis model parallels changes documented in several common human cancers.
- Published
- 1996
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30. Induction of EGF receptor and erbB-2 during endotoxin-induced alveolar type II cell proliferation in the rat lung.
- Author
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Tesfaigzi J, Johnson NF, and Lechner JF
- Subjects
- Animals, Blotting, Western, Bronchoalveolar Lavage Fluid cytology, Hyperplasia etiology, Hyperplasia metabolism, Hyperplasia pathology, Immunoenzyme Techniques, Macrophages, Alveolar pathology, Male, Neutrophils pathology, Pulmonary Alveoli metabolism, Pulmonary Alveoli ultrastructure, Rats, Rats, Inbred F344, ErbB Receptors metabolism, Escherichia coli, Lipopolysaccharides toxicity, Pulmonary Alveoli pathology, Receptor, ErbB-2 metabolism
- Abstract
The overall purpose of this study was to produce a model of transient type II cell hyperplasia to enable comparisons of changes in gene expression in the remodelling epithelium with those in carcinogen-induced hyperplastic lesions. Rats instilled with endotoxin had increased numbers of neutrophils in the bronchoalveolar lavage fluid (BALF) by 3 hours that reached maximum levels at 48 hours and returned to background levels 168 hours after instillation. The number of macrophages in the BALF increased throughout the 168 hours following instillation. Epithelial cell hyperplasia was maximum at 96 hours post-instillation in areas of extensive inflammation. The number of alveolar epithelial cells that exhibited bromodeoxyuridine nuclear incorporation reached maximum levels 48 hours after endotoxin treatment and decreased to near background levels at 96 hours. Ultrastructural studies of hyperplastic cells showed the presence of lamellar bodies and condensed chromosomes, characteristics of type II cells in mitosis. At 168 hours after instillation, the hyperplasia regressed to form normal-appearing alveolar structure with few focal lesions. Specific immunostaining for the proto-oncogenes, EGF receptor and erbB-2, on tissue sections increased during the endotoxin-induced hyperplasia. Furthermore, the induction of the 170 kDa and 180 kDa glycoproteins in type II cells isolated from endotoxin-instilled rats was shown by Western analysis. These proto-oncogenes, often thought to be markers of early events during neoplasia, may, therefore, also be associated with wound repair mechanisms after hyperplasia.
- Published
- 1996
- Full Text
- View/download PDF
31. Detection of trisomy 7 in nonmalignant bronchial epithelium from lung cancer patients and individuals at risk for lung cancer.
- Author
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Crowell RE, Gilliland FD, Temes RT, Harms HJ, Neft RE, Heaphy E, Auckley DH, Crooks LA, Jordan SW, Samet JM, Lechner JF, and Belinsky SA
- Subjects
- Aged, Aneuploidy, Cytodiagnosis, Epithelium pathology, Genetic Markers, Humans, Hyperplasia, In Situ Hybridization, Fluorescence, Lung Neoplasms pathology, Middle Aged, Mining, Precancerous Conditions pathology, Risk Factors, Smoking, Bronchi pathology, Chromosomes, Human, Pair 7 genetics, Lung Neoplasms genetics, Precancerous Conditions genetics, Trisomy genetics
- Abstract
Early identification and subsequent intervention are needed to decrease the high mortality rate associated with lung cancer. The examination of bronchial epithelium for genetic changes could be a valuable approach to identify individuals at greatest risk. The purpose of this investigation was to assay cells recovered from nonmalignant bronchial epithelium by fluorescence in situ hybridization for trisomy of chromosome 7, an alteration common in non-small cell lung cancer. Bronchial epithelium was collected during bronchoscopy from 16 cigarette smokers undergoing clinical evaluation for possible lung cancer and from seven individuals with a prior history of underground uranium mining. Normal bronchial epithelium was obtained from individuals without a prior history of smoking (never smokers). Bronchial cells were collected from a segmental bronchus in up to four different lung lobes for cytology and tissue culture. Twelve of 16 smokers were diagnosed with lung cancer. Cytological changes found in bronchial epithelium included squamous metaplasia, hyperplasia, and atypical glandular cells. These changes were present in 33, 12, and 47% of sites from lung cancer patients, smokers, and former uranium miners, respectively. Less than 10% of cells recovered from the diagnostic brush had cytological changes, and in several cases, these changes were present within different lobes from the same patient. Background frequencies for trisomy 7 were 1.4 +/- 0.3% in bronchial epithelial cells from never smokers. Eighteen of 42 bronchial sites from lung cancer patients showed significantly elevated frequencies of trisomy 7 compared to never smoker controls. Six of the sites positive for trisomy 7 also contained cytological abnormalities. Trisomy 7 was found in six of seven patients diagnosed with squamous cell carcinoma, one of one patient with adenosquamous cell carcinoma, but in only one of four patients with adenocarcinoma. A significant increase in trisomy 7 frequency was detected in cytologically normal bronchial epithelium collected from four sites in one cancer-free smoker, whereas epithelium from the other smokers did not contain this chromosome abnormality. Finally, trisomy 7 was observed in almost half of the former uranium miners; three of seven sites positive for trisomy 7 also exhibited hyperplasia. Two of the former uranium miners who were positive for trisomy 7 developed squamous cell carcinoma 2 years after collection of bronchial cells. To determine whether the increased frequency of trisomy 7 reflects generalized aneuploidy or specific chromosomal duplication, a subgroup of samples was evaluated for trisomy of chromosome 2; the frequency was not elevated in any of the cases as compared with controls. The studies described in this report are the first to detect and quantify the presence of trisomy 7 in subjects at risk for lung cancer. These results also demonstrate the ability to detect genetic changes in cytologically normal cells, suggesting that molecular analyses may enhance the power for detecting premalignant changes in bronchial epithelium in high-risk individuals.
