177 results on '"Princler GL"'
Search Results
102. Plasmacytomas and mesothelioma.
- Author
-
Perry, Michael C., Solinger, Alan, Farhangi, Mehdi, and Luger, Alan
- Published
- 1978
- Full Text
- View/download PDF
103. The biology of hairy cell leukemia.
- Author
-
NIELSEN, BENDT
- Published
- 1995
- Full Text
- View/download PDF
104. Demonstration and partial characterization of the interferon-gamma receptor on human B lymphocytes.
- Author
-
Nakagawa, Toshimasa, Nakagawa, Naoko, Delsing, Gita A., Volkman, David, and Kehrl, John H.
- Published
- 1989
- Full Text
- View/download PDF
105. Proliferation of human malignant astrocytomas is dependent on Ras activation.
- Author
-
Guha, Abhijit, Feldkamp, Matthias M, Lau, Nelson, Boss, Gerry, and Pawson, Anthony
- Subjects
CELL proliferation ,ASTROCYTOMAS ,MICROBIAL mutation ,MEDICAL genetics - Abstract
Overexpression and activation of receptor tyrosine kinases, such as platelet derived growth factor receptors (PDGFRs) and epidermal growth factor receptor (EGFR), leads to proliferation of human malignant astrocytoma cells. Although oncogenic mutations affecting Ras are not prevalent in human malignant astrocytomas, we have investigated whether levels of activated Ras.GTP might be elevated in these tumors secondary to the mitogenic signals originating from activated receptor tyrosine kinases. In support of this hypothesis high levels of Ras.GTP, similar to those found in oncogenic Ras transformed fibroblasts, were present in four established human malignant astrocytoma cell lines which express PDGFRs and EGFR, and 20 operative malignant astrocytoma specimens. Stimulation of PDGFR's and EGFR's induced tyrosine phosphorylation of the Shc adaptor protein and its association with Grb2, suggesting a mechanism by which Ras may be activated in human malignant astrocytoma cells. Furthermore, blocking Ras activation by expression of the Ha-Ras-Asn17 dominant-negative mutant, or by farnesyl transferase inhibitors, decreased in vitro proliferation of the human astrocytoma cell lines. These results support the hypothesis that proliferative signals from receptor tyrosine kinases expressed by human malignant astrocytoma cells utilize the Ras mitogenic pathway. Pharmacological inhibitors of the Ras pathway may therefore be of therapeutic value in these presently terminal tumors. [ABSTRACT FROM AUTHOR]
- Published
- 1997
- Full Text
- View/download PDF
106. Interferon therapy of non-Hodgkin's lymphoma.
- Author
-
Foon, Kenneth A., Roth, Mark S., and Bunn, Paul A.
- Published
- 1987
- Full Text
- View/download PDF
107. Clinical overview of alpha interferon. Studies and future directions.
- Author
-
Spiegel, Robert J.
- Published
- 1987
- Full Text
- View/download PDF
108. Alpha-fetoprotein production by hepatocellular carcinoma is prognostic of poor patients survival.
- Author
-
Izumi, Ryohei, Shimizu, Kohichi, Kiriyama, Masato, Hashimoto, Tetsuo, Urade, Masaaki, Yagi, Masato, Mizukami, Yuji, Nonomura, Akitaka, and Miyazaki, Itsuo
- Published
- 1992
- Full Text
- View/download PDF
109. Drug-Resistance Patterns Assessed From Tumor Marker Analysis.
- Author
-
Carl, Jesper
- Abstract
We analyzed the levels of the tumor markers alphafetoprotein and human chorionic gonadotropin during the course of treatment in 19 patients with nonseminomatous germ cell tumors. We calculated the fractional tumor kill at each cycle using assumptions of exponential tumor growth and exponential marker decay and assumptions assuring that marker production reflects the size of the clonogenic tumor. The observed pattern of decrease was compared with three theoretical models. The first (Skipper) assumes that sensitive and resistant populations are present at the beginning of treatment. The second (Goldie and Coldman) assumes an initially sensitive population with mutation causing subsequent treatment resistance. Both models, under a wide range of parameter values, predict a much more rapid decrease in fractional tumor kill per treatment cycle than was observed. A model in which there are four clones of differing sensitivity at the start of treatment was able to adequately describe the observed time course of tumor killing. [J Natl Cancer Inst 81:1631–1639, 1989] [ABSTRACT FROM PUBLISHER]
- Published
- 1989
110. Biologic Markers in Lung Cancer.
- Author
-
Vincent, Ronald G.
- Published
- 1982
- Full Text
- View/download PDF
111. Influence of methionine administration on serum alpha-fetoprotein levels in ethionine-injured rats.
- Author
-
Miyazaki, M., Watanabe, A., Wahid, S., Tsunashima, M., and Sato, J.
- Published
- 1982
- Full Text
- View/download PDF
112. Delayed cutaneous hypersensitivity reaction to crude and semi-purified tumor extracts in cancer patients.
- Author
-
Canevari, Silvana, Fossati, Giuseppe, Miotti, Silvia, Della Porta, Giuseppe, Grandi, Cesare, and Pizzocaro, Giorgio
- Abstract
A positive delayed cutaneous hypersensitivity reaction (DCHR) was observed to only one of five KCl soluble extracts from as many different tumoral kidneys in nine of 11 patients with kidney cancer. None of the autologous normal renal tissue extracts gave a positive reaction. SDS-PAGE analysis showed a predominant component with a molecular weight corresponding to that of serum albumin in all the four negative cancer extracts. Lipoproteins and serum albumin were removed by ultracentrifugal flotation on KBr and by affinity chromatography on antiserum albumin (α-HSA), respectively, from one of the negative crude extracts. KCl extract, F fraction of KBr, and unbound material from the α-HSA column were injected simultaneously into nine patients with renal cancer. Positive DCHRs were seen to the three extracts in no patients, in three, and in eight, respectively. The α-HSA unbound fraction was positive in three of 13 patients with tumor at a site other than the kidney. The same extraction procedure was applied to normal autologous kidney tissue, and positive reactivity was observed in one of eight and three of nine patients with kidney cancer to the F and α-HSA unbound fractions, respectively. An aliquot of KCl tumor extract was passed through the α-HSA column without the preliminary flotation on KBr, and the unbound fraction was positive in eight of nine patients with kidney cancer and in eight of twelve patients with other types of tumor. Three different melanomas were extracted in the same way and an increased percentage of DCHRs was found after removal of lipoproteins and HSA in melanoma patients. This reactivity, however, was not histologically related since patients with tumors other than melanoma reacted as well as melanoma patients. These data indicate that the removal of lipoproteins and HSA from crude tumor extracts may unmask or increase an existing antigenicity. The tumor-type-related experiments, however, suggest that these biochemical procedures are useful for kidney tumors but not for melanomas. [ABSTRACT FROM AUTHOR]
