347 results on '"Ongkeko, Weg M."'
Search Results
2. The intratumor microbiome varies by geographical location and anatomical site in head and neck squamous cell carcinoma
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Yalamarty, Rishabh, Magesh, Shruti, John, Daniel, Chakladar, Jaideep, Li, Wei Tse, Brumund, Kevin T., Wang-Rodriguez, Jessica, and Ongkeko, Weg M.
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- 2024
- Full Text
- View/download PDF
3. The renal clear cell carcinoma immune landscape
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Saad, Omar A, Li, Wei Tse, Krishnan, Aswini R, Nguyen, Griffith C, Lopez, Jay P, McKay, Rana R, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Immunology ,Cancer ,Genetics ,Biotechnology ,Kidney Disease ,Human Genome ,Good Health and Well Being ,Biomarkers ,Carcinoma ,Renal Cell ,Disease Susceptibility ,Gene Expression Regulation ,Neoplastic ,Humans ,Immunity ,Kidney Neoplasms ,Signal Transduction ,Renal clear cell carcinoma ,TCGA ,Clinical Sciences ,Oncology & Carcinogenesis ,Clinical sciences ,Oncology and carcinogenesis - Abstract
A comprehensive evaluation of the clear cell renal cell carcinoma (ccRCC) immune landscape was found using 584 RNA-sequencing datasets from The Cancer Genome Atlas (TCGA), we identified 17 key dysregulated immune-associated genes in ccRCC based on association with clinical variables and important immune pathways. Of the numerous findings from our analyses, we found that several of the 17 key dysregulated genes are heavily involved in interleukin and NF-kB signaling and that somatic copy number alteration (SCNA) hotspots may be causally associated with gene dysregulation. More importantly, we also found that key immune-associated genes and pathways are strongly upregulated in ccRCC. Our study may lend novel insights into the clinical implications of immune dysregulation in ccRCC and suggests potential immunotherapeutic targets for further evaluation.
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- 2022
4. COVID-19 Severity Potentially Modulated by Cardiovascular-Disease-Associated Immune Dysregulation.
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Lee, Abby C, Castaneda, Grant, Li, Wei Tse, Chen, Chengyu, Shende, Neil, Chakladar, Jaideep, Taub, Pam R, Chang, Eric Y, and Ongkeko, Weg M
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Humans ,Cardiomyopathies ,Cytokines ,Lymphocyte Count ,Immunocompromised Host ,Coronary Artery Disease ,Venous Thromboembolism ,Inflammasomes ,Patient Acuity ,Datasets as Topic ,RNA-Seq ,COVID-19 ,cardiomyopathy ,coronary artery disease ,inflammation ,venous thromboembolism event ,Microbiology - Abstract
Patients with underlying cardiovascular conditions are particularly vulnerable to severe COVID-19. In this project, we aimed to characterize similarities in dysregulated immune pathways between COVID-19 patients and patients with cardiomyopathy, venous thromboembolism (VTE), or coronary artery disease (CAD). We hypothesized that these similarly dysregulated pathways may be critical to how cardiovascular diseases (CVDs) exacerbate COVID-19. To evaluate immune dysregulation in different diseases, we used four separate datasets, including RNA-sequencing data from human left ventricular cardiac muscle samples of patients with dilated or ischemic cardiomyopathy and healthy controls; RNA-sequencing data of whole blood samples from patients with single or recurrent event VTE and healthy controls; RNA-sequencing data of human peripheral blood mononuclear cells (PBMCs) from patients with and without obstructive CAD; and RNA-sequencing data of platelets from COVID-19 subjects and healthy controls. We found similar immune dysregulation profiles between patients with CVDs and COVID-19 patients. Interestingly, cardiomyopathy patients display the most similar immune landscape to COVID-19 patients. Additionally, COVID-19 patients experience greater upregulation of cytokine- and inflammasome-related genes than patients with CVDs. In all, patients with CVDs have a significant overlap of cytokine- and inflammasome-related gene expression profiles with that of COVID-19 patients, possibly explaining their greater vulnerability to severe COVID-19.
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- 2021
5. Chronic E-Cigarette Aerosol Inhalation Alters the Immune State of the Lungs and Increases ACE2 Expression, Raising Concern for Altered Response and Susceptibility to SARS-CoV-2
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Masso-Silva, Jorge A, Moshensky, Alexander, Shin, John, Olay, Jarod, Nilaad, Sedtavut, Advani, Ira, Bojanowski, Christine M, Crotty, Shane, Li, Wei Tse, Ongkeko, Weg M, Singla, Sunit, and Alexander, Laura E Crotty
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Pharmacology and Pharmaceutical Sciences ,Biomedical and Clinical Sciences ,Emerging Infectious Diseases ,Tobacco ,Tobacco Smoke and Health ,Prevention ,Biodefense ,Rare Diseases ,Electronic Nicotine Delivery Systems ,Lung ,Coronaviruses ,Infectious Diseases ,Aetiology ,2.1 Biological and endogenous factors ,Respiratory ,Inflammatory and immune system ,Good Health and Well Being ,e-cigarette ,vaping ,ACE2 ,COVID-19 ,immunomodulation ,SARS-CoV-2 ,RNAseq ,lipidomics ,Physiology ,Medical Physiology ,Psychology ,Biochemistry and cell biology ,Medical physiology - Abstract
Conventional smoking is known to both increase susceptibility to infection and drive inflammation within the lungs. Recently, smokers have been found to be at higher risk of developing severe forms of coronavirus disease 2019 (COVID-19). E-cigarette aerosol inhalation (vaping) has been associated with several inflammatory lung disorders, including the recent e-cigarette or vaping product use-associated lung injury (EVALI) epidemic, and recent studies have suggested that vaping alters host susceptibility to pathogens such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To assess the impact of vaping on lung inflammatory pathways, including the angiotensin-converting enzyme 2 (ACE2) receptor known to be involved in SARS-CoV-2 infection, mice were exposed to e-cigarette aerosols for 60 min daily for 1-6 months and underwent gene expression analysis. Hierarchical clustering revealed extensive gene expression changes occurred in the lungs of both inbred C57BL/6 mice and outbred CD1 mice, with 2,933 gene expression changes in C57BL/6 mice, and 2,818 gene expression changes in CD1 mice (>abs 1.25-fold change). Particularly, large reductions in IgA and CD4 were identified, indicating impairment of host responses to pathogens via reductions in immunoglobulins and CD4 T cells. CD177, facmr, tlr9, fcgr1, and ccr2 were also reduced, consistent with diminished host defenses via decreased neutrophils and/or monocytes in the lungs. Gene set enrichment (GSE) plots demonstrated upregulation of gene expression related to cell activation specifically in neutrophils. As neutrophils are a potential driver of acute lung injury in COVID-19, increased neutrophil activation in the lungs suggests that vapers are at higher risk of developing more severe forms of COVID-19. The receptor through which SARS-CoV-2 infects host cells, ACE2, was found to have moderate upregulation in mice exposed to unflavored vape pens, and further upregulation (six-fold) with JUUL mint aerosol exposure. No changes were found in mice exposed to unflavored Mod device-generated aerosols. These findings suggest that specific vaping devices and components of e-liquids have an effect on ACE2 expression, thus potentially increasing susceptibility to SARS-CoV-2. In addition, exposure to e-cigarette aerosols both with and without nicotine led to alterations in eicosanoid lipid profiles within the BAL. These data demonstrate that chronic, daily inhalation of e-cigarette aerosols fundamentally alters the inflammatory and immune state of the lungs. Thus, e-cigarette vapers may be at higher risk of developing infections and inflammatory disorders of the lungs.