- Published
- 1996
32. Induction of genomic instability in normal human bronchial epithelial cells by 238Pu alpha-particles.
- Author
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Kennedy CH, Mitchell CE, Fukushima NH, Neft RE, and Lechner JF
- Subjects
- Adolescent, Bronchi cytology, Cell Division radiation effects, Cells, Cultured, DNA, Satellite, Dose-Response Relationship, Radiation, Epithelial Cells, Epithelium radiation effects, Humans, Male, Alpha Particles, Bronchi radiation effects, Mutation, Polonium
- Abstract
Pulmonary deposition of alpha-particle-emitting radon daughters is estimated to account for 10% of all lung cancer deaths in the USA. However, the nature and timing of early (preneoplastic) genetic alterations in radon-associated lung cancer are still relatively uncertain. The purpose of this investigation was to determine whether genomic instability occurs after exposure of cultured normal human bronchial epithelial cells to six equal, fractionated doses of alpha-particles (total doses 2-4 Gy). Two weeks after the final exposure, foci of phenotypically altered cells (PACs) were detected in 0, 63 and 77% of control, low and high dose cultures respectively. Of these, 18% exhibited extended life spans relative to unexposed controls. Elevated frequencies of binucleated cells (BNCs), a marker of genomic instability, were observed in 60 and 38% of the PAC cultures from the low and high dose groups respectively. The micronucleus assay also showed evidence of genomic instability in 40 and 38% of PAC cultures from the low dose and high dose groups respectively. No changes in microsatellite length, another marker of genomic instability, were detected in any of the PAC samples with the 28 markers used for this assay. However, one PAC (L2) showed a hemizygous deletion at 9p13.3. Another PAC (H9), which exhibited the highest frequency of cells containing micronuclei (MN), exhibited a hemizygous deletion at 7q31.3. Each loss may represent a stable mutation that resulted either directly from irradiation or later in progeny of exposed cells because of alpha-particle-induced genomic instability. The fact that elevated levels of BNCs and MN were present in the progeny many generations after irradiation indicates that the genetic alterations detected with these two markers were not a direct consequence of radiation exposure, but of resulting genomic instability, which may be an early change after exposure to alpha-particles.
- Published
- 1996
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33. Failure of cigarette smoke to induce or promote lung cancer in the A/J mouse.
- Author
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Finch GL, Nikula KJ, Belinsky SA, Barr EB, Stoner GD, and Lechner JF
- Subjects
- Analysis of Variance, Animals, Body Weight, Carboxyhemoglobin metabolism, Carcinogens, Female, Lung anatomy & histology, Lung pathology, Lung Neoplasms chemically induced, Mice, Mice, Inbred A, Nitrosamines, Organ Size, Reference Values, Survival Analysis, Lung Neoplasms pathology, Smoke adverse effects, Smoking adverse effects
- Abstract
A six-month bioassay in A/J mice was conducted to test the hypothesis that chronically inhaled mainstream cigarette smoke would either induce lung cancer or promote lung carcinogenicity induced by the tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). Groups of 20 female A/J mice were exposed to filtered air (FA) or cigarette smoke (CS), injected with NNK, or exposed to both CS and NNK. At 7 weeks of age, mice were injected once with NNK; 3 days later, they were exposed to CS for 6 h/day, 5 days/week, for 26 weeks at a mean 248 mg total particulate matter/m3 concentration. Animals were sacrificed 5 weeks after exposures ended for gross and histological evaluation of lung lesions. No significant differences in survival between exposure groups was observed. A biologically significant level of CS exposure was achieved as indicated by CS-induced body weight reductions, lung weight increases, and carboxyhemoglobin levels in blood of about 17%. Crude tumor incidences, as determined from gross observation of lung nodules, were similar between the CS-exposed and FA groups, and the NNK and CS + NNK groups. Incidences in either of these latter groups were greater than either the CS or FA groups. Furthermore, tumor multiplicity in tumor-bearing animals was not significantly different among any of the three groups (FA, NNK, CS + NNK) in which tumors were observed. Thus, CS exposure neither induced lung tumors nor promoted NNK-induced tumors. Because the CS exposure concentration was probably near the maximally tolerable level, longer exposures should be evaluated to potentially establish a CS-induced model of lung carcinogenesis in the A/J mouse.
