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Oncogenic role of JC virus in lung cancer
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990319)83:3<152::aid-ajmg3>3.0.co;2-oopenalex-snapshot
JC virus and its possible role in oncogenesis
inferredcites →https://doi.org/10.1002/(sici)1097-0142(19980615)82:12<2334::aid-cncr6>3.0.co;2-sopenalex-snapshot
Epstein-barr virus-associated nonsmall cell lung carcinoma
inferredcites →https://doi.org/10.1002/ana.410360421openalex-snapshot
In situ polymerase chain reaction demonstration of JC virus in progressive multifocal leukoencephalopathy, including an index case
inferredcites →https://doi.org/10.1002/cncr.20806openalex-snapshot
Detection of JC virus DNA sequences and expression of viral T antigen and agnoprotein in esophageal carcinoma
inferredcites →https://doi.org/10.1002/cncr.22028openalex-snapshot
Oncogenic T‐antigen of JC virus is present frequently in human gastric cancers
inferredcites →https://doi.org/10.1002/jmv.1890420208openalex-snapshot
Detection by PCR of human polyomaviruses BK and JC in immunocompromised individuals and partial sequencing of control regions
inferredcites →https://doi.org/10.1002/pros.10157openalex-snapshot
Detection of human polyomaviruses and papillomaviruses in prostatic tissue reveals the prostate as a habitat for multiple viral infections
inferredcites →https://doi.org/10.1007/978-3-642-82982-6openalex-snapshot
TNM Classification of Malignant Tumours
inferredcites →https://doi.org/10.1007/s00428-005-0014-3openalex-snapshot
Detection of JC virus DNA sequences in colorectal cancers in Japan
inferredcites →https://doi.org/10.1007/s10350-004-0737-2openalex-snapshot
Assessment of JC Polyoma Virus in Colon Neoplasms
inferredcites →https://doi.org/10.1016/j.ejca.2005.08.019openalex-snapshot
Expression of JC virus regulatory proteins in human cancer: Potential mechanisms for tumourigenesis
inferredcites →https://doi.org/10.1016/j.virol.2004.03.025openalex-snapshot
Polyomaviruses and human cancer: molecular mechanisms underlying patterns of tumorigenesis
inferredcites →https://doi.org/10.1016/s0002-9440(10)63132-xopenalex-snapshot
Differential Distribution of the JC Virus Receptor-Type Sialic Acid in Normal Human Tissues
inferredcites →https://doi.org/10.1016/s0025-6196(12)60701-0openalex-snapshot
Nonradioactive In Situ Hybridization in Progressive Multifocal Leukoencephalopathy
inferredcites →https://doi.org/10.1038/modpathol.3800165openalex-snapshot
Improved 1-h rapid immunostaining method using intermittent microwave irradiation: practicability based on 5 years application in Toyama Medical and Pharmaceutical University Hospital
inferredcites →https://doi.org/10.1038/sj.onc.1203849openalex-snapshot
Pituitary neoplasia induced by expression of human neurotropic polyomavirus, JCV, early genome in transgenic mice
inferredcites →https://doi.org/10.1038/sj.onc.1206559openalex-snapshot
Human neurotropic polyomavirus, JCV, and its role in carcinogenesis
inferredcites →https://doi.org/10.1038/sj.onc.1206959openalex-snapshot
Viruses and cancer: lessons from the human polyomavirus, JCV
inferredcites →https://doi.org/10.1038/sj.onc.1207018openalex-snapshot
Interaction between JCV large T-antigen and β-catenin
inferredcites →https://doi.org/10.1053/gast.2000.19269openalex-snapshot
JC virus DNA sequences are frequently present in the human upper and lower gastrointestinal tract
inferredcites →https://doi.org/10.1073/pnas.93.24.14112openalex-snapshot
Activation of the JC virus Tat-responsive transcriptional control element by association of the Tat protein of human immunodeficiency virus 1 with cellular protein Purα
inferredcites →https://doi.org/10.1097/00000478-199810000-00016openalex-snapshot