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- 2021
6. Cardiovascular, cerebrovascular, and renal co-morbidities in COVID-19 patients: A systematic-review and meta-analysis
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Lee, Abby C, Li, Wei Tse, Apostol, Lauren, Ma, Jiayan, Taub, Pam R, Chang, Eric Y, Rajasekaran, Mahadevan, and Ongkeko, Weg M
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Information and Computing Sciences ,Biochemistry and Cell Biology ,Applied Computing ,Biological Sciences ,Cardiovascular ,Aging ,Hypertension ,Prevention ,Brain Disorders ,Kidney Disease ,Renal and urogenital ,Good Health and Well Being ,COVID-19 ,Comorbidity ,Meta-analysis ,Numerical and Computational Mathematics ,Computation Theory and Mathematics ,Biochemistry and cell biology ,Applied computing - Abstract
BackgroundCOVID-19 has infected over 35 million people worldwide and led to over 1 million deaths. Several risk factors that increase COVID-19 severity have emerged, including age and a history of cardiovascular disease, hypertension, or kidney disease. However, a number of outstanding questions persist, including whether the above comorbidities correlate with increased mortality from COVID-19 or whether age is a significant confounding variable that accounts for the observed relationship between COVID-19 severity and other comorbidities.Methods and findingsWe conducted a systematic review and meta-analysis of studies documenting COVID-19 patients with hypertension, cardiovascular disease, cerebrovascular disease, or chronic kidney disease. We classified COVID-19 cases into severe/non-severe or deceased/surviving and calculated the odds ratio (OR) for each of the four comorbidities in these cohorts. 36 studies, comprising 22,573 patients, are included in our meta-analysis. We found that hypertension is the most prevalent comorbidity in deceased COVID-19 patients (55.4%; CI: 49.4-61.3%), followed by cardiovascular disease (30.7%; CI: 22.6-38.8%), cerebrovascular disease (13.4%; CI: 9.12-19.2%), then chronic kidney disease (9.05%; CI: 5.57-15.0%). The risk of death is also significantly higher for patients with these comorbidities, with the greatest risk factor being chronic kidney disease (OR: 8.86; CI: 5.27-14.89), followed by cardiovascular disease (OR: 6.87; CI: 5.56-8.50), hypertension (OR: 4.87; CI: 4.19-5.66), and cerebrovascular disease (OR: 4.28; CI: 2.86-6.41). These risks are significantly higher than previously reported, while correlations between comorbidities and COVID-19 severity are similar to previously reported figures. Using meta-regression analysis with age as a moderating variable, we observed that age contributes to the observed risks but does not explain them fully.ConclusionsIn this meta-analysis, we observed that cardiovascular, cerebrovascular, and kidney-related comorbidities in COVID-19 significantly contributes to greater risk of mortality and increased disease severity. We also demonstrated that age may not be a confounder to these associations.
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- 2021
7. Redirecting extracellular proteases to molecularly guide radiosensitizing drugs to tumors
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Hingorani, Dina V, Crisp, Jessica L, Doan, Matthew K, Camargo, Maria F, Quraishi, Maryam A, Aguilera, Joseph, Gilardi, Mara, Gross, Larry A, Jiang, Tao, Li, Wei T, Ongkeko, Weg M, Cohen, Ezra EW, Gutkind, J Silvio, Adams, Stephen R, and Advani, Sunil J
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Rare Diseases ,Orphan Drug ,Cancer ,Biotechnology ,Radiation Oncology ,5.1 Pharmaceuticals ,Good Health and Well Being ,Cell Line ,Tumor ,Cell-Penetrating Peptides ,Drug Delivery Systems ,Humans ,Peptide Hydrolases ,Radiation-Sensitizing Agents ,Targeted drug delivery ,Cell penetrating peptides ,Antibody drug conjugates ,Radiosensitization ,Radiotherapy - Abstract
Patients with advanced cancers are treated with combined radiotherapy and chemotherapy, however curability is poor and treatment side effects severe. Drugs sensitizing tumors to radiotherapy have been developed to improve cell kill, but tumor specificity remains challenging. To achieve tumor selectivity of small molecule radiosensitizers, we tested as a strategy active tumor targeting using peptide-based drug conjugates. We attached an inhibitor of the DNA damage response to antibody or cell penetrating peptides. Antibody drug conjugates honed in on tumor overexpressed cell surface receptors with high specificity but lacked efficacy when conjugated to the DNA damage checkpoint kinase inhibitor AZD7762. As an alternative approach, we synthesized activatable cell penetrating peptide scaffolds that accumulated within tumors based on matrix metalloproteinase cleavage. While matrix metalloproteinases are integral to tumor progression, they have proven therapeutically elusive. We harnessed these pro-tumorigenic extracellular proteases to spatially guide radiosensitizer drug delivery using cleavable activatable cell penetrating peptides. Here, we tested the potential of these two drug delivery platforms targeting distinct tumor compartments in combination with radiotherapy and demonstrate the advantages of protease triggered cell penetrating peptide scaffolds over antibody drug conjugates to deliver small molecule amine radiosensitizers.
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- 2020
8. Randomised controlled trial of real-time feedback and brief coaching to reduce indoor smoking
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Hovell, Melbourne F, Bellettiere, John, Liles, Sandy, Nguyen, Benjamin, Berardi, Vincent, Johnson, Christine, Matt, Georg E, Malone, John, Boman-Davis, Marie C, Quintana, Penelope JE, Obayashi, Saori, Chatfield, Dale, Robinson, Robert, Blumberg, Elaine J, Ongkeko, Weg M, Klepeis, Neil E, and Hughes, Suzanne C
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Public Health ,Health Sciences ,Health Effects of Indoor Air Pollution ,Drug Abuse (NIDA only) ,Tobacco Smoke and Health ,Substance Misuse ,Tobacco ,Clinical Research ,Clinical Trials and Supportive Activities ,3.2 Interventions to alter physical and biological environmental risks ,Prevention of disease and conditions ,and promotion of well-being ,3.1 Primary prevention interventions to modify behaviours or promote wellbeing ,Stroke ,Cancer ,Cardiovascular ,Respiratory ,Good Health and Well Being ,Adult ,Air Pollution ,Indoor ,Child ,Child ,Preschool ,Feedback ,Female ,Humans ,Infant ,Interrupted Time Series Analysis ,Male ,Mentoring ,Nicotine ,Smoking Prevention ,Tobacco Smoke Pollution ,Tobacco Smoking ,Vaping ,Young Adult ,Fresh Air Research Group ,Carcinogens ,Harm Reduction ,Secondhand smoke - Abstract
BackgroundPrevious secondhand smoke (SHS) reduction interventions have provided only delayed feedback on reported smoking behaviour, such as coaching, or presenting results from child cotinine assays or air particle counters.DesignThis SHS reduction trial assigned families at random to brief coaching and continuous real-time feedback (intervention) or measurement-only (control) groups.ParticipantsWe enrolled 298 families with a resident tobacco smoker and a child under age 14.InterventionWe installed air particle monitors in all homes. For the intervention homes, immediate light and sound feedback was contingent on elevated indoor particle levels, and up to four coaching sessions used prompts and praise contingent on smoking outdoors. Mean intervention duration was 64 days.MeasuresThe primary outcome was 'particle events' (PEs) which were patterns of air particle concentrations indicative of the occurrence of particle-generating behaviours such as smoking cigarettes or burning candles. Other measures included indoor air nicotine concentrations and participant reports of particle-generating behaviour.ResultsPEs were significantly correlated with air nicotine levels (r=0.60) and reported indoor cigarette smoking (r=0.51). Interrupted time-series analyses showed an immediate intervention effect, with reduced PEs the day following intervention initiation. The trajectory of daily PEs over the intervention period declined significantly faster in intervention homes than in control homes. Pretest to post-test, air nicotine levels, cigarette smoking and e-cigarette use decreased more in intervention homes than in control homes.ConclusionsResults suggest that real-time particle feedback and coaching contingencies reduced PEs generated by cigarette smoking and other sources.Trial registration numberNCT01634334; Post-results.
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- 2020
9. The Landscape of Long Non-Coding RNA Dysregulation and Clinical Relevance in Muscle Invasive Bladder Urothelial Carcinoma.