- Published
- 1996
- Full Text
- View/download PDF
34. p53, erbB-2 and K-ras gene alterations are rare in spontaneous and plutonium-239-induced canine lung neoplasia.
- Author
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Tierney LA, Hahn FF, and Lechner JF
- Subjects
- Alpha Particles, Animals, Cells, Cultured, Dogs, Immunoenzyme Techniques, Lung radiation effects, Plutonium, Proto-Oncogene Mas, Trachea cytology, Genes, erbB-2, Genes, p53, Genes, ras, Lung Neoplasms genetics, Neoplasms, Radiation-Induced genetics, Receptor, ErbB-2 metabolism, Tumor Suppressor Protein p53 metabolism
- Abstract
Inhalation of high-linear energy transfer radiation in the form of radon progeny is a suspected cause of human lung cancer. To gain insight into the types of genetic derangement(s) caused by this type of radiation, lung tumors from beagle dogs exposed to 239PuO2 and those arising in animals with no known carcinogen exposure were examined for evidence of aberrations in genes known to be altered in lung tumors. Altered expression of the p53 tumor suppressor gene and proto-oncogene erbB-2 proteins (p185erbB2) was evaluated by immunohistochemical analysis of 117 tumors representing different histological types in exposed (n = 80) and unexposed (n = 37) animals. Twenty-eight tumors were analyzed for K-ras proto-oncogene mutations by polymerase chain reaction amplification and direct sequencing. Fourteen percent (16/116) of all lung neoplasms showed elevated nuclear accumulation of p53 protein. Regardless of exposure history, adenosquamous and squamous cell cancers comprised 94% of all tumors with p53 abnormalities. Eighteen percent (21/117) of all tumors had evidence in codons 12, 13 or 61 tumors from unexposed (n = 9) or plutonium-exposed dogs (n = 19). These data indicate that p53 and K-ras gene abnormalities as a result of missense mutation are infrequent events in spontaneous and 239PuO2-induced lung neoplasia in this colony of beagle dogs. Alternative mechanisms of gene alteration may be involved in canine pulmonary carcinogenesis.
- Published
- 1996
35. An improved method for the isolation of type II and Clara cells from mice.
- Author
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Belinsky SA, Lechner JF, and Johnson NF
- Subjects
- Animals, Barium, Bronchoalveolar Lavage Fluid, Cell Count, Cell Size, Cells, Cultured, Centrifugation methods, Culture Media, Female, Fibroblast Growth Factor 1, Male, Mice, Mice, Inbred A, Phagocytosis, Bronchi cytology, Cell Separation methods, Lung cytology, Pulmonary Alveoli cytology
- Abstract
Identifying the causal events and temporal aspects of lung cancer development requires the ability to isolate target and nontarget cells for comparative analyses. Current methodology can either isolate only one pure specific cell population from a lung or multiple cell types at lower purity. Previous studies in our laboratory have identified the alveolar type II cell as the progenitor cell for tumor development in the A/J mouse. The purpose of this study was to develop new protocols for the isolation and culture of type II and Clara cells from the mouse lung. Both type II and Clara cells were obtained in high purity using a sequential centrifugal elutriation protocol. In the first elutriation, cell fractions were collected using a Standard chamber. The type II and Clara cell fractions were then elutriated separately (two different separations) using a Sanderson chamber. The final purity of the type II and Clara cell preparations was 73% and 76%, respectively. Colonies of 4 to 20 Clara cells exhibiting epithelial morphology were evident 1 wk after plating in low serum medium. The growth of type II cells required the addition of bronchioalveolar lavage fluid and acidic fibroblast growth factor to the medium. The isolation of viable mouse type II and Clara cells in high purity should facilitate the identification of cell-specific changes in gene expressions or in enzymatic pathways following in vivo or in vitro exposure to environmental carcinogens.
- Published
- 1995
- Full Text
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36. Detection and quantitation of mutant K-ras codon 12 restriction fragments by capillary electrophoresis.