- Published
- 1981
- Full Text
- View/download PDF
113. Molecular lesions in cancer.
- Author
-
Busch, Harris
- Abstract
Newer methods of identifying biochemical events associated with cancer include recombinant DNA technology, monoclonal antibodies and improved analysis of nuclear and other cell functions to determine specific events which occur commonly in cancer cells. 'One-gene' products offer potential opportunities for new approaches to cancer treatment and the hope of inducing differentiation of cancer cells toward their normal counterparts. Studies on antigens which react with monoclonal antibodies offer the opportunity for 'Iepitope attack' which may be effected by improved drugs or by design of totally new drugs to bind to specific reactive sites. The complexity and pleiomorphism of cancer do not permit predictions as to whether these approaches will be more effective than the empirical approach to cancer treatment. [ABSTRACT FROM AUTHOR]
- Published
- 1984
- Full Text
- View/download PDF
114. Cytokines as Therapeutic and Diagnostic Agents.
- Author
-
Elsässer-Beile, U. and von Kleist, S.
- Abstract
Cytokines are key mediators of immunity and inflammation. These proteins or glycoproteins act as communication signals between different populations of leukocytes but neither their effects nor their production are restricted to immune cells. In the last few years many new cytokines and their effects have been discovered and it was agreed that when the amino acid sequence of a new cytokine was established it would be assigned the name interleukin (IL), with an added number. The detection of cytokines in disease states promises to provide useful information for diagnostic purposes. The therapeutic utility of cytokines has been explored in many clinical and preclinical studies and in a wide variety of infectious diseases, autoimmune diseases and neoplasias. Since the production of cytokines is modulated by several biological agents such as hormones, prostaglandins and drugs, these may also serve as therapeutic targets for immunomodulation. Copyright © 1993 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]
- Published
- 1993
- Full Text
- View/download PDF
115. Prolactin receptor signal transduction in cells of the immune system.
- Author
-
Clevenger, C. V., Freier, D. O., and Kline, J. B.
- Published
- 1998
116. Association of Testicular Non-Hodgkin's Lymphomas with Elevated Serum Levels of Human Chorionic Gonadotropin-Like Material.
- Author
-
Møller, Michael B.
- Published
- 1996
- Full Text
- View/download PDF
117. Current treatment of hairy cell leukaemia.
- Author
-
Dearden, Claire and Catovsky, Daniel
- Published
- 1988
- Full Text
- View/download PDF
118. Serum Levels of Soluble IL-6 Receptor in Multiple Myeloma as Indicator of Disease Activity.
- Author
-
Papadaki, Helen, Kyriakou, Despina, Foudoulakis, Andreas, Markidou, Fotini, Alexandrakis, Michael, and Eliopoulos, George D.
- Published
- 1997
- Full Text
- View/download PDF
119. The assembly of triacylglycerol-rich lipoproteins: an essential role for the microsomal triacylglycerol transfer protein.
- Author
-
White, David A., Bennett, Andrew J., Billett, Michael A., and Salter, Andrew M.
- Abstract
Raised plasma triacylglycerol is an independent risk factor for cardiovascular disease, and an understanding of factors which regulate the synthesis and degradation of lipoproteins which carry triacylglycerol in the blood may lead to novel approaches to the treatment of hypertriacylglycerolaemia. An active microsomal triacylglycerol transfer protein (MTP) is essential for the assembly of particles which transport triacylglycerol through the circulation. After absorption in the intestine, dietary fat and fat-soluble vitamins are incorporated into chylomicrons in the intestinal epithelial cells, and these lipoproteins reach the bloodstream via the lymphatic system. Patients with the rare genetic disorder, abetalipoproteinaemia, in which MTP activity is absent, present clinically with fat-soluble vitamin and essential fatty acid deficiency, indicating a key role for MTP in the movement of fat into the body. The triacylglycerol-rich lipoprotein found in fasting blood, VLDL, is assembled in the liver by an MTP-dependent process similar to chylomicron assembly, and transports triacylglycerol to extra-hepatic tissues such as adipose tissue and heart. In the absence of MTP activity, VLDL are not synthesized and only extremely low levels of triacylglycerol are present in the blood. Dietary components, including fat, cholesterol and ethanol, can modify the expression of the MTP gene and, hence, MTP activity. The present review summarizes current knowledge of the role of MTP in the assembly and secretion of triacylglycerol-rich lipoproteins, and the regulation of its activity in both animal and cell systems. [ABSTRACT FROM PUBLISHER]
- Published
- 1998
- Full Text
- View/download PDF
120. Silencers of HTLV-1 and HTLV-2: the pX-encoded latency-maintenance factors.
- Author
-
Harrod, Robert
- Subjects
HTLV ,ADULT T-cell leukemia ,IMMOBILIZED proteins ,GENE silencing ,GENE expression ,MITOSIS ,GOLGI apparatus - Abstract
Of the members of the primate T cell lymphotropic virus (PTLV) family, only the human T-cell leukemia virus type-1 (HTLV-1) causes disease in humans—as the etiological agent of adult T-cell leukemia/lymphoma (ATLL), HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP), and other auto-inflammatory disorders. Despite having significant genomic organizational and structural similarities, the closely related human T-cell lymphotropic virus type-2 (HTLV-2) is considered apathogenic and has been linked with benign lymphoproliferation and mild neurological symptoms in certain infected patients. The silencing of proviral gene expression and maintenance of latency are central for the establishment of persistent infections in vivo. The conserved pX sequences of HTLV-1 and HTLV-2 encode several ancillary factors which have been shown to negatively regulate proviral gene expression, while simultaneously activating host cellular proliferative and pro-survival pathways. In particular, the ORF-II proteins, HTLV-1 p30
II and HTLV-2 p28II , suppress Tax-dependent transactivation from the viral promoter—whereas p30II also inhibits PU.1-mediated inflammatory-signaling, differentially augments the expression of p53-regulated metabolic/pro-survival genes, and induces lymphoproliferation which could promote mitotic proviral replication. The ubiquitinated form of the HTLV-1 p13II protein localizes to nuclear speckles and interferes with recruitment of the p300 coactivator by the viral transactivator Tax. Further, the antisense-encoded HTLV-1 HBZ and HTLV-2 APH-2 proteins and mRNAs negatively regulate Tax-dependent proviral gene expression and activate inflammatory signaling associated with enhanced T-cell lymphoproliferation. This review will summarize our current understanding of the pX latency-maintenance factors of HTLV-1 and HTLV-2 and discuss how these products may contribute to the differences in pathogenicity between the human PTLVs. [ABSTRACT FROM AUTHOR]- Published
- 2019
- Full Text
- View/download PDF
121. Natural killer cell cytolytic activity is necessary for in vivo antitumor activity of the dipeptide L-glutamyl-L-tryptophan.