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Shen, Haotian, Wong, Lindsay M, Li, Wei Tse, Chu, Megan, High, Rachel A, Chang, Eric Y, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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TCGA ,bladder carcinoma ,lncRNA-protein interaction ,lncRNAs ,Oncology and Carcinogenesis - Abstract
Bladder cancer is one of the most common cancers in the United States, but few advancements in treatment options have occurred in the past few decades. This study aims to identify the most clinically relevant long non-coding RNAs (lncRNAs) to serve as potential biomarkers and treatment targets for muscle invasive bladder cancer (MIBC). Using RNA-sequencing data from 406 patients in The Cancer Genome Atlas (TCGA) database, we identified differentially expressed lncRNAs in MIBC vs. normal tissues. We then associated lncRNA expression with patient survival, clinical variables, oncogenic signatures, cancer- and immune-associated pathways, and genomic alterations. We identified a panel of 20 key lncRNAs that were most implicated in MIBC prognosis after differential expression analysis and prognostic correlations. Almost all lncRNAs we identified are correlated significantly with oncogenic processes. In conclusion, we discovered previously undescribed lncRNAs strongly implicated in the MIBC disease course that may be leveraged for diagnostic and treatment purposes in the future. Functional analysis of these lncRNAs may also reveal distinct mechanisms of bladder cancer carcinogenesis.
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- 2019
10. Melanoma tumor microbiome as a predictor of anti-PD-1 and anti-CTLA-4 immunotherapy response.
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Uzelac, Matthew, primary, Li, Wei Tse, additional, Li, Yuxiang, additional, and Ongkeko, Weg M., additional
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- 2024
- Full Text
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11. Papillary Thyroid Carcinoma Variants are Characterized by Co-dysregulation of Immune and Cancer Associated Genes.
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Chakladar, Jaideep, Li, Wei Tse, Bouvet, Michael, Chang, Eric Y, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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cancer immunology ,microRNA ,papillary thyroid carcinoma ,Oncology and Carcinogenesis - Abstract
Papillary thyroid carcinoma (PTC) variants exhibit different prognosis, but critical characteristics of PTC variants that contribute to differences in pathogenesis are not well-known. This study aims to characterize dysregulated immune-associated and cancer-associated genes in three PTC subtypes to explore how the interplay between cancer and immune processes causes differential prognosis. RNA-sequencing data from The Cancer Genome Atlas (TCGA) were used to identify dysregulated genes in each variant. The dysregulation profiles of the subtypes were compared using functional pathways clustering and correlations to relevant clinical variables, genomic alterations, and microRNA regulation. We discovered that the dysregulation profiles of classical PTC (CPTC) and the tall cell variant (TCPTC) are similar and are distinct from that of the follicular variant (FVPTC). However, unique cancer or immune-associated genes are associated with clinical variables for each subtype. Cancer-related genes MUC1, FN1, and S100-family members were the most clinically relevant in CPTC, while APLN and IL16, both immune-related, were clinically relevant in FVPTC. RAET-family members, also immune-related, were clinically relevant in TCPTC. Collectively, our data suggest that dysregulation of both cancer and immune associated genes defines the gene expression landscapes of PTC variants, but different cancer or immune related genes may drive the phenotype of each variant.
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- 2019
12. Identification and characterization of dysregulated P-element induced wimpy testis-interacting RNAs in head and neck squamous cell carcinoma
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Saad, Maarouf A, Ku, Jonjei, Kuo, Selena Z, Li, Pin Xue, Zheng, Hao, Yu, Michael Andrew, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Dental/Oral and Craniofacial Disease ,Biotechnology ,Genetics ,Substance Misuse ,Alcoholism ,Alcohol Use and Health ,Cancer ,Aetiology ,2.1 Biological and endogenous factors ,Good Health and Well Being ,head and neck squamous cell carcinoma ,piwi-interacting RNA ,alcohol ,epigenetics ,Oncology and carcinogenesis - Abstract
It is clear that alcohol consumption is a major risk factor in the pathogenesis of head and neck squamous cell carcinoma (HNSCC); however, the molecular mechanism underlying the pathogenesis of alcohol-associated HNSCC remains poorly understood. The aim of the present study was to identify and characterize P-element-induced wimpy testis (PIWI)-interacting RNAs (piRNAs) and PIWI proteins dysregulated in alcohol-associated HNSCC to elucidate their function in the development of this cancer. Using next generation RNA-sequencing (RNA-seq) data obtained from 40 HNSCC patients, the piRNA and PIWI protein expression of HNSCC samples was compared between alcohol drinkers and non-drinkers. A separate piRNA expression RNA-seq analysis of 18 non-smoker HNSCC patients was also conducted. To verify piRNA expression, reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was performed on the most differentially expressed alcohol-associated piRNAs in ethanol and acetaldehyde-treated normal oral keratinocytes. The correlation between piRNA expression and patient survival was analyzed using Kaplan-Meier estimators and multivariate Cox proportional hazard models. A comparison between alcohol drinking and non-drinking HNSCC patients demonstrated that a panel of 3,223 piRNA transcripts were consistently detected and differentially expressed. RNA-seq analysis and in vitro RT-qPCR verification revealed that 4 of these piRNAs, piR-35373, piR-266308, piR-58510 and piR-38034, were significantly dysregulated between drinking and non-drinking cohorts. Of these four piRNAs, low expression of piR-58510 and piR-35373 significantly correlated with improved patient survival. Furthermore, human PIWI-like protein 4 was consistently upregulated in ethanol and acetaldehyde-treated normal oral keratinocytes. These results demonstrate that alcohol consumption may cause dysregulation of piRNA expression in HNSCC and in vitro verifications identified 4 piRNAs that may be involved in the pathogenesis of alcohol-associated HNSCC.
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- 2019
13. Medical student’s perception of the COVID-19 pandemic effect on their education and well-being: a cross-sectional survey in the United States
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Chakladar, Jaideep, Diomino, Anthony, Li, Wei Tse, Tsai, Joseph C., Krishnan, Aswini R., Zou, Angela E., Kharidia, Khush, Baig, Farhan A., Householder, Sarah, Kuo, Selena Z., Chandrasekar, Shyam, Chang, Eric Y., and Ongkeko, Weg M.
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- 2022
- Full Text
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14. Functional Genomics Profiling of Bladder Urothelial Carcinoma MicroRNAome as a Potential Biomarker
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Li, Wei Tse, Zheng, Hao, Nguyen, Vincent, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Prevention ,Tobacco ,Cancer ,Human Genome ,Clinical Research ,Tobacco Smoke and Health ,Urologic Diseases ,Biotechnology ,Genetics ,2.1 Biological and endogenous factors ,Aetiology ,Detection ,screening and diagnosis ,4.1 Discovery and preclinical testing of markers and technologies ,Good Health and Well Being ,Biomarkers ,Tumor ,Carcinoma ,Female ,Gene Expression Profiling ,Gene Expression Regulation ,Neoplastic ,Genomics ,Humans ,Male ,MicroRNAs ,Urinary Bladder ,Urinary Bladder Neoplasms ,Clinical Sciences ,Oncology & Carcinogenesis ,Clinical sciences ,Oncology and carcinogenesis - Abstract
Though bladder urothelial carcinoma is the most common form of bladder cancer, advances in its diagnosis and treatment have been modest in the past few decades. To evaluate miRNAs as putative disease markers for bladder urothelial carcinoma, this study develops a process to identify dysregulated miRNAs in cancer patients and potentially stratify patients based on the association of their microRNAome phenotype to genomic alterations. Using RNA sequencing data for 409 patients from the Cancer Genome Atlas, we examined miRNA differential expression between cancer and normal tissues and associated differentially expressed miRNAs with patient survival and clinical variables. We then correlated miRNA expressions with genomic alterations using the Wilcoxon test and REVEALER. We found a panel of six miRNAs dysregulated in bladder cancer and exhibited correlations to patient survival. We also performed differential expression analysis and clinical variable correlations to identify miRNAs associated with tobacco smoking, the most important risk factor for bladder cancer. Two miRNAs, miR-323a and miR-431, were differentially expressed in smoking patients compared to nonsmoking patients and were associated with primary tumor size. Functional studies of these miRNAs and the genomic features we identified for potential stratification may reveal underlying mechanisms of bladder cancer carcinogenesis and further diagnosis and treatment methods for urothelial bladder carcinoma.