- Author
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Mitchell CE, Belinsky SA, and Lechner JF
- Subjects
- Base Sequence, Cell Line, Deoxyribonucleases, Type II Site-Specific pharmacology, Electrophoresis, Molecular Sequence Data, Mutation, Polymerase Chain Reaction, Codon, Genes, ras
- Abstract
Polymerase chain reaction amplification and BstNI endonuclease digestion were performed on DNA isolated from cell lines that were either homozygous (SW480, A549) or heterozygous (Calu 1, SK-LU-1, A427) for K-ras codon 12 mutations. Polyacrylamide gel electrophoresis showed that both mutant and wildtype (WT) bands were present in Calu-1, SK-LU-1, and A427 cell DNA; only the mutant bands were observed with SW480 and A549 DNA. The percentages of mutant and WT fragments were measured using capillary electrophoresis (CE). Integration of mutant and WT peaks showed that the percentages of mutant alleles in Calu-1, SK-LU-1, and A427 cell lines were 73, 84, and 72, respectively. The sensitivity of the original BstNI assay for K-ras codon 12 in conjunction with analysis by CE was also tested by a series of titration experiments using one- and two-stage amplification-BstNI digestion protocols. CE was used to generate a calibration curve. The mutant allele was detected and the quantity was measured in the 1:100 and 1:10,000 dilutions in the one- and two-stage analysis, respectively. Four human lung adenocarcinomas were also analyzed. Two of these were homozygous normal, whereas the other two contained 63 and 32% codon 12 mutant alleles. These results showed that CE can separate and quantitate BstNI fragments containing K-ras codon 12 mutations. The high sensitivity and quantitative features of CE should enable detection and quantitation of mutant K-ras alleles in premalignant lung lesions, as well as exfoliated cells collected by cytology from persons at risk for lung cancer.(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1995
- Full Text
- View/download PDF
37. Alpha-particle-induced p53 protein expression in a rat lung epithelial cell strain.
- Author
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Hickman AW, Jaramillo RJ, Lechner JF, and Johnson NF
- Subjects
- Animals, Cells, Cultured, DNA Damage, Dose-Response Relationship, Radiation, Epithelium metabolism, Epithelium radiation effects, Lung radiation effects, Male, Plutonium, Rats, Rats, Inbred F344, Time Factors, Tumor Suppressor Protein p53 radiation effects, Alpha Particles, Lung metabolism, Tumor Suppressor Protein p53 biosynthesis
- Abstract
Other investigators have shown that both sparsely ionizing and UV radiation cause cell cycle arrest that is associated with increased expression of wild-type p53 protein. The effect of exposure to alpha-particles from 238Pu on the induction of the p53 protein has now been examined in cultured lung epithelial cells derived from male F344 rats. The number of cells having increased levels of p53 protein was determined by flow cytometry after the cells had been stained with a monoclonal antibody to p53. alpha-Particle irradiation caused a dose-dependent increase in p53 protein levels detectable at doses as low as 0.6 cGy, with no evidence of a threshold. An increase in p53 protein also occurred in X-irradiated cells. However, no increase was seen in cells exposed to less than 10 cGy of X-rays, indicating the existence of a relatively higher DNA damage threshold for sparsely ionizing radiation. In addition, more cells exposed to low doses of alpha radiation had increased p53 protein levels than would be predicted based on the number of nuclei expected to be traversed by an alpha-particle, suggesting that alpha-particles cause genetic damage by mechanisms in addition to direct interactions with DNA.
- Published
- 1994
38. Development of tumorigenicity in simian virus 40-immortalized human bronchial epithelial cell lines.
- Author
-
Reddel RR, Salghetti SE, Willey JC, Ohnuki Y, Ke Y, Gerwin BI, Lechner JF, and Harris CC
- Subjects
- Animals, Base Sequence, Bronchi pathology, Cell Line, Chromosome Aberrations, Epithelium pathology, Humans, Mice, Molecular Sequence Data, Neoplasms, Experimental pathology, Polymorphism, Restriction Fragment Length, Bronchial Neoplasms etiology, Cell Transformation, Neoplastic, Cell Transformation, Viral, Neoplasms, Experimental etiology, Simian virus 40 genetics
- Abstract
Of five SV40-transformed clonal human bronchial epithelial cell lines previously shown to be nontumorigenic at early passages (R. R. Reddel et al., Cancer Res., 48: 1904-1909, 1988), two lines (BES-1A1 and BEAS-2B) from different donors have become weakly tumorigenic with further passaging. BES-1A1 passage 26 cells formed tumors in 3 of 9 athymic nude mice given s.c. injections, whereas BEAS-2B cells of > or = 32 passages formed highly cystic tumors at 8 of 58 injection sites after long latency periods [17 +/- 7 (SD) weeks]. These tumors took a total of 36 +/- 8 weeks to reach a diameter of 1.0 cm. Tumor cell lines were established from four BEAS-2B tumors, and these are resistant to the growth-inhibitory effects of serum, an inducer of squamous differentiation in BEAS-2B and normal bronchial epithelial cells. This finding supports the hypothesis that development of resistance to inducers of terminal squamous differentiation may be a step in the process of bronchial carcinogenesis. One of these tumor cell lines, B39-TL, is significantly more tumorigenic than the others and has a deletion from the short arm of chromosome 3 as has been described previously for some naturally occurring human bronchial carcinomas. Thus, from the clonally derived BEAS-2B cell line, cell populations with various degrees of tumorigenicity have developed. Analysis of the changes in these cells may yield insights into the multiple events involved in acquisition of the tumorigenic phenotype.
- Published
- 1993
39. Tumorigenic conversion of human mesothelial cells as a consequence of platelet-derived growth factor-A chain overexpression.