- Author
-
Smith DL, Cai J, Zhu S, Wei W, Fukumoto J, Sharma S, Masood R, and Gill PS
- Subjects
- Animals, Cell Division drug effects, Cytoplasmic Granules metabolism, Cytotoxicity, Immunologic, Flow Cytometry, Humans, Interferon-gamma deficiency, Interferon-gamma genetics, Interferon-gamma metabolism, Interleukin-12 deficiency, Interleukin-12 genetics, Interleukin-12 metabolism, Lung Neoplasms immunology, Lung Neoplasms secondary, Melanoma immunology, Melanoma secondary, Membrane Glycoproteins metabolism, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Neoplasms, Experimental, Perforin, Pore Forming Cytotoxic Proteins, T-Lymphocytes physiology, Tumor Cells, Cultured, Angiogenesis Inhibitors therapeutic use, Dipeptides therapeutic use, Killer Cells, Natural physiology, Lung Neoplasms drug therapy, Melanoma drug therapy
- Abstract
A dipeptide, L-glutamyl L-tryptophan (L-glu-L-trp), was identified in a screen for immunomodulators in the soluble fraction of the thymus. L-glu-L-trp inhibits tumor growth in mice without showing direct cellular toxicity in a variety of human tumor cell lines. L-glu-L-trp antitumor activity in vivo requires the presence of natural killer (NK) cells. Defective trafficking of cytoplasmic granules caused by the Lyst mutation also resulted in loss of antitumor activity of the dipeptide. The effect of L-glu-L-trp on tumor growth in mice with targeted gene mutations demonstrated the absolute requirement for perforin for antitumor activity. The requirement of 2 major modulators of NK cell activity, gamma interferon (IFNgamma) and interleukin (IL)-12, were also tested. L-glu-L-trp had full antitumor activity in IFNgamma knockout mice, but had significantly diminished activity in IL-12 knockout mice. These data show that L-glu-L-trp antitumor activity in mice is dependent on cytolytic cell activity of NK or NKT cells. L-glu-L-trp in vivo regulates NK cell function independent of IFNgamma but partly dependent on IL-12., (Copyright 2003 Wiley-Liss, Inc.)
- Published
- 2003
- Full Text
- View/download PDF
122. Hairy-cells are not lysed by NK-cells.
- Author
-
Sigaux, F., Chapuis, F., Castaigne, S., Degos, L., Flandrin, G., and Gluckman, J.
- Published
- 1987
- Full Text
- View/download PDF
123. Proteomic and Metabolomic Approaches to Biomarker Discovery
- Author
-
Haleem J. Issaq, Timothy D. Veenstra, Haleem J. Issaq, and Timothy D. Veenstra
- Subjects
- Metabolism--Regulation, Proteomics--Methodology, Biochemical markers
- Abstract
Proteomic and Metabolomic Approaches to Biomarker Discovery, Second Edition covers techniques from both proteomics and metabolomics and includes all steps involved in biomarker discovery, from study design to study execution. The book describes methods and presents a standard operating procedure for sample selection, preparation and storage, as well as data analysis and modeling. This new standard effectively eliminates the differing methodologies used in studies and creates a unified approach. Readers will learn the advantages and disadvantages of the various techniques discussed, as well as potential difficulties inherent to all steps in the biomarker discovery process. This second edition has been fully updated and revised to address recent advances in MS and NMR instrumentation, high-field NMR, proteomics and metabolomics for biomarker validation, clinical assays of biomarkers and clinical MS and NMR, identifying microRNAs and autoantibodies as biomarkers, MRM-MS assay development, top-down MS, glycosylation-based serum biomarkers, cell surface proteins in biomarker discovery, lipodomics for cancer biomarker discovery, and strategies to design studies to identify predictive biomarkers in cancer research. - Addresses the full range of proteomic and metabolomic methods and technologies used for biomarker discovery and validation - Covers all steps involved in biomarker discovery, from study design to study execution - Serves as a vital resource for biochemists, biologists, analytical chemists, bioanalytical chemists, clinical and medical technicians, researchers in pharmaceuticals and graduate students
- Published
- 2020
124. Neurosurgical Review : For Daily Clinical Use and Oral Board Preparation
- Author
-
Vasilios A. Zerris and Vasilios A. Zerris
- Subjects
- Study Guide, Neurosurgical Procedures--methods
- Abstract
Robust ABNS exam prep and didactic review of the entire spectrum of neurosurgery from A to ZThe American Board of Neurological Surgery oral examination has undergone periodic review and revision over the years, with a new format instituted in spring 2017. This review book is specifically geared to the new format. The ABNS oral examination process is relevant, rigorous, and of value to the neurosurgical specialty and the public, ensuring neurosurgeons meet the highest standards of practice.Neurosurgical Review: For Daily Clinical Use and Oral Board Preparation by Vasilios A. Zerris and distinguished contributors is a multimodal and a visually rich prep tool for the ABNS exam. The resource provides a unique approach to studying and melding online didactic materials with audio-enhanced charts. Readers can use the material as a complete online exam prep course with audio, or use the print version as a quick reference guide.Key FeaturesCharts and schematics provide an excellent learning tool and study prepThe high yield and easy to memorize format helps readers'visualize'knowledgeAudio files enhance the ability to create a mental framework, thereby increasing comprehension and retention of contentCases presented at the end of each chapter focus primarily on core material tested in the general neurosurgery ABNS exam session taken by all candidates irrespective of their declared subspecialtyThis is an essential textbook for neurosurgical residents, fellows, and practitioners prepping for the ABNS boards. It also serves as a user-friendly refresher of fundamental knowledge all neurosurgeons need to know.