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- 2018
15. Computational methods reveal novel functionalities of PIWI-interacting RNAs in human papillomavirus-induced head and neck squamous cell carcinoma
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Krishnan, Aswini R, Qu, Yuanhao, Li, Pin Xue, Zou, Angela E, Califano, Joseph A, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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Cervical Cancer ,Sexually Transmitted Infections ,Cancer ,Infectious Diseases ,Dental/Oral and Craniofacial Disease ,Rare Diseases ,Genetics ,Underpinning research ,2.1 Biological and endogenous factors ,Aetiology ,1.1 Normal biological development and functioning ,piRNA ,HNSCC ,ncRNA ,HPV ,Oncology and Carcinogenesis - Abstract
Human papillomavirus (HPV) infection is the fastest growing cause of head and neck squamous cell carcinoma (HNSCC) today, but its role in malignant transformation remains unclear. This study aimed to conduct a comprehensive investigation of PIWI-interacting RNA (piRNA) alterations and functionalities in HPV-induced HNSCC. Using 77 RNA-sequencing datasets from TCGA, we examined differential expression of piRNAs between HPV16(+) HNSCC and HPV(-) Normal samples, identifying a panel of 30 HPV-dysregulated piRNAs. We then computationally investigated the potential mechanistic significances of these transcripts in HPV-induced HNSCC, identifying our panel of piRNAs to associate with the protein PIWIL4 as well as the RTL family of retrotransposon-like genes, possibly through direct binding interactions. We also recognized several HPV-dysregulated transcripts for their correlations with well-documented mutations and copy number variations in HNSCC as well as HNSCC clinical variables, demonstrating the potential ability of our piRNAs to play important roles in large-scale modulation of HNSCC in addition to their direct, smaller-scale interactions in this malignancy. The differential expression of key piRNAs, including NONHSAT077364, NONHSAT102574, and NONHSAT128479, was verified in vitro by evaluating endogenous expression in HPV(+) cancer vs. HPV(-) normal cell lines. Overall, our novel study provides a rigorous investigation of piRNA dysregulation in HPV-related HNSCC, and lends critical insight into the idea that these small regulatory transcripts may play crucial and previously unidentified roles in tumor pathogenesis and progression.
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- 2018
16. Microbiome Dysbiosis Is Associated with Castration Resistance and Cancer Stemness in Metastatic Prostate Cancer
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Uzelac, Matthew, primary, Xin, Ruomin, additional, and Ongkeko, Weg M., additional
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- 2024
- Full Text
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17. Microbiome Dysbiosis Associates to Castration Resistance and Cancer Stemness in Metastatic Prostate Cancer
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Uzelac, Matthew, primary, Xin, Ruomin, additional, and Ongkeko, Weg M., additional
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- 2024
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18. Urinary Microbiome Dysbiosis and Immune Dysregulations as Potential Diagnostic Indicators of Bladder Cancer
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Uzelac, Matthew, primary, Xin, Ruomin, additional, Chen, Tianyi, additional, John, Daniel, additional, Li, Wei Tse, additional, Rajasekaran, Mahadevan, additional, and Ongkeko, Weg M., additional
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- 2024
- Full Text
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19. Analysis of the immune landscape in virus-induced cancers using a novel integrative mechanism discovery approach
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Wong, Lindsay M., Li, Wei Tse, Shende, Neil, Tsai, Joseph C., Ma, Jiayan, Chakladar, Jaideep, Gnanasekar, Aditi, Qu, Yuanhao, Dereschuk, Kypros, Wang-Rodriguez, Jessica, and Ongkeko, Weg M.
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- 2021
- Full Text
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20. Cardiovascular, cerebrovascular, and renal co-morbidities in COVID-19 patients: A systematic-review and meta-analysis
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Lee, Abby C., Li, Wei Tse, Apostol, Lauren, Ma, Jiayan, Taub, Pam R., Chang, Eric Y., Rajasekaran, Mahadevan, and Ongkeko, Weg M.
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- 2021
- Full Text
- View/download PDF
21. The intratumor microbiome predicts prognosis across gender and subtypes in papillary thyroid carcinoma
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Gnanasekar, Aditi, Castaneda, Grant, Iyangar, Anjali, Magesh, Shruti, Perez, Daisy, Chakladar, Jaideep, Li, Wei Tse, Bouvet, Michael, Chang, Eric Y., and Ongkeko, Weg M.
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- 2021
- Full Text
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22. A comprehensive study of smoking-specific microRNA alterations in head and neck squamous cell carcinoma
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Krishnan, Aswini R, Zheng, Hao, Kwok, James G, Qu, Yuanhao, Zou, Angela E, Korrapati, Avinaash, Li, Pin Xue, Califano, Joseph A, Hovell, Melbourne F, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Dentistry ,Tobacco Smoke and Health ,Tobacco ,Prevention ,Cancer ,Rare Diseases ,Dental/Oral and Craniofacial Disease ,Biotechnology ,Genetics ,2.1 Biological and endogenous factors ,Aetiology ,Good Health and Well Being ,Carcinoma ,Squamous Cell ,Head and Neck Neoplasms ,Humans ,MicroRNAs ,Sequence Analysis ,RNA ,Smoking ,Squamous Cell Carcinoma of Head and Neck ,Head and neck neoplasms ,RNA ,Untranslated ,Public Health and Health Services ,Oncology & Carcinogenesis ,Oncology and carcinogenesis - Abstract
ObjectiveWhile tobacco smoking is a well-known risk factor for head and neck squamous cell carcinoma (HNSCC), the molecular mechanisms underlying tobacco-induced HNSCC remain unclear. This study sought to comprehensively identify microRNA (miRNA) alterations and evaluate their clinical relevance in smoking-induced HNSCC pathogenesis and progression.Materials and methodsUsing small RNA-sequencing data and clinical data from 145 HNSCC patients, we performed a series of differential expression and correlation analyses to identify a panel of tobacco-dysregulated miRNAs associated with key clinical characteristics in HNSCC. We then examined the expression patterns of these miRNAs in normal epithelial cell lines following exposure to cigarette smoke extract.ResultsOur analyses revealed distinct panels of miRNAs to be dysregulated with smoking status and associated with additional clinical features, including tumor stage, metastasis, anatomic site, and patient survival. The differential expression of key miRNAs, including miR-101, miR-181b, miR-486, and miR-1301, was verified in cigarette-treated epithelial cell lines, suggesting their potential roles in the early development of smoking-related HNSCCs.ConclusionSpecific alterations in miRNA expression may be traced to tobacco use and are associated with important HNSCC clinical characteristics. Future studies of these miRNAs may be valuable for furthering the understanding and targeted treatment of smoking-associated HNSCC.
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- 2017
23. Smoking status regulates a novel panel of PIWI-interacting RNAs in head and neck squamous cell carcinoma.
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Krishnan, Aswini R, Korrapati, Avinaash, Zou, Angela E, Qu, Yuanhao, Wang, Xiao Qi, Califano, Joseph A, Wang-Rodriguez, Jessica, Lippman, Scott M, Hovell, Melbourne F, and Ongkeko, Weg M
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Humans ,Carcinoma ,Squamous Cell ,Head and Neck Neoplasms ,RNA ,Small Interfering ,Smoking ,Female ,Male ,Squamous Cell Carcinoma of Head and Neck ,Head and neck neoplasms ,RNA ,Small interfering ,Cancer ,Biotechnology ,Genetics ,Dental/Oral and Craniofacial Disease ,Human Genome ,Tobacco ,Rare Diseases ,Tobacco Smoke and Health ,Good Health and Well Being ,Dentistry ,Oncology and Carcinogenesis ,Public Health and Health Services ,Oncology & Carcinogenesis - Abstract
ObjectiveSmoking remains a primary etiological factor in head and neck squamous cell carcinoma (HNSCC). Given that non-coding RNAs (ncRNAs), including PIWI-interacting RNAs (piRNAs), have emerged as mediators of initiation and progression in head and neck malignancies, we undertook a global study of piRNA expression patterns in smoking-associated HNSCC.Materials and methodsUsing RNA-sequencing data from 256 current smoker and lifelong nonsmoker samples in The Cancer Genome Atlas (TCGA), we analyzed the differential expression patterns of 27,127 piRNAs across patient cohorts stratified by tobacco use, with HPV16 status and tumor status taken into account. We correlated their expression to clinical characteristics and to smoking-induced alterations of PIWI proteins, the functional counterparts of piRNAs. Finally, we correlated our identified piRNAs and PIWI proteins to known chromosomal aberrations in HNSCC to understand their wider-ranging genomic effects.Results and conclusionOur analyses implicated a 13-member piRNA panel in smoking-related HNSCC, among which NONHSAT123636 and NONHSAT113708 associated with tumor stage, NONHSAT067200 with patient survival, and NONHSAT081250 with smoking-altered PIWIL1 protein expression. 6 piRNAs as well as PIWIL1 correlated with genomic alterations common to HNSCC, including TP53 mutation, TP53-3p co-occurrence, and 3q26, 8q24, and 11q13 amplification. Collectively, our findings provide novel insights into the etiology-specific piRNA landscape of smoking-induced HNSCC.