- Author
-
Van der Meeren A, Seddon MB, Betsholtz CA, Lechner JF, and Gerwin BI
- Subjects
- Animals, Cells, Cultured, Epithelial Cells, Epithelium enzymology, Gene Expression, Humans, Isoenzymes metabolism, Karyotyping, Mice, Mice, Nude, Neoplasms, Experimental etiology, Precipitin Tests, RNA, Messenger genetics, Transfection, Tumor Cells, Cultured, Cell Transformation, Neoplastic, Platelet-Derived Growth Factor genetics
- Abstract
Overexpression of platelet-derived growth factor (PDGF)-A as well as PDGF-B chain mRNA has previously been reported in human mesothelioma cell lines. In this report, it has been established that the A but not the B chain protein is expressed at detectable levels in cell lysates and conditioned medium from these cell lines. In order to investigate the effect of overexpression of PDGF-A chain in a human mesothelial cell model system, a retroviral vector containing a human PDGF-A chain cDNA insert under the control of the Moloney murine leukemia virus (MoMLV) promoter was inserted into the SV-40 T-antigen immortalized human mesothelial cell line MeT-5A. Selected cells showed overexpression of PDGF-A chain relative to MeT-5A and induced tumors in athymic nude mice. PDGF-A chain overexpression was also found in the tumor specimens excised from the mice. PDGF-A mRNA and protein were expressed at a higher level in the tumor explant cell lines, suggesting a correlation of tumorigenicity with A chain production.
- Published
- 1993
- Full Text
- View/download PDF
40. Mutant p53 can induce tumorigenic conversion of human bronchial epithelial cells and reduce their responsiveness to a negative growth factor, transforming growth factor beta 1.
- Author
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Gerwin BI, Spillare E, Forrester K, Lehman TA, Kispert J, Welsh JA, Pfeifer AM, Lechner JF, Baker SJ, and Vogelstein B
- Subjects
- Animals, Cell Division drug effects, Genes, p53, Humans, In Vitro Techniques, Mice, Mice, Nude, Neoplasm Transplantation, Transfection, Tumor Cells, Cultured, Carcinoma, Bronchogenic pathology, Transforming Growth Factor beta pharmacology, Tumor Suppressor Protein p53 genetics
- Abstract
Loss of normal functions and gain of oncogenic functions when the p53 tumor suppressor gene is mutated are considered critical events in the development of the majority of human cancers. Human bronchial epithelial cells (BEAS-2B) provide an in vitro model system to study growth, differentiation, and neoplastic transformation of progenitor cells of lung carcinoma. When wild-type (WT) or mutant (MT; codon 143Val-Ala) human p53 cDNA was transfected into nontumorigenic BEAS-2B cells, we observed that (i) transfected WT p53 suppresses and MT p53 enhances the colony-forming efficiency of these cells, (ii) MT p53 increases resistance to transforming growth factor beta 1, and (iii) clones of MT p53 transfected BEAS-2B cells are tumorigenic when inoculated into athymic nude mice. These results are consistent with the hypothesis that certain mutations in p53 may function in multistage lung carcinogenesis by reducing the responsiveness of bronchial epithelial cells to negative growth factors.
- Published
- 1992
- Full Text
- View/download PDF
41. Cell density governs the ability of human bronchial epithelial cells to recognize serum and transforming growth factor beta-1 as squamous differentiation-inducing agents.
- Author
-
Ke Y, Gerwin BI, Ruskie SE, Pfeifer AM, Harris CC, and Lechner JF
- Subjects
- Autoradiography, Bronchi chemistry, Bronchi cytology, Cell Count, Cell Cycle, Cell Line drug effects, Colony-Forming Units Assay, DNA biosynthesis, Epithelial Cells, Epithelium drug effects, Humans, Protein Precursors analysis, Bronchi drug effects, Cell Differentiation drug effects, Fetal Blood, Transforming Growth Factor beta pharmacology
- Abstract
Sparse (75 to 2000 cells/cm2) density cultures of normal human bronchial epithelial cells uniformly undergo terminal squamous differentiation when incubated in medium containing serum (fetal bovine serum [FBS]) or transforming growth factor beta-1 (TGF-beta 1). It was found that the cell density of the culture affects the probability that a cell will respond to these differentiation-inducing agents. Thus whereas irreversible inhibition of DNA synthesis occurs in sparse cell-density cultures within 24 hours after exposure, only a transient (less than 36 hours) depression in DNA synthesis was seen in high (more than 10,000 cells/cm2) density cultures. In addition, although phase microscopic image analysis revealed that virtually all of the cells displayed a squamous morphology within 1 hour after exposure to FBS or TGF-beta 1, observations made 48 to 72 hours later showed the presence of clusters of small prolate spheroid-shaped cells surrounded by many involucrin-positive squamous-appearing cells. Only the small cells were capable of DNA synthesis and cell division as determined by autoradiography and time-lapse photomicrographic images. These replicating cells immediately undergo squamous differentiation if they are subcultured and reinoculated at low cell density and incubated in medium supplemented with FBS or TGF-beta 1. Therefore the probability that a human bronchial epithelial cell will be refractive to FBS- or TGF-beta 1 induced terminal squamous differentiation is solely a function of the cell density of the culture.