- Published
- 2019
125. Principles of Cancer Biotherapy
- Author
-
Robert K. Oldham, Robert O. Dillman, Robert K. Oldham, and Robert O. Dillman
- Subjects
- Oncology, Immunology, Biochemistry, Radiology, Bioethics
- Abstract
At the time of the first edition of Principles of Cancer Biotherapy in 1987, this book represented the first comprehensive textbook on biological therapy. In 1991, when the second edition was published, there was still some doubt on the part of many oncologists and cancer researchers as to the therapeutic value of these new approaches. By 2003 and the fourth edition, it was generally agreed that biopharmaceuticals were producing major opportunities for new cancer therapies. Cancer biotherapy has now truly matured into the fourth modality of cancer treatment. This fifth revised edition describes the tremendous progress that has been made in recent years using biologicals in cancer treatment. This book summarizes an evolving science and a rapidly changing medical practice in biotherapy. In this new millennium, it is now possible to envision a much more diversified system of cancer research and treatment that will afford greater opportunities for a patient's personalized cancer treatment. This was first envisioned in the 1987 initial edition of this textbook and is now a'new'and popular approach to cancer treatment. Some forms of cancer biotherapy use the strategy of tumor stabilization and control though continued biological therapy, akin to the use of insulin in the treatment of diabetes. This textbook illustrates new methods of thinking and new strategies for control of cancer. It is always difficult to move from past dogma to future opportunity, but this fifth edition of Principles of Cancer Biotherapy illustrates why it is so important to the patients for researchers and clinicians to explore and quickly apply these new opportunities in cancer biotherapy.
- Published
- 2019
126. MEF2D sustains activation of effector [Foxp3.sup.+] Tregs during transplant survival and anticancer immunity
- Author
-
Giorgio, Eros Di, Wang, Liqing, Xiong, Yan, Akimova, Tatiana, Christensen, Lanette M., Han, Rongxiang, Samanta, Arabinda, Trevisanut, Matteo, Bhatti, Tricia R., Beier, Ulf H., and Hancock, Wayne W.
- Subjects
Cancer treatment -- Research ,Cancer research ,Transcription factors -- Health aspects ,Genetic regulation -- Health aspects ,T cells -- Genetic aspects -- Health aspects ,Health care industry - Abstract
The transcription factor MEF2D is important in the regulation of differentiation and adaptive responses in many cell types. We found that among T cells, MEF2D gained new functions in [Foxp3.sup.+] T regulatory (Treg) cells due to its interactions with the transcription factor Foxp3 and its release from canonical partners, like histone/protein deacetylases. Though not necessary for the generation and maintenance of Tregs, MEF2D was required for the expression of IL-10, CTLA4, and Icos, and for the acquisition of an effector Treg phenotype. At these loci, MEF2D acted both synergistically and additively to Foxp3, and downstream of Blimp1. Mice with the conditional deletion in Tregs of the gene encoding MEF2D were unable to maintain long-term allograft survival despite costimulation blockade, had enhanced antitumor immunity in syngeneic models, but displayed only minor evidence of autoimmunity when maintained under normal conditions. The role played by MEF2D in sustaining effector [Foxp3.sup.+] Treg functions without abrogating their basal actions suggests its suitability for drug discovery efforts in cancer therapy., Introduction The roles played by T regulatory (Treg) cells in the maintenance of immune homeostasis are well established (1). By restricting T cell functions, Tregs restrain the onset of autoimmunity [...]
- Published
- 2020
- Full Text
- View/download PDF
127. Casarett & Doull's Toxicology: The Basic Science of Poisons, 9th Edition
- Author
-
Curtis D. Klaassen and Curtis D. Klaassen
- Abstract
Publisher's Note: Products purchased from Third Party sellers are not guaranteed by the publisher for quality, authenticity, or access to any online entitlements included with the product. Toxicology's gold-standard text - completely updated to reflect the latest breakthroughs and discoveries A Doody's Core Title for 2019! Casarett & Doull's Toxicology: The Basic Science of Poisons, Ninth Edition equips you with an unsurpassed understanding of modern toxicology, including the key principles, concepts, mechanisms, chemical-specific toxicity, and modes of thought that are the foundation of the discipline. This trusted classic not only delivers a comprehensive review of the essential components of toxicology, it offers the most up-to-date, revealing, and in-depth look at the systemic responses of toxic substance available anywhere. Casarett & Doull's Toxicology: The Basic Science of Poisons, Ninth Edition is logically divided into seven sections: •General Principles of Toxicology •Disposition of Toxicants •Non-Organ Directed Toxicity •Target Organ Toxicity •Toxic Agents •Environmental Toxicology •Applications of Toxicology Many new contributors capture the progress made in toxicology over the past few years: This edition is markedly updated from the previous edition, with more than one-third of the chapters authored by scientists who have not made previous contributions to the book. Sharing their expertise, they deliver dynamic new coverage of the importance of apoptosis, autophagy, cytokines, growth factors, oncogenes, cell cycling, receptors, gene regulation, protective mechanisms, repair mechanisms, transcription factors, signaling pathways, transgenic mice, knock-out mice, humanized mice, polymorphisms, microarray technology, second-generation sequencing, genomics, proteomics, epigenetics, exposome, microbiota, read across, adverse outcome pathways, high-content screening, computational toxicology, innovative test methods, and organ-on-a-chip in understanding the mechanisms of toxicity and the regulation of chemicals. A true “essential” If you are in need of an up-to-date, all-in-one overview of the biomedical and environmental aspects of toxicology - written by experts, and presented in full color, your search ends here.