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- 2017
24. Alcohol-dysregulated microRNAs in hepatitis B virus-related hepatocellular carcinoma.
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Zheng, Hao, Zou, Angela E, Saad, Maarouf A, Wang, Xiao Qi, Kwok, James G, Korrapati, Avinaash, Li, Pinxue, Kisseleva, Tatiana, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
- Subjects
Humans ,Hepatitis B virus ,Carcinoma ,Hepatocellular ,Liver Neoplasms ,MicroRNAs ,Polymerase Chain Reaction ,Alcohol Drinking ,Carcinoma ,Hepatocellular ,General Science & Technology - Abstract
Alcohol consumption and chronic hepatitis B virus (HBV) infection are two well-established risk factors for Hepatocellular carcinoma (HCC); however, there remains a limited understanding of the molecular pathway behind the pathogenesis and progression behind HCC, and how alcohol promotes carcinogenesis in the context of HBV+ HCC. Using next-generation sequencing data from 130 HCC patients and 50 normal liver tissues, we identified a panel of microRNAs that are significantly dysregulated by alcohol consumption in HBV+ patients. In particular, two microRNAs, miR-944 and miR-223-3p, showed remarkable correlation with clinical indication and genomic alterations. We confirmed the dysregulation of these two microRNAs in liver cell lines treated by alcohol and acetaldehyde, and showed that manipulation of miR-223-3p and miR-944 expression induces significant changes in cellular proliferation, sensitivity to doxorubicin, and the expression of both direct-binding and downstream mRNA targets. Together, the results of this study suggest that alcohol consumption in HBV+ HCCs regulates microRNAs that likely play previously uncharacterized roles in the alcohol-associated carcinogenesis of HCC, and future studies of these microRNAs may be valuable for furthering the understanding and treatment of alcohol and HBV-associated HCC.
- Published
- 2017
25. Redirecting extracellular proteases to molecularly guide radiosensitizing drugs to tumors
- Author
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Hingorani, Dina V., Crisp, Jessica L., Doan, Matthew K., Camargo, Maria F., Quraishi, Maryam A., Aguilera, Joseph, Gilardi, Mara, Gross, Larry A., Jiang, Tao, Li, Wei T., Ongkeko, Weg M., Cohen, Ezra E.W., Gutkind, J. Silvio, Adams, Stephen R., and Advani, Sunil J.
- Published
- 2020
- Full Text
- View/download PDF
26. The non-coding landscape of head and neck squamous cell carcinoma
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Zou, Angela E, Zheng, Hao, Saad, Maarouf A, Rahimy, Mehran, Ku, Jonjei, Kuo, Selena Z, Honda, Thomas K, Wang-Rodriguez, Jessica, Xuan, Yinan, Korrapati, Avinaash, Yu, Vicky, Singh, Pranav, Grandis, Jennifer R, King, Charles C, Lippman, Scott M, Wang, Xiao Qi, Hinton, Andrew, and Ongkeko, Weg M
- Subjects
Dental/Oral and Craniofacial Disease ,Cancer ,Human Genome ,Rare Diseases ,Genetics ,Biotechnology ,Good Health and Well Being ,Adult ,Aged ,Aged ,80 and over ,Carcinoma ,Squamous Cell ,Cell Line ,Tumor ,Female ,Gene Expression Profiling ,Gene Expression Regulation ,Neoplastic ,Head and Neck Neoplasms ,Humans ,Male ,MicroRNAs ,Middle Aged ,RNA ,Long Noncoding ,RNA ,Untranslated ,Sequence Analysis ,RNA ,Squamous Cell Carcinoma of Head and Neck ,Transcriptome ,head and neck cancer ,non-coding RNA ,RNA-sequencing ,cancer transcriptomics ,Oncology and Carcinogenesis - Abstract
Head and neck squamous cell carcinoma (HNSCC) is an aggressive disease marked by frequent recurrence and metastasis and stagnant survival rates. To enhance molecular knowledge of HNSCC and define a non-coding RNA (ncRNA) landscape of the disease, we profiled the transcriptome-wide dysregulation of long non-coding RNA (lncRNA), microRNA (miRNA), and PIWI-interacting RNA (piRNA) using RNA-sequencing data from 422 HNSCC patients in The Cancer Genome Atlas (TCGA). 307 non-coding transcripts differentially expressed in HNSCC were significantly correlated with patient survival, and associated with mutations in TP53, CDKN2A, CASP8, PRDM9, and FBXW7 and copy number variations in chromosomes 3, 5, 7, and 18. We also observed widespread ncRNA correlation to concurrent TP53 and chromosome 3p loss, a compelling predictor of poor prognosis in HNSCCs. Three selected ncRNAs were additionally associated with tumor stage, HPV status, and other clinical characteristics, and modulation of their expression in vitro reveals differential regulation of genes involved in epithelial-mesenchymal transition and apoptotic response. This comprehensive characterization of the HNSCC non-coding transcriptome introduces new layers of understanding for the disease, and nominates a novel panel of transcripts with potential utility as prognostic markers or therapeutic targets.
- Published
- 2016
27. Electronic cigarette inhalation alters innate immunity and airway cytokines while increasing the virulence of colonizing bacteria.
- Author
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Hwang, John H, Lyes, Matthew, Sladewski, Katherine, Enany, Shymaa, McEachern, Elisa, Mathew, Denzil P, Das, Soumita, Moshensky, Alexander, Bapat, Sagar, Pride, David T, Ongkeko, Weg M, and Crotty Alexander, Laura E
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Neutrophils ,Macrophages ,Alveolar ,Epithelial Cells ,Animals ,Humans ,Mice ,Biofilms ,Tobacco ,Pneumonia ,Bacterial ,Disease Models ,Animal ,Antimicrobial Cationic Peptides ,Complex Mixtures ,Cytokines ,Smoke ,Cell Death ,Dose-Response Relationship ,Drug ,Female ,Immunity ,Innate ,Methicillin-Resistant Staphylococcus aureus ,Electronic Nicotine Delivery Systems ,Antimicrobial peptide LL-37 ,Cytotoxicity ,E-cigarette vapor ,Inflammatory lung disease ,MRSA pneumonia ,Staphylococcal virulence ,Infectious Diseases ,Tobacco Smoke and Health ,Lung ,Biodefense ,Prevention ,Emerging Infectious Diseases ,Vaccine Related ,2.1 Biological and endogenous factors ,Respiratory ,Infection ,Immunology ,Medicinal and Biomolecular Chemistry - Abstract
UnlabelledElectronic (e)-cigarette use is rapidly rising, with 20 % of Americans ages 25-44 now using these drug delivery devices. E-cigarette users expose their airways, cells of host defense, and colonizing bacteria to e-cigarette vapor (EV). Here, we report that exposure of human epithelial cells at the air-liquid interface to fresh EV (vaped from an e-cigarette device) resulted in dose-dependent cell death. After exposure to EV, cells of host defense-epithelial cells, alveolar macrophages, and neutrophils-had reduced antimicrobial activity against Staphylococcus aureus (SA). Mouse inhalation of EV for 1 h daily for 4 weeks led to alterations in inflammatory markers within the airways and elevation of an acute phase reactant in serum. Upon exposure to e-cigarette vapor extract (EVE), airway colonizer SA had increased biofilm formation, adherence and invasion of epithelial cells, resistance to human antimicrobial peptide LL-37, and up-regulation of virulence genes. EVE-exposed SA were more virulent in a mouse model of pneumonia. These data suggest that e-cigarettes may be toxic to airway cells, suppress host defenses, and promote inflammation over time, while also promoting virulence of colonizing bacteria.Key messageAcute exposure to e-cigarette vapor (EV) is cytotoxic to airway cells in vitro. Acute exposure to EV decreases macrophage and neutrophil antimicrobial function. Inhalation of EV alters immunomodulating cytokines in the airways of mice. Inhalation of EV leads to increased markers of inflammation in BAL and serum. Staphylococcus aureus become more virulent when exposed to EV.