TNM Classification of Malignant Tumors
inferredcites →https://doi.org/10.1111/j.1349-7006.2006.00354.xopenalex-snapshot
High JC virus load in gastric cancer and adjacent non‐cancerous mucosa
inferredcites →https://doi.org/10.1111/j.1440-1827.2006.01964.xopenalex-snapshot
Human papillomavirus localization in cervical adenocarcinoma and adenosquamous carcinoma using in situ polymerase chain reaction: Review of the literature of human papillomavirus detection in these carcinomas
inferredcites →https://doi.org/10.1128/jvi.51.2.458-469.1984openalex-snapshot
Human polyomavirus JC virus genome
inferredcites →https://doi.org/10.1128/jvi.64.3.1353-1356.1990openalex-snapshot
Large T antigens of many polyomaviruses are able to form complexes with the retinoblastoma protein
inferredcites →https://doi.org/10.1128/jvi.72.12.9918-9923.1998openalex-snapshot
Detection of JC Virus DNA in Human Tonsil Tissue: Evidence for Site of Initial Viral Infection
inferredcites →https://doi.org/10.1128/jvi.75.4.1996-2001.2001openalex-snapshot
Mad-1 Is the Exclusive JC Virus Strain Present in the Human Colon, and Its Transcriptional Control Region Has a Deleted 98-Base-Pair Sequence in Colon Cancer Tissues
inferredcites →https://doi.org/10.1128/jvi.78.7.3462-3469.2004openalex-snapshot
Primary Central Nervous System Lymphoma Expressing the Human Neurotropic Polyomavirus, JC Virus, Genome
inferredcites →https://doi.org/10.1159/000150537openalex-snapshot
Progressive Multifocal Leukoencephalopathy: Molecular Biology, Pathogenesis and Clinical Impact
inferredcites →https://doi.org/10.1200/jco.2005.10.462openalex-snapshot
Epidemiology of Lung Cancer: Looking to the Future
inferredcites →https://doi.org/10.3748/wjg.v9.i7.1415openalex-snapshot
Expression of Fas ligand and Caspase-3 contributes to formation of immune escape in gastric cancer
inferredcites →https://doi.org/10.5858/2005-129-69-kautpiopenalex-snapshot
Kidney and Urinary Tract Polyomavirus Infection and Distribution: Molecular Biology Investigation of 10 Consecutive Autopsies
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4089618openalex-extracted
The Oncogenic Roles of John Cunningham Polyomavirus T Antigen in Cervical Cancer
inferred← citeshttps://doi.org/10.1002/jcb.22525openalex-snapshot
EXPRESSION OF CONCERN: Cross‐talk between T‐Ag presence and pRb family and p53/p73 signaling in mouse and human medulloblastoma
inferred← citeshttps://doi.org/10.1002/jmv.21296openalex-snapshot
Prevalence and genotype identification of human JC virus in colon cancer in Taiwan
inferred← citeshttps://doi.org/10.1002/jmv.21303openalex-snapshot
Identification of the novel KI polyomavirus in the respiratory tract of an Italian patient
inferred← citeshttps://doi.org/10.1002/jmv.21417openalex-snapshot
Identification of the novel KI Polyomavirus in paranasal and lung tissues
inferred← citeshttps://doi.org/10.1002/jmv.22240openalex-snapshot
The high incidence of JC virus infection in urothelial carcinoma tissue in Taiwan
inferred← citeshttps://doi.org/10.1007/978-1-4020-8833-9_22openalex-snapshot
The role of the polyomavirus, JC virus, in the pathogenesis of colorectal cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-29716-3_14openalex-snapshot
Evolution, Infection, and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-319-46248-6_6openalex-snapshot
Carcinogenic Toxicity of Cigarette Smoke: A Computational Enzymatic Interaction and DNA Repair Pathways
inferred← citeshttps://doi.org/10.1007/s00401-010-0694-xopenalex-snapshot
Progressive multifocal leukoencephalopathy and promyelocytic leukemia nuclear bodies: a review of clinical, neuropathological, and virological aspects of