- Published
- 2018
128. Infectious Agents Associated Cancers: Epidemiology and Molecular Biology
- Author
-
Qiliang Cai, Zhenghong Yuan, Ke Lan, Qiliang Cai, Zhenghong Yuan, and Ke Lan
- Subjects
- Microbial carcinogenesis
- Abstract
This book offers a state-of-the-art report on recent discoveries concerning viral, bacterial, and parasite infectious cancers. Cancer is one of the most common causes of death and diseases in human populations, and 15%-25% of human cancers in worldwide are considered to result from chronic infection by pathogens. Most oncology textbooks address genetic mutation, but not infectious agents such as viruses, bacteria and parasites. As such this book stimulates further research in the new area between cancers and chronic infection, and discusses the epidemiology and molecular biology of infectious causes of cancers. It also explores the prevention and treatment of infection-related cancers, and brings pathogenic research to the forefront in the never-ending endeavor to understand how pathogens maneuver and negotiate in a complex environment, including the micro/macro- environment of the human host. Further, it highlights the urgent need for a concerted program to develop vaccines and other diagnosis and interventions that will eventually help prevent and treat infectious cancers, and decrease their burden on human populations. It offers graduate students and researchers a comprehensive overview of the infectious causes of cancers.
- Published
- 2017
129. Chirurgische Onkologie : Histologie- und stadiengerechte Therapie maligner Tumoren
- Author
-
Franz P. Gall, Paul Hermanek, Jürgen Tonak, Franz P. Gall, Paul Hermanek, and Jürgen Tonak
- Subjects
- Surgery, Oncology
- Published
- 2013
130. Interferone : Präklinische und klinische Befunde
- Author
-
Norbert Niederle, Peter v. Wussow, Norbert Niederle, and Peter v. Wussow
- Subjects
- Oncology, Allergy, Immunology
- Abstract
Im ersten Teil des Buches werden Entwicklung, Aufbau und Systematik der Interferone sowie ihre Stellung innerhalb des Zytokin-Netzwerkes dargestellt. Weiterhin werden durch Interferone stimulierbare zytoplasmatische und nukleäre Veränderungen beschrieben. Der zweite Teil beschäftigt sich mit der klinischen Anwendung von Interferonen. Bei den wichtigsten malignen und benignen Krankheitsbildern werden die bisherigen Ergebnisse der Interferongabe dargestellt - auch in Kombination mit anderen systemischen und lokalen Behandlungsmaßnahmen - und mit herkömmlichen Behandlungsmethoden verglichen. Ziel des vorliegenden Buches ist es, möglichst umfassend und klar über Aufbau und Systematik des Interferonsystems sowie über seine bisherige klinische Bedeutung zu informieren.
- Published
- 2013
131. Proteomic and Metabolomic Approaches to Biomarker Discovery
- Author
-
Haleem J. Issaq and Haleem J. Issaq
- Subjects
- Biochemical markers, Proteomics
- Abstract
Proteomic and Metabolomic Approaches to Biomarker Discovery demonstrates how to leverage biomarkers to improve accuracy and reduce errors in research. Disease biomarker discovery is one of the most vibrant and important areas of research today, as the identification of reliable biomarkers has an enormous impact on disease diagnosis, selection of treatment regimens, and therapeutic monitoring. Various techniques are used in the biomarker discovery process, including techniques used in proteomics, the study of the proteins that make up an organism, and metabolomics, the study of chemical fingerprints created from cellular processes. Proteomic and Metabolomic Approaches to Biomarker Discovery is the only publication that covers techniques from both proteomics and metabolomics and includes all steps involved in biomarker discovery, from study design to study execution. The book describes methods, and presents a standard operating procedure for sample selection, preparation, and storage, as well as data analysis and modeling. This new standard effectively eliminates the differing methodologies used in studies and creates a unified approach. Readers will learn the advantages and disadvantages of the various techniques discussed, as well as potential difficulties inherent to all steps in the biomarker discovery process. A vital resource for biochemists, biologists, analytical chemists, bioanalytical chemists, clinical and medical technicians, researchers in pharmaceuticals, and graduate students, Proteomic and Metabolomic Approaches to Biomarker Discovery provides the information needed to reduce clinical error in the execution of research. - Describes the use of biomarkers to reduce clinical errors in research - Includes techniques from a range of biomarker discoveries - Covers all steps involved in biomarker discovery, from study design to study execution
- Published
- 2013
132. Diagnostik und Therapie von Hodentumoren
- Author
-
Hans-Joachim Schmoll, Lothar Weißbach, Hans-Joachim Schmoll, and Lothar Weißbach
- Subjects
- Oncology, Urology, Radiology, Surgery
- Published
- 2013
133. Therapy of Renal Diseases and Related Disorders
- Author
-
Wadi N. Suki, Shaul G. Massry, Wadi N. Suki, and Shaul G. Massry
- Subjects
- Kidneys--Diseases--Treatment, Urinary organs--Diseases--Treatment, Kidney Diseases--therapy
- Abstract
'Where are all these kidney patients coming from? A few perfection the study of the urinary sediment, clinically years ago we had never heard of kidney disease and now practical kidney function tests, and the natural history of a number of kidney diseases including glomerulonephritis. you are speaking of patients in the hundreds of thousands and indeed potentially millions.'My reply, not meant to William Goldring, Herbert Chasis, Dana Atchley, and others studied the effects of hypertension, endocarditis, be grim, was'From the cemetery, Sir.'This is a summary and circulatory diseases on the kidney and spawned suc of some Congressional testimony lance gave on behalf of extending kidney disease under Medicare. Where indeed cessive generations of alert clinical investigators, who be gan to chronicle the natural histories of a wide variety of were all the patients with kidney disease in the United States before World War II? They were certainly not kidney diseases. Quantitative studies of renal function flourished under a school headed by Homer Smith, and under the care of nephrologists! Nephrology was not listed in the questionnaires for any state or the American Medi surprisingly precise techniques were developed for study ing a whole range of explicit nephron functions. Imagine cal Association as a subspecialty or even as a special the joy with the advent of vascular catheterization to be interest.