- Published
- 2016
28. Electronic cigarettes induce DNA strand breaks and cell death independently of nicotine in cell lines
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Yu, Vicky, Rahimy, Mehran, Korrapati, Avinaash, Xuan, Yinan, Zou, Angela E, Krishnan, Aswini R, Tsui, Tzuhan, Aguilera, Joseph A, Advani, Sunil, Crotty Alexander, Laura E, Brumund, Kevin T, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
- Subjects
Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Rare Diseases ,Cancer ,Genetics ,Dental/Oral and Craniofacial Disease ,Tobacco ,2.2 Factors relating to the physical environment ,Carcinoma ,Squamous Cell ,Cell Death ,Cell Line ,Tumor ,DNA Damage ,Electronic Nicotine Delivery Systems ,Epithelial Cells ,Head and Neck Neoplasms ,Humans ,Nicotine ,Nicotinic Agonists ,Volatilization ,Oral cancer ,Head and neck squamous cell carcinoma ,Electronic cigarettes ,Smoking ,DNA damage ,Strand breaks ,Dentistry ,Public Health and Health Services ,Oncology & Carcinogenesis ,Oncology and carcinogenesis - Abstract
ObjectivesEvaluate the cytotoxicity and genotoxicity of short- and long-term e-cigarette vapor exposure on a panel of normal epithelial and head and neck squamous cell carcinoma (HNSCC) cell lines.Materials and methodsHaCaT, UMSCC10B, and HN30 were treated with nicotine-containing and nicotine-free vapor extract from two popular e-cigarette brands for periods ranging from 48 h to 8 weeks. Cytotoxicity was assessed using Annexin V flow cytometric analysis, trypan blue exclusion, and clonogenic assays. Genotoxicity in the form of DNA strand breaks was quantified using the neutral comet assay and γ-H2AX immunostaining.ResultsE-cigarette-exposed cells showed significantly reduced cell viability and clonogenic survival, along with increased rates of apoptosis and necrosis, regardless of e-cigarette vapor nicotine content. They also exhibited significantly increased comet tail length and accumulation of γ-H2AX foci, demonstrating increased DNA strand breaks.ConclusionE-cigarette vapor, both with and without nicotine, is cytotoxic to epithelial cell lines and is a DNA strand break-inducing agent. Further assessment of the potential carcinogenic effects of e-cigarette vapor is urgently needed.
- Published
- 2016
29. Alcohol-dysregulated miR-30a and miR-934 in head and neck squamous cell carcinoma.
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Saad, Maarouf A, Kuo, Selena Z, Rahimy, Elham, Zou, Angela E, Korrapati, Avinaash, Rahimy, Mehran, Kim, Elizabeth, Zheng, Hao, Yu, Michael Andrew, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
- Subjects
Cell Line ,Tumor ,Humans ,Carcinoma ,Squamous Cell ,Head and Neck Neoplasms ,Alcohols ,Ethanol ,Acetaldehyde ,MicroRNAs ,Reverse Transcriptase Polymerase Chain Reaction ,Apoptosis ,Cell Proliferation ,Gene Expression Regulation ,Neoplastic ,Adult ,Middle Aged ,Female ,Male ,Squamous Cell Carcinoma of Head and Neck ,Head and neck squamous cell carcinoma ,microRNA ,RNA-sequencing ,Alcohol ,Cell Line ,Tumor ,Carcinoma ,Squamous Cell ,Gene Expression Regulation ,Neoplastic ,Oncology & Carcinogenesis ,Oncology and Carcinogenesis - Abstract
BackgroundAlcohol consumption is a well-established risk factor for head and neck squamous cell carcinoma (HNSCC); however, the molecular mechanisms by which alcohol promotes HNSCC pathogenesis and progression remain poorly understood. Our study sought to identify microRNAs that are dysregulated in alcohol-associated HNSCC and investigate their contribution to the malignant phenotype.MethodUsing RNA-sequencing data from 136 HNSCC patients, we compared the expression levels of 1,046 microRNAs between drinking and non-drinking cohorts. Dysregulated microRNAs were verified by qRT-PCR in normal oral keratinocytes treated with biologically relevant doses of ethanol and acetaldehyde. The most promising microRNA candidates were investigated for their effects on cellular proliferation and invasion, sensitivity to cisplatin, and expression of cancer stem cell genes. Finally, putative target genes were identified and evaluated in vitro to further establish roles for these miRNAs in alcohol-associated HNSCC.ResultsFrom RNA-sequencing analysis we identified 8 miRNAs to be significantly upregulated in alcohol-associated HNSCCs. qRT-PCR experiments determined that among these candidates, miR-30a and miR-934 were the most highly upregulated in vitro by alcohol and acetaldehyde. Overexpression of miR-30a and miR-934 in normal and HNSCC cell lines produced up to a 2-fold increase in cellular proliferation, as well as induction of the anti-apoptotic gene BCL-2. Upon inhibition of these miRNAs, HNSCC cell lines exhibited increased sensitivity to cisplatin and reduced matrigel invasion. miRNA knockdown also indicated direct targeting of several tumor suppressor genes by miR-30a and miR-934.ConclusionsAlcohol induces the dysregulation of miR-30a and miR-934, which may play crucial roles in HNSCC pathogenesis and progression. Future investigation of the alcohol-mediated pathways effecting these transformations will prove valuable for furthering the understanding and treatment of alcohol-associated HNSCC.
- Published
- 2015
30. Transcriptome sequencing uncovers novel long noncoding and small nucleolar RNAs dysregulated in head and neck squamous cell carcinoma
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Zou, Angela E, Ku, Jonjei, Honda, Thomas K, Yu, Vicky, Kuo, Selena Z, Zheng, Hao, Xuan, Yinan, Saad, Maarouf A, Hinton, Andrew, Brumund, Kevin T, Lin, Jonathan H, Wang-Rodriguez, Jessica, and Ongkeko, Weg M
- Subjects
Biological Sciences ,Bioinformatics and Computational Biology ,Rare Diseases ,Genetics ,Stem Cell Research ,Cancer ,Biotechnology ,Dental/Oral and Craniofacial Disease ,Stem Cell Research - Nonembryonic - Human ,Aetiology ,2.1 Biological and endogenous factors ,Adult ,Aged ,Aged ,80 and over ,Carcinoma ,Squamous Cell ,Cell Line ,Tumor ,Cell Movement ,Cell Proliferation ,Epithelial-Mesenchymal Transition ,Female ,Gene Expression Profiling ,Gene Expression Regulation ,Neoplastic ,Head and Neck Neoplasms ,High-Throughput Nucleotide Sequencing ,Humans ,Male ,Middle Aged ,RNA ,Long Noncoding ,RNA ,Small Nucleolar ,Sequence Analysis ,RNA ,Survival Analysis ,HNSCC ,long noncoding RNAs ,RNA-sequencing ,small nucleolar RNAs ,Biochemistry and Cell Biology ,Developmental Biology ,Biochemistry and cell biology - Abstract
Head and neck squamous cell carcinoma persists as one of the most common and deadly malignancies, with early detection and effective treatment still posing formidable challenges. To expand our currently sparse knowledge of the noncoding alterations involved in the disease and identify potential biomarkers and therapeutic targets, we globally profiled the dysregulation of small nucleolar and long noncoding RNAs in head and neck tumors. Using next-generation RNA-sequencing data from 40 pairs of tumor and matched normal tissues, we found 2808 long noncoding RNA (lncRNA) transcripts significantly differentially expressed by a fold change magnitude ≥2. Meanwhile, RNA-sequencing analysis of 31 tumor-normal pairs yielded 33 significantly dysregulated small nucleolar RNAs (snoRNA). In particular, we identified two dramatically down-regulated lncRNAs and one down-regulated snoRNA whose expression levels correlated significantly with overall patient survival, suggesting their functional significance and clinical relevance in head and neck cancer pathogenesis. We confirmed the dysregulation of these noncoding RNAs in head and neck cancer cell lines derived from different anatomic sites, and determined that ectopic expression of the two lncRNAs inhibited key EMT and stem cell genes and reduced cellular proliferation and migration. As a whole, noncoding RNAs are pervasively dysregulated in head and squamous cell carcinoma. The precise molecular roles of the three transcripts identified warrants further characterization, but our data suggest that they are likely to play substantial roles in head and neck cancer pathogenesis and are significantly associated with patient survival.
- Published
- 2015
31. Parathyroid hormone related-protein promotes epithelial-to-mesenchymal transition in prostate cancer.
- Author
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Ongkeko, Weg M, Burton, Doug, Kiang, Alan, Abhold, Eric, Kuo, Selena Z, Rahimy, Elham, Yang, Meng, Hoffman, Robert M, Wang-Rodriguez, Jessica, and Deftos, Leonard J
- Subjects
Bone and Bones ,Cell Line ,Tumor ,Animals ,Humans ,Mice ,Mice ,Nude ,Mice ,SCID ,Prostatic Neoplasms ,Vimentin ,Parathyroid Hormone-Related Protein ,Cadherins ,Protein Isoforms ,Transcription Factors ,Microscopy ,Fluorescence ,Transplantation ,Heterologous ,Reverse Transcriptase Polymerase Chain Reaction ,Gene Expression Regulation ,Neoplastic ,RNA Interference ,Male ,Matrix Metalloproteinase 9 ,Epithelial-Mesenchymal Transition ,Snail Family Transcription Factors ,Cell Line ,Tumor ,Gene Expression Regulation ,Neoplastic ,Nude ,SCID ,Microscopy ,Fluorescence ,Transplantation ,Heterologous ,General Science & Technology - Abstract
Parathyroid hormone-related protein (PTHrP) possesses a variety of physiological and developmental functions and is also known to facilitate the progression of many common cancers, notably their skeletal invasion, primarily by increasing bone resorption. The purpose of this study was to determine whether PTHrP could promote epithelial-to-mesenchymal transition (EMT), a process implicated in cancer stem cells that is critically involved in cancer invasion and metastasis. EMT was observed in DU 145 prostate cancer cells stably overexpressing either the 1-141 or 1-173 isoform of PTHrP, where there was upregulation of Snail and vimentin and downregulation of E-cadherin relative to parental DU 145. By contrast, the opposite effect was observed in PC-3 prostate cancer cells where high levels of PTHrP were knocked-down via lentiviral siRNA transduction. Increased tumor progression was observed in PTHrP-overexpressing DU 145 cells while decreased progression was observed in PTHrP-knockdown PC-3 cells. PTHrP-overexpressing DU 145 formed larger tumors when implanted orthoptopically into nude mice and in one case resulted in spinal metastasis, an effect not observed among mice injected with parental DU 145 cells. PTHrP-overexpressing DU 145 cells also caused significant bone destruction when injected into the tibiae of nude mice, while parental DU 145 cells caused little to no destruction of bone. Together, these results suggest that PTHrP may work through EMT to promote an aggressive and metastatic phenotype in prostate cancer, a pathway of importance in cancer stem cells. Thus, continued efforts to elucidate the pathways involved in PTHrP-induced EMT as well as to develop ways to specifically target PTHrP signaling may lead to more effective therapies for prostate cancer.
- Published
- 2014
32. Salinomycin induces cell death and differentiation in head and neck squamous cell carcinoma stem cells despite activation of epithelial-mesenchymal transition and Akt
- Author
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Kuo, Selena Z, Blair, Katherine J, Rahimy, Elham, Kiang, Alan, Abhold, Eric, Fan, Jian-Bing, Wang-Rodriguez, Jessica, Altuna, Xabier, and Ongkeko, Weg M
- Abstract
Abstract Background Cancer stem cells (CSC) are believed to play a crucial role in cancer recurrence due to their resistance to conventional chemotherapy and capacity for self-renewal. Recent studies have reported that salinomycin, a livestock antibiotic, selectively targets breast cancer stem cells 100-fold more effectively than paclitaxel. In our study we sought to determine the effects of salinomycin on head and neck squamous cell carcinoma (HNSCC) stem cells. Methods MTS and TUNEL assays were used to study cell proliferation and apoptosis as a function of salinomycin exposure in JLO-1, a putative HNSCC stem cell culture. MTS and trypan blue dye exclusion assays were performed to investigate potential drug interactions between salinomycin and cisplatin or paclitaxel. Stem cell-like phenotype was measured by mRNA expression of stem cell markers, sphere-forming capacity, and matrigel invasion assays. Immunoblotting was also used to determine expression of epithelial-mesenchymal transition (EMT) markers and Akt phosphorylation. Arrays by Illumina, Inc. were used to profile microRNA expression as a function of salinomycin dose. Results In putative HNSCC stem cells, salinomycin was found to significantly inhibit cell viability, induce a 71.5% increase in levels of apoptosis, elevate the Bax/Bcl-2 ratio, and work synergistically with cisplatin and paclitaxel in inducing cell death. It was observed that salinomycin significantly inhibited sphere forming-capability and repressed the expression of CD44 and BMI-1 by 3.2-fold and 6.2-fold, respectively. Furthermore, salinomycin reduced invasion of HNSCC stem cells by 2.1 fold. Contrary to expectations, salinomycin induced the expression of EMT markers Snail, vimentin, and Zeb-1, decreased expression of E-cadherin, and also induced phosphorylation of Akt and its downstream targets GSK3-β and mTOR. Conclusions These results demonstrate that in HNSCC cancer stem cells, salinomycin can cause cell death and decrease stem cell properties despite activation of both EMT and Akt.
- Published
- 2012
33. Recombinant human erythropoietin promotes the acquisition of a malignant phenotype in head and neck squamous cell carcinoma cell lines in vitro
- Author
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Abhold, Eric, Rahimy, Elham, Wang-Rodriguez, Jessica, Blair, Katherine J, Yu, Michael A, Brumund, Kevin T, Weisman, Robert A, and Ongkeko, Weg M
- Abstract
Abstract Background Recent studies indicate an increase in tumor progression and recurrence in head and neck squamous cell carcinomas (HNSCC) of cancer patients taking recombinant human erythropoietin (rhEpo) for anemia. This study was undertaken to investigate the potential role of rhEpo in invasion, proliferation, and cisplatin-induced cell death in HNSCC cell lines. Methods The following experiments were performed with two HNSCC cell lines, UMSCC-10B and UMSCC-22B. Presence of EpoR in both cell lines was determined by western blot and quantitative PCR. Colorimetric MTS assays and clonogenic assays were used to study the effect of rhEpo at pharmacologically relevant doses on cell proliferation. Matrigel invasion assays were performed in order to determine effects of exogenous rhEpo on invasive abilities. Clonogenic assays were also used to study potential cytoprotective effects of rhEpo against cisplatin. Immunoblotting was done to analyze the effect of rhEpo on Akt phosphorylation. Finally, MTS and TUNEL assays were performed to test our hypothesis that Akt activation by PI3K was involved in rhEpo-mediated cisplatin resistance. Results HNSCC cell lines were shown to express Epo receptor (EpoR). RhEpo increased invasion 1.8-fold in UMSCC-10B and 2.6-fold in UMSCC-22B compared to control. RhEpo at 10 U/ml increased cell proliferation by 41% and 53% in UMSCC-10B and UMSCC-22B, respectively, and colony formation by 1.5-fold and 1.8-fold. UMSCC-10B treated with cisplatin and exposed to rhEpo at 1 and 10 U/ml resulted in a 1.7-fold and 3.0-fold increase in colony number compared to control, respectively. UMSCC-22B treated with cisplatin and rhEpo at 1 or 10 U/ml resulted in ~2.5-fold increase in colony number. A TUNEL assay demonstrated a 30.5% and 76.5% increase in survival in UMSCC-10B and UMSCC-22B cells, respectively, in cisplatin and rhEpo-treated cells compared to cisplatin alone. MTS assay showed similar cytoprotective effects. Western blot revealed increased phosphorylation of Akt upon exposure of HNSCC cell lines to rhEpo. MTS assay and TUNEL analyses implicate Akt as a likely contributor to regulation of rhEpo-mediated cytoprotection. Conclusions The results demonstrate that, in HNSCC cells expressing functional EpoR, rhEpo promotes invasion, cell proliferation, and induces resistance to cisplatin, which may contribute to tumor progression.
- Published
- 2011
34. Abstract LB110: Racial and ethnic disparities associated with the intratumor microbiome in female cancers
- Author
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Uzelac, Matthew, primary, Li, Wei Tse, additional, Chakladar, Jaideep, additional, John, Daniel, additional, and Ongkeko, Weg M., additional
- Published
- 2023
- Full Text
- View/download PDF
35. A comprehensive study of smoking-specific microRNA alterations in head and neck squamous cell carcinoma
- Author
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Krishnan, Aswini R., Zheng, Hao, Kwok, James G., Qu, Yuanhao, Zou, Angela E., Korrapati, Avinaash, Li, Pin Xue, Califano, Joseph A., Hovell, Melbourne F., Wang-Rodriguez, Jessica, and Ongkeko, Weg M.
- Published
- 2017
- Full Text
- View/download PDF
36. Smoking status regulates a novel panel of PIWI-interacting RNAs in head and neck squamous cell carcinoma
- Author
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Krishnan, Aswini R., Korrapati, Avinaash, Zou, Angela E., Qu, Yuanhao, Wang, Xiao Qi, Califano, Joseph A., Wang-Rodriguez, Jessica, Lippman, Scott M., Hovell, Melbourne F., and Ongkeko, Weg M.
- Published
- 2017
- Full Text
- View/download PDF
37. Using machine learning of clinical data to diagnose COVID-19: a systematic review and meta-analysis
- Author
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Li, Wei Tse, Ma, Jiayan, Shende, Neil, Castaneda, Grant, Chakladar, Jaideep, Tsai, Joseph C., Apostol, Lauren, Honda, Christine O., Xu, Jingyue, Wong, Lindsay M., Zhang, Tianyi, Lee, Abby, Gnanasekar, Aditi, Honda, Thomas K., Kuo, Selena Z., Yu, Michael Andrew, Chang, Eric Y., Rajasekaran, Mahadevan “ Raj”, and Ongkeko, Weg M.
- Published
- 2020
- Full Text
- View/download PDF
38. Characterization of tRNA-Derived Fragments in Lung Squamous Cell Carcinoma with Respect to Tobacco Smoke
- Author
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Magesh, Shruti, primary, Gande, Pranava, additional, Yalamarty, Rishabh, additional, John, Daniel, additional, Chakladar, Jaideep, additional, Li, Wei Tse, additional, and Ongkeko, Weg M., additional
- Published
- 2023
- Full Text
- View/download PDF
39. Transcriptomic Analysis Reveals Dysregulation of the Mycobiome and Archaeome and Distinct Oncogenic Characteristics according to Subtype and Gender in Papillary Thyroid Carcinoma
- Author
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John, Daniel, primary, Yalamarty, Rishabh, additional, Barakchi, Armon, additional, Chen, Tianyi, additional, Chakladar, Jaideep, additional, Li, Wei Tse, additional, and Ongkeko, Weg M., additional
- Published
- 2023
- Full Text
- View/download PDF
40. The role of Cdc2 and p53 in cell cycle checkpoints and apoptosis
- Author
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Ongkeko, Weg M.
- Subjects
572 ,Cancer research ,Cell death - Published
- 1998
41. Effects of Human Papilloma Virus E6/E7 Oncoproteins on Genomic Structure in Head and Neck Squamous Cell Carcinoma
- Author
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Uzelac, Matthew, primary, Barakchi, Armon, additional, Beldona, Varsha, additional, John, Daniel, additional, Chakladar, Jaideep, additional, Li, Wei Tse, additional, and Ongkeko, Weg M., additional
- Published
- 2022
- Full Text
- View/download PDF
42. The Intratumor Bacterial and Fungal Microbiome Is Characterized by HPV, Smoking, and Alcohol Consumption in Head and Neck Squamous Cell Carcinoma
- Author
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Chakladar, Jaideep, primary, John, Daniel, additional, Magesh, Shruti, additional, Uzelac, Matthew, additional, Li, Wei Tse, additional, Dereschuk, Kypros, additional, Apostol, Lauren, additional, Brumund, Kevin T., additional, Rodriguez, Jessica-Wang, additional, and Ongkeko, Weg M., additional
- Published
- 2022
- Full Text
- View/download PDF
43. Archaea Microbiome Dysregulated Genes and Pathways as Molecular Targets for Lung Adenocarcinoma and Squamous Cell Carcinoma
- Author
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Uzelac, Matthew, primary, Li, Yuxiang, additional, Chakladar, Jaideep, additional, Li, Wei Tse, additional, and Ongkeko, Weg M., additional
- Published
- 2022
- Full Text
- View/download PDF
44. Abstract 3528: Influence of obesity-associated intra-tumor microbes on exacerbating cancer severity
- Author
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Gnanasekar, Aditi, primary, Shende, Neil, additional, Chakladar, Jaideep, additional, Li, Wei T., additional, Wong, Lindsay M., additional, Karin, Michael, additional, and Ongkeko, Weg M., additional
- Published
- 2022
- Full Text
- View/download PDF
45. Abstract 1337: Pan-cancer analysis of immune-associated genes and pathways dysregulated by tobacco reveals osteopontin as a key mediator of smoking-associated carcinogenesis
- Author
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Chakladar, Jaideep, primary, Shende, Neil, additional, Li, Wei Tse, additional, and Ongkeko, Weg M., additional
- Published
- 2022
- Full Text
- View/download PDF
46. Additional file 2 of Medical student���s perception of the COVID-19 pandemic effect on their education and well-being: a cross-sectional survey in the United States
- Author
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Chakladar, Jaideep, Diomino, Anthony, Li, Wei Tse, Tsai, Joseph C., Krishnan, Aswini R., Zou, Angela E., Kharidia, Khush, Baig, Farhan A., Householder, Sarah, Kuo, Selena Z., Chandrasekar, Shyam, Chang, Eric Y., and Ongkeko, Weg M.
- Subjects
Data_FILES - Abstract
Additional file 2.
- Published
- 2022
- Full Text
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47. Enhancer RNA Profiling in Smoking and HPV Associated HNSCC Reveals Associations to Key Oncogenes
- Author
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Shende, Neil, primary, Xu, Jingyue, additional, Li, Wei Tse, additional, Liu, Jeffrey, additional, Chakladar, Jaideep, additional, Brumund, Kevin T., additional, and Ongkeko, Weg M., additional
- Published
- 2021
- Full Text
- View/download PDF
48. Disparities in COVID-19 Outcomes by Race, Ethnicity, and Socioeconomic Status
- Author
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Magesh, Shruti, primary, John, Daniel, additional, Li, Wei Tse, additional, Li, Yuxiang, additional, Mattingly-app, Aidan, additional, Jain, Sharad, additional, Chang, Eric Y., additional, and Ongkeko, Weg M., additional
- Published
- 2021
- Full Text
- View/download PDF
49. Tobacco Smoke and Electronic Cigarette Vapor Alter Enhancer RNA Expression That Can Regulate the Pathogenesis of Lung Squamous Cell Carcinoma
- Author
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Tsai, Joseph C., primary, Saad, Omar A., additional, Magesh, Shruti, additional, Xu, Jingyue, additional, Lee, Abby C., additional, Li, Wei Tse, additional, Chakladar, Jaideep, additional, Fuster, Mark M., additional, Chang, Eric Y., additional, Wang-Rodriguez, Jessica, additional, and Ongkeko, Weg M., additional
- Published
- 2021
- Full Text
- View/download PDF
50. The Bladder Microbiome Is Associated with Epithelial–Mesenchymal Transition in Muscle Invasive Urothelial Bladder Carcinoma
- Author
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Li, Wei Tse, primary, Iyangar, Anjali S., additional, Reddy, Rohan, additional, Chakladar, Jaideep, additional, Bhargava, Valmik, additional, Sakamoto, Kyoko, additional, Ongkeko, Weg M., additional, and Rajasekaran, Mahadevan, additional
- Published
- 2021
- Full Text
- View/download PDF
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