- Published
- 1990
42. TGF-beta 1 modulation of urokinase and PAI-1 expression in human bronchial epithelial cells.
- Author
-
Gerwin BI, Keski-Oja J, Seddon M, Lechner JF, and Harris CC
- Subjects
- Bronchi drug effects, Cells, Cultured, Epithelium drug effects, Epithelium metabolism, Fibroblasts drug effects, Fibroblasts metabolism, Humans, Kinetics, RNA, Messenger genetics, Bronchi metabolism, Gene Expression drug effects, Plasminogen Inactivators metabolism, Transforming Growth Factor beta pharmacology, Urokinase-Type Plasminogen Activator genetics
- Abstract
Normal human bronchial epithelial (NHBE) cells respond to signals initiated by the binding of transforming growth factor-beta type 1 (TGF-beta 1) to its surface receptors by activating pathways that result in terminal squamous differentiation. By use of both normal and SV40 T-antigen-immortalized cells, it was found that treatment with TGF-beta 1 transiently increases mRNA levels for urokinase (uPA) and plasminogen activator inhibitor type 1 (PAI-1) approximately 5- and 50-fold, respectively, within 4 h. In NHBE cells, PAI-1 protein is increased by TGF-beta 1 in both extracellular matrix and medium. The net effect of TGF-beta 1 on plasminogen activator activity in the medium was a 50% reduction as measured by a caseinolytic assay. A T-antigen-immortalized bronchial epithelial cell line that does not undergo squamous differentiation in response to TGF-beta 1 but binds this growth factor did not respond to TGF-beta 1 by modulation of either uPA or PAI-1 expression. Comparison of human bronchial epithelial, pleural mesothelial, and lung fibroblastic cell strains indicated that the epithelial cells have a constitutively higher ratio of uPA to PAI-1 mRNA expression. These data suggest that modulation of pericellular proteolysis in bronchial epithelial cells in response to TGF-beta 1 represents a significant biological change in their pericellular environment. The induction of uPA and PAI-1 expression in human bronchial epithelial cells may be related to the ability of the cell to undergo squamous differentiation in response to TGF-beta 1. These observations identify specific changes in gene expression that may serve as markers for the differentiation process.(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1990
- Full Text
- View/download PDF
43. Differential effects of cigarette smoke condensate and its fractions on cultured normal and malignant human bronchial epithelial cells.
- Author
-
Miyashita M, Willey JC, Sasajima K, Lechner JF, LaVoie EJ, Hoffmann D, Smith M, Trump BF, and Harris CC
- Subjects
- Bronchi cytology, Calcium metabolism, Cell Division, Cytosol metabolism, Epithelial Cells, Epithelium pathology, Humans, Ions, Osmolar Concentration, Phorbol 12,13-Dibutyrate metabolism, Reference Values, Tumor Cells, Cultured, Bronchi pathology, Carcinoma pathology, Lung Neoplasms pathology, Plants, Toxic, Smoke, Nicotiana
- Abstract
The differential effects of cigarette smoke condensate (CSC) and its fractions (neutral, basic, and acidic fractions) on proliferation and squamous differentiation of normal human bronchial epithelial (NHBE) cells versus human lung carcinoma cells were investigated. CSC, and the neutral and acidic fractions inhibited cellular proliferation more than the basic fraction. When compared to the acidic and basic fractions, CSC and the neural fraction were more effective in causing squamous differentiation of NHBE cells and inhibiting specific binding of phorbol dibutyrate (PDBU). There were no significant changes in ionized cytosolic calcium concentration when NHBE cells were treated with CSC. In contrast to the normal epithelial cells, neither HUT-292 nor the 3 other carcinoma cell lines examined showed marked squamous morphological changes when exposed to either CSC or its fractions and the carcinoma cells were more resistant to their inhibiting effects on cellular proliferation. These results are consistent with the hypothesis that differential effects of tobacco smoke components on cellular proliferation may allow clonal expansion of preneoplastic and neoplastic human bronchial epithelial cells during lung carcinogenesis.