- Published
- 2012
134. Epidemiology and Biology of Multiple Myeloma
- Author
-
G. Iris Obrams, Michael Potter, G. Iris Obrams, and Michael Potter
- Subjects
- Multiple myeloma--Epidemiology--Congresses, Multiple myeloma--Pathophysiology--Congresses, Blacks--congresses, Monoclonal Gammopathies, Benign--congresses, Multiple Myeloma--congresses, Risk Factors--congresses, Whites--congresses
- Abstract
On March 27, 1990, the National Cancer Institute sponsored a workshop on the epidemiology of multiple myeloma, held at the National Institutes of Health. This book comprises articles prepared by participants in this work shop. Discussed in these papers are: the descriptive and analytic epidemi ology, differences in risk factors between blacks and whites, monoclonal gammopathies and their progression, and hypotheses regarding the etiology and pathogenesis of multiple myeloma. Several epidemiologic research areas received particular attention during this workshop, and are reviewed in detail in this volume. There have been striking increases in the incidence of multiple myeloma over the past thirty years, especially among older individuals and blacks, which may not be entirely explained by changes in diagnostic capabilities. Occupational and environmental exposures have been associated with an increased risk of multiple myeloma, including farming exposures, occupational exposure to petroleum and rubber processing, exposure to ionizing radiation, and asso ciations with persistent virus infections. The most striking epidemiological finding is reflected in the differences in incidence rates of multiple myeloma which are twice as high in blacks as compared with whites. Further, since 1950 the mortality rates for multiple myeloma have quadrupled in blacks while doubling for whites. Among hematopoietic malignancies, multiple myeloma is the only one with increased incidence and mortality rates among blacks. 1\vo major possibilities for explaining ethnic/racial differences in suscepti bility to multiple myeloma are genetic and environmental factors.
- Published
- 2012
135. Cancer Management in Man : Detection, Diagnosis, Surgery, Radiology, Chronobiology, Endocrine Therapy
- Author
-
Alfred L. Goldson and Alfred L. Goldson
- Subjects
- Cancer--Treatment, Cancer--Diagnosis, Neoplasms--diagnosis, Neoplasms--therapy
- Abstract
Previous volumes in this series have discussed the current progression have identified a variety of targets and strategies state of our knowledge concerning the pathophysiology of to allow these goals to be realized. This volume critically cancer growth and progression. The complexity of the in reviews approaches towards cancer management in man at teraction of malignant neoplasms and the host, the the levels of: detection, diagnosis, surgery, radiology, heterogeneity of malignant cell subpopulations, and the chronobiology and endocrine treatment. existence of metastatic tumor cells resistant to drug thera Several chapters review selected methods of cancer diag pies remain as significant clinical challenges to clinical on nosis. In addition, a variety of on-going and novel ap cologists. Indeed, conventional treatment regimens of che proaches for cancer treatment are also presented in this volume. Progress in the early detection of malignant neo motherapy, surgery and radiology are often ineffective for the therapy of a large variety of established metastatic can plasms, coupled with novel approaches for the therapy of cer in patients. When one considers the insidiousness of such neoplasms, may ultimately yield safe and well-tolerated agents for the selective therapy of solid malignancies. New progressive neoplastic growth and the emergence of con tinuously more aggressive and malignant cellular subpop therapeutic approaches, directed towards the biochemical ulations one is overwhelmed with the challenges inherent in and molecular targets identified in the earlier volumes of this series, may ultimately lead to the generation of new mo attempting to control malignant neoplasms.
- Published
- 2012
136. Immunologic Approaches to the Classification and Management of Lymphomas and Leukemias
- Author
-
John M. Bennett, Kenneth A. Foon, John M. Bennett, and Kenneth A. Foon
- Subjects
- Lymphomas--Immunological aspects, Leukemia--Immunological aspects, Lymphomas--Classification, Leukemia--Classification, Lymphomas--Immunodiagnosis, Monoclonal antibodies--Therapeutic use, Leukemia--therapy, Lymphoma--classification, Lymphoma--therapy
- Abstract
Where do you begin to look for a recent, authoritative article on the diagnosis or management of a particular malignancy? The few general on cology textbooks are generally out of date. Single papers in specialized journals are informative but seldom comprehensive; these are more often preliminary reports on a very limited number of patients. Certain general journals frequently publish good indepth reviews of cancer topics, and published symposium lectures are often the best overviews available. Un fortunately, these reviews and supplements appear sporadically, and the reader can never be sure when a topic of special interest will be covered. Cancer Treatment and Research is a series of authoritative volumes which aim to meet this need. It is an attempt to establish a critical mass of oncology literature covering virtually all oncology topics, revised frequently to keep the coverage up to date, easily available on a single library shelf or by a single personal subscription. We have approached the problem in the following fashion. First, by dividing the oncology literature into specific subdivisions such as lung cancer, genitourinary cancer, pediatric oncology, etc. Second, by asking eminent authorities in each of these areas to edit a volume on the specific topic on an annual or biannual basis. Each topic and tumor type is covered in a volume appearing frequently and predictably, discussing current diagnosis, staging, markers, all forms of treatment modalities, basic biology, and more.
- Published
- 2012
137. Principles of Cancer Biotherapy
- Author
-
R.K. Oldham and R.K. Oldham
- Subjects
- Oncology, Cancer
- Abstract
At the time of the first edition of Principles of Cancer Biotherapy, this book represented the first comprehensive textbook on biological therapy. Whereas in 1991, when the second edition was published, there was still some doubt on the part of many oncologists and cancer researchers as to the therapeutic value of these new approaches, it is now generally agreed that biopharmaceuticals are producing major opportunities for new cancer therapies. Cancer biotherapy has truly matured into the fourth modality of cancer treatment. The third edition is now needed as a result of the tremendous progress that has been made in recent years using biologicals in cancer treatment. The book summarizes an evolving science and a rapidly changing medical practice. As we near the millennium, it now becomes possible to envision a much more diversified system of cancer research and treatment that will afford greater opportunities for patients. Some forms of cancer biotherapy use the strategy of tumour stabilization and control through continued biological therapy, akin to the use of insulin in the treatment of diabetes. This textbook illustrates new methods of thinking and new strategies for control of cancer. It is always difficult to move from past dogma to future opportunity, but this third edition of Principles of Cancer Biotherapy illustrates why it is so important to the patients, for researchers and clinicians to explore and apply these new opportunities in cancer biotherapy.
- Published
- 2012
138. Lung Cancer: Basic and Clinical Aspects : Basic and Clinical Aspects
- Author
-
Heine H. Hansen and Heine H. Hansen
- Subjects
- Lungs--Cancer--Diagnosis, Lungs--Cancer, Lung Neoplasms--diagnosis, Lung Neoplasms--therapy
- Abstract
Lung cancer is one of the biggest challenges in oncology today. The challenge is due to the recognition of the possibility of prevention in at least 70-80% of all the cases and the extreme difficulties encountered in the treatment of this neoplasm. Despite the knowledge of prevention measures such as cessation of cigarette smoking the incidence continues to increase in many countries. The increase is particularly notable in females in the west ernized countries where the death rate in females in certain regions sur passes that of breast cancer. Furthermore, in many developing countries lung cancer is now being diagnosed with increasing frequency in both sexes and it is expected to be a major cause of death in those countries later in this century or the beginning of next century if the tobacco consumption will continue its rapid rise. With respect to therapy the 1970'es brought considerable progress in understanding of the clinical behaviour of lung cancer thereby establishing the importance of distinguishing between the major histologic types. Thera peutic advancement was particularly experienced in small cell carcinoma with the introduction of combination chemotherapy after this special dis ease entity among lung cancers was recognized as being a disseminated dis ease in almost all cases at the time of diagnosis. It was expected that the improvement in therapy would have continued in the early 1980'es, not only for small cell lung cancer but also for the other cell types.
- Published
- 2012
139. Assessment of Tumour Response
- Author
-
B.W. Hancock and B.W. Hancock
- Subjects
- Tumors--Treatment--Evaluation, Neoplasm staging--Methods, Neoplasms--Therapy
- Abstract
The assessment of tumour response after treatment is one of the most important challenges in Oncology and the picture is so often complicated by the effects of therapy itself. Clinical assessment is still by far the most important method of assessment at our disposal but there is increasing dependence on investigations of all types as indices of response. This depen dence may be misplaced if inappropriate investigations are pursued and we have tried to emphasise in this book the importance of selectivity. Some indices of assessment (e. g. tumour markers, organ imaging) have a vital role to play; others (e. g. histopathology, genetics) are assuming greater impor tance as tumour behaviour becomes better understood. One subject, Immu nology, is still in its infancy as regards tumour follow-up, but shows much promise so that a full account of tumour immunology and trends in immu notherapy has been included. I am grateful to Dr. Brian Ross for his help with the chapter on Organ Imaging, to the Department of Medical Illustration for their ever-ready co-operation with illustrations and photographs and to Miss Shirley Francis for doing much of the typing. B. W. HANCOCK List of Contributors HANCOCK, B. W., MD, DCH, MRCP, Senior Lecturer in Medicine, Hon orary Consultant Physician, Royal Hallamshire & Weston Park Hospitals, Sheffield, U. K. NEAL, F. E., KSG, MBChB, FRCR, DMRT, Consultant Radiotherapist & Oncologist, Weston Park Hospital, Sheffield, u. K. POTTER, AM.
- Published
- 2012
140. Clinical Evaluation of Antitumor Therapy
- Author
-
Franco M. Muggia, Marcel Rozencweig, Franco M. Muggia, and Marcel Rozencweig
- Subjects
- Antineoplastic agents--Testing, Cancer--Chemotherapy, Clinical trials, Antineoplastic Agents--therapeutic use, Clinical Trials--methods, Neoplasms--drug therapy
- Abstract
The methodology of drug development has been the subject of extensive dis cussion by a relatively small group of individuals in industry and government who have been intimately concerned with the identification and study of new anticancer drugs. The Chemotherapy Program of the National Cancer In stitute has represented the major focus of initial efforts in drug development, as summarized in the historical perspective presented in chapter 1 and its references. It is no coincidence that the Chemotherapy Program was the origin of the Division of Cancer Treatment, a government entity that has had a pivotal role in the growth of clinical oncology. In an analogous fashion this book presents the methodology employed in the clinical study of anticancer drugs within the broad context of cancer treatment. The research orientation promulgated in the study of new drugs is a central theme in most oncolo gists'approach to the clinical problem of cancer. Therefore, we hope that this book will introduce readers to treatment research in clinical oncology. For the oncologist, the clinical evaluation of antitumor therapy is both part of the day-to-day management of specific patients and the critical considera tion of developing therapeutic alternatives. For physicians in other fields of medicine it is important to acquaint themselves with the basic tools of the oncologist. For people without medical training, including patients who might be interested in treatment research, many of the chapters may be overly technical.
- Published
- 2012
141. Biological Response Modifiers — Interferons, Double-Stranded RNA and 2′,5′-Oligoadenylates
- Author
-
W.E.G. Müller, H.C. Schröder, W.E.G. Müller, and H.C. Schröder
- Subjects
- Cytology, Cancer, Immunology, Biochemistry, Pharmacology, Allergy
- Abstract
Biological response modifiers are increasingly used in viral and cancer therapy. Since alterations of the immune system are the primary symptoms of HIV infection, especially therapies directed towards the modulation of the immune response have been under intense evaluation. This volume summarizes current knowledge of the interferon-based natural antiviral protection system including 2',5'-oligoadenylate and double-stranded RNA. It will also help to develop further a solid scientific rationale for the practical use of heterologous immunomodulators in the clinics.
- Published
- 2012
142. Gastrointestinal Cancer : Radiation Therapy
- Author
-
Ralph R., Jr. Dobelbower and Ralph R., Jr. Dobelbower
- Subjects
- Digestive organs--Cancer, Digestive organs--Cancer--Radiotherapy, Digestive System Neoplasms--radiotherapy
- Abstract
Primary malignant tumors of the gastrointestinal tract account for 23% of all invasive cancers and 24% of all the deaths in 1988. In the United States, the American Cancer Society estimates that there will be 227500 new cases of gastrointestinal malignancy di agnosed, with 122350 deaths. This includes 9800 new cases of carcinomas of the esopha gus, 24800 carcinomas of the stomach, 2500 new cases of malignant tumors of the small intestine, 105000 new cases of tumors of the large intestine, and 42000 new cases of car cinoma of the rectum, 14000 new cases involving the liver and biliary passages, 27000 new cases of carcinoma of the pancreas, and 2400 other unspecified digestive tract ma lignancies. This combined incidence is second only to the number of new cases of lung cancer. Bleeding from the gastrointestinal tract represents one of the earliest findings with re gard to malignancy of the gastrointestinal tract. In general, personal or family history of colon and rectal cancer, personal or family history of polyps in the colon or rectum, or inflammatory bowel disease are high risk factors with regard to tumors in these loca tions. Dietary behavior is also important in that a diet high in fat and/or low in fiber content may be a significant causative factor.