- Published
- 1990
- Full Text
- View/download PDF
44. Clonal growth of epithelial cells from normal adult human bronchus.
- Author
-
Lechner JF, Haugen A, Autrup H, McClendon IA, Trump BF, and Harris CC
- Subjects
- Animals, Blood, Bronchi ultrastructure, Calcium pharmacology, Clone Cells, Cytological Techniques, Epithelial Cells, Growth Substances pharmacology, Humans, Mice, Microscopy, Electron, Scanning, Bronchi cytology
- Abstract
Normal primary epithelial cell cultures devoid of fibroblastic cells have been developed from tissue explants of adult human bronchi. Conditions for clonal growth of secondary cultures of bronchial epithelial cells were optimized by coculturing the human cells with mitomycin C growth-arrested Swiss 3T3 mouse feeder cells, lowering the calcium concentration of medium M199, and supplementing it with hydrocortisone, insulin, cholera toxin, epidermal growth factor, and 1.25% fetal bovine serum. The epithelial cells grew for an average of 35 population doublings and had the normal human karyotype, expressed keratin and blood group antigen epithelial cell markers, metabolized benzo(a)pyrene, and were capable of differentiating into both ciliated and squamous cells. This culture system makes it potentially possible to investigate various aspects of differentiation and carcinogenesis in human bronchial epithelial cells.
- Published
- 1981
45. Differential properties among clones of simian virus 40-transformed human epithelial cells.
- Author
-
Kaighn ME, Narayan KS, Ohnuki Y, Jones LW, and Lechner JF
- Subjects
- Agar, Blood Physiological Phenomena, Calcium pharmacology, Cell Division drug effects, Cell Size, Clone Cells drug effects, Clone Cells pathology, Clone Cells ultrastructure, Clone Cells virology, Culture Media, Epidermal Growth Factor pharmacology, Epithelial Cells drug effects, Epithelial Cells pathology, Epithelial Cells ultrastructure, Fibroblast Growth Factors pharmacology, Fibroblasts drug effects, Fibroblasts pathology, Fibroblasts ultrastructure, Fibroblasts virology, Growth Substances metabolism, Growth Substances pharmacology, Humans, Karyotyping, Magnesium pharmacology, Male, Microscopy, Electron, Ploidies, Prostate cytology, Antigens, Polyomavirus Transforming physiology, Cell Transformation, Viral, Epithelial Cells virology, Simian virus 40 physiology
- Abstract
Monolayer cultures of human prostatic epithelial cells were exposed to SV40 virus at 35th population doubling. Clones were isolated from infected plates after growth had ceased on the control plates. The nuclei of these clones were virtually all positive for viral T-antigen by immunofluorescence. When the properties of three of these lines were compared to those of normal cells, they were found to have altered morphology, ultrastructure, chromosomes, and growth behavior. All transformed lines had reduced serum dependence and were capable of growing in soft agar. However, their reduced serum dependence was not due to reduced growth factor requirements because each subline's response to growth factors was different.
- Published
- 1980
- Full Text
- View/download PDF
46. Asbestos-associated chromosomal changes in human mesothelial cells.
- Author
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Lechner JF, Tokiwa T, LaVeck M, Benedict WF, Banks-Schlegel S, Yeager H Jr, Banerjee A, and Harris CC
- Subjects
- Asbestos, Serpentine, Humans, Karyotyping, Lung Neoplasms genetics, Mesothelioma genetics, Microscopy, Electron, Scanning, Phagocytosis, Asbestos toxicity, Chromosomes, Human, Lung ultrastructure, Lung Neoplasms ultrastructure, Mesothelioma ultrastructure, Pleural Effusion
- Abstract
Replicative cultures of human pleural mesothelial cells were established from noncancerous adult donors. The cells exhibited normal mesothelial cell characteristics including keratin, hyaluronic acid mucin, and long branched microvilli, and they retained the normal human karyotype until senescence. The mesothelial cells were 10 and 100 times more sensitive to the cytotoxic effects of asbestos fibers than normal human bronchial epithelial or fibroblastic cells, respectively. In addition, cultures of mesothelial cells that survived two cytotoxic exposures of amosite fibers were aneuploid with consistent specific chromosomal losses indicative of clonal origin. These aneuploid cells exhibit both altered growth control properties and a population doubling potential of greater than 50 divisions beyond the culture life span (30 doublings) of the control cells.
- Published
- 1985
- Full Text
- View/download PDF
47. Differential effects of 12-O-tetradecanoylphorbol-13-acetate on cultured normal and neoplastic human bronchial epithelial cells.
- Author
-
Willey JC, Moser CE Jr, Lechner JF, and Harris CC
- Subjects
- Cell Division drug effects, Cell Line, Cell Survival drug effects, Cells, Cultured, Clone Cells, Epithelial Cells, Epithelium drug effects, Humans, Kinetics, Lung drug effects, Lung pathology, Lung Neoplasms pathology, Phorbols toxicity, Tetradecanoylphorbol Acetate toxicity
- Abstract
The effects of the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) on 10 human lung carcinoma cell lines were compared to those seen on normal human bronchial epithelial (NHBE) cells. TPA (0.1 to 100 nM) did not enhance the clonal growth rate for any of the cell lines. As little as 3 nM TPA induced the NHBE cells to undergo terminal squamous differentiation and thus completely inhibited their proliferation; in contrast, none of the carcinoma cell lines was significantly inhibited at this concentration, and they all continued to proliferate in as much as 100 nM TPA. To determine if this lack of TPA inhibition of clonal growth reflected resistance to TPA induction of terminal squamous differentiation, we measured the ability of TPA to induce cross-linked envelope formation and to increase plasminogen activator activity in four carcinoma cell lines. Cross-linked envelopes were not induced in two lines, and only a small number were induced in the other two lines relative to NHBE cells; plasminogen activator activity was induced in NHBE cells but not in any of the cell lines.
- Published
- 1984
48. Ion selective electrode for determination of chloride ion in biological materials, food products, soils and waste water.
- Author
-
Sekerka I and Lechner JF
- Subjects
- Animals, Beverages analysis, Cattle, Chlorides blood, Chlorides urine, Electrodes, Fruit analysis, Humans, Industrial Waste analysis, Meat Products analysis, Vegetables analysis, Chlorides analysis, Food Analysis, Soil analysis, Water analysis
- Abstract
The chloride ion selective electrode is used for a rapid, simple, and reliable determination of chloride ion in biological materials (blood serum, urine, fish, and plant tissues), food products (milk, beef extract, nutrient broth and orange, tomato, and grapefruit juices), soils, and waste water (industrial and municipal). The method consists of treating the samples with perchloric acid (pH 1) and potassium peroxydisulfate and determining the chloride content either by a calibration curve or by known addition or analyte addition, using the chloride ion selective electrode. Such sample treatment eliminates most of the interferences occurring in the samples, including iodide, complexing and reducing compounds, and macromolecular and surface-active species. The method is suitable for a wide range of chloride concentration, e.g., 5010 ppm Cl- in nutrient broth and 4890 ppm in beef extract and as low as 12 and 80 ppm in soil extracts.
- Published
- 1978
49. Replicative cultures of adult human and rhesus monkey liver epithelial cells.
- Author
-
Lechner JF, Cole KE, Reddel RR, Anderson L, and Harris CC
- Subjects
- Animals, Cell Differentiation, Cell Division, Cells, Cultured physiology, Culture Media, DNA genetics, Epithelial Cells, Humans, Macaca mulatta, Methods, Phenotype, Transfection, Liver cytology
- Abstract
Exploratory experiments indicate that media containing lipids, phosphoethanolamine, epidermal growth factor, insulin, cholera toxin, bovine pituitary extract, chemically denatured serum, and triiodothyronine will support replicative cultures of normal liver epithelial cells obtained from adult Rhesus monkey and human donors. In addition, we have extended the culture population doubling potential of the human liver epithelial cells by their transfection with a plasmid containing the SV40 virus T-antigen gene. The T-antigen gene-containing cells continued to express albumin through 40 population doublings. Finally, results of preliminary experiments suggest that it may be possible to induce human liver epithelial cells to undergo differentiation to hepatocyte-like cells either by injecting them into the spleen of an athymic nude mouse or by incorporating them into a collagen "tissue equivalent" matrix.
- Published
- 1989
50. Induction of squamous differentiation of normal human bronchial epithelial cells by small amounts of serum.
- Author
-
Lechner JF, Haugen A, McClendon IA, and Shamsuddin AM
- Subjects
- Blood Physiological Phenomena, Calcium pharmacology, Cholera Toxin pharmacology, Clone Cells cytology, Epithelial Cells, Humans, Microscopy, Electron, Tretinoin pharmacology, Bronchi cytology, Cell Differentiation drug effects, Culture Media
- Abstract
Recently we reported a low calcium (110 microM) serum-free medium (LHC-1) for clonal growth of normal human bronchial epithelial (NHBE) cells. NHBE cells within colonies are small (mean surface area = 1,250 mu2) rarely migratory, have few tonofilaments, and multiply with an average population doubling time of 28 h. We have also noted that adding small amounts of blood-derived serum to LHC-1 medium (as little as 2%) significantly decreased the clonal growth rate. We have now found that the growth inhibiting effect of serum is due to the induction of squamous (terminal) differentiation. Serum quickly increases the size of the cells (mean surface area = 4,900 mu2). In addition, the cells acquire numerous desmosomal junctions and an extensive network of keratin bundles. In contrast, human lung carcinoma cells multiply rapidly at clonal density in LHC-1 medium containing as much as 8% serum. Although high concentrations of calcium ions in the medium are known to induce squamous differentiation of epidermal keratinocytes in the absence of serum, high levels of Ca2+ (up to 1,000 microM) increased the number of desmosomal junctions, but did not significantly affect the clonal growth rate or size of the NHBE cells. However, high concentrations of calcium (above 450 microM) were found to potentiate serum differentiation-inducing activity. On the other hand, cholera toxin (10 ng/ml) inhibited the differentiation-inducing activity of serum. These results show that squamous differentiation of NHBE cells can be induced by serum and the potency of these serum factors can be modulated. In addition, the data show that lung carcinoma cells differ from their normal counterparts by not undergoing differentiation in the presence of serum.
- Published
- 1984
- Full Text
- View/download PDF
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