- Published
- 2012
143. Cancer Associated Viruses
- Author
-
Erle S. Robertson and Erle S. Robertson
- Subjects
- Oncogenic viruses, Viral carcinogenesis
- Abstract
The acknowledgment that viruses are potent biological factors in driving many cancers have seen a dramatic upsurge in recent years in large part to the success of the human papilloma virus vaccine against invasive cervical carcinomas and followed by the awarding of the noble prize in medicine in 2008 to Dr. Harald zurHausen who identified the link between papilloma virus and cervical cancers. Over the last few years there have been some volumes addressing different aspects of viruses and cancers and to some extent focusing on the DNA viruses, more specifically the human DNA viruses. This proposed volume will attempt to review and address the major gaps in current knowledge in DNA viruses as well as RNA viruses bringing a historical perspective of where studies began to a more recent molecular approach and vaccine successes in tumor viruses. We will also cover other known oncogenic viruses associated cancers in other mammals in addition to humans.
- Published
- 2012
144. Steroid-Protein Interactions II
- Author
-
Ulrich Westphal and Ulrich Westphal
- Subjects
- Endocrinology, Biochemistry
- Published
- 2012
145. Arachidonic Acid Metabolism and Tumor Promotion
- Author
-
Susan M. Fischer, Thomas J. Slaga, Susan M. Fischer, and Thomas J. Slaga
- Subjects
- Cocarcinogenesis, Arachidonic acid--Metabolism, Arachidonic Acids--metabolism, Neoplasms--etiology
- Published
- 2012
146. Morphological Tumor Markers : General Aspects and Diagnostic Relevance
- Author
-
Gerhard Seifert and Gerhard Seifert
- Subjects
- Pathology, Cytology
- Abstract
New methods in immunocytochemistry and hybridization techniques enable the pathologist active in diagnosis to clarify more effectively problems in the classification and prognosis of tumors. By adopting these methods into his diagnostic repertoire it will be possible to create a closer, more productive connection between morphological diagnosis and clinical work. This volume gives the reader an up-to-date general survey from international experts of the method, technique and practical application of these new procedures.
- Published
- 2012
147. Urologic Oncology
- Author
-
Timothy L. Ratliff, William J. Catalona, Timothy L. Ratliff, and William J. Catalona
- Subjects
- Genitourinary organs--Cancer, Urogenital neoplasms
- Abstract
The study of genitourinary tumors is an area of recent rapid growth both in the understanding of disease processes and in the development of new diagnostic and therapeutic modalities. During rapid growth phases within any field, it is desirable to reflect on the current'state of the art'. It is difficult even for experts in reputed areas of advancement to distinguish true advances from false leads, but it is far more difficult yet for those whose expertise lies in other areas to evaluate important advances. Thus, an objective assessment of evolving areas of investigation in the form of a comprehensive review is of considerable value. we have attempted to provide the reader with an over In this volume, view of some of the current areas of investigation in urologic oncology by experts in each area. There often is a tendency for invited papers in books of this nature to lack important critical peer review and therefore, suffer from a lack of objectivity. We have attempted to diminish this problem by the selection of two experts to discuss each subject. We believe that this format has improved the overall quality of the book for two reasons: 1) the know ledge of each contributor that his or her work would be reviewed by a peer 2) the fact that contributions by encourages more rigorous scholarship, and two experts, including the individual insights of each, provides a better per spective for the reader.
- Published
- 2012
148. Immunobiology of Reproduction
- Author
-
Joan S. Hunt and Joan S. Hunt
- Subjects
- Reproduction--Immunological aspects--Congresse, Human reproduction--Immunological aspects--Con, Reproduction--immunology--congresses, Growth Substances--immunology--congresses
- Abstract
Over the last several decades, many biologists have been intrigued with the'immunological paradox'of pregnancy, where maternal and fetal tissues peaceably coexist despite their genetic differences. With the development of new insights on the interactive components of the immune system as well as the generation of powerful new molecular and cellular tools, singular progress has been made in understanding immunological events that culminate in successful pregnancy. This volume contains the proceedings for the first US symposium on the'Immunobiology of Reproduction'held August 26 - 29, 1993 in Boston, Massachusetts. Papers address hemotopoietic cells in reproductive tissues; growth factors/cytokines in the female reproductive tract and placenta; growth factor networks in pregnancy loss and cancer; placental expression of major histocompatibility complex and associated genes; experimental models of MHC gene expression; and immunological aspects of human infertility.
- Published
- 2012
149. Molecular Genetics and Therapy of Leukemia
- Author
-
Emil J. Freireich, Hagop Kantarjian, Emil J. Freireich, and Hagop Kantarjian
- Subjects
- Oncology, Cancer
- Published
- 2012
150. Biological and Hormonal Therapies of Cancer
- Author
-
Kenneth A. Foon, Hyman B. Muss, Kenneth A. Foon, and Hyman B. Muss
- Subjects
- Oncology, Cancer, Veterinary medicine
- Abstract
This volume, Biological and Hormonal Therapies of Cancer, which is part of the series Cancer Treatment and Research, presents selected new information concerning biologic and hormonal therapy of cancer. We have attempted to provide the reader with topics of major interest in a timely fashion. There is renewed interest in biologic therapy of cancer. Two chapters review the role of interferon in the hematologic malignancies and in solid tumors. Vaccine therapies have come to the forefront of cancer therapy re cently, and two chapters approach different strategies of vaccine therapies; one reviews the cellular vaccine therapies and another the anti-idiotype ap proach. The hormonal therapy chapters focus on current uses of endocrine therapy in endometrial, breast, and prostate cancer. In addition, hormonal strategies for the prevention of breast cancer and endometrial cancer, including excit ing information relating to phytochemicals, are presented. The effects of tamoxifen on endometrium is a topic of major interest and is discussed in detail. Finally, there is a chapter on estrogen receptor expression and regula tion in human breast cancer. These chapters are all written by experts in the field and contain timely and relevant information of interest to laboratory and clinical scientists and practitioners alike. Biologic and endocrine therapies represent major areas of cancer research interest. The advent of newer biologic therapies, including new antibody targeted treatments, and the use of biologics as tumor modulators to enhance the effects of other treatment regimens is an exploding avenue of research.
- Published
- 2012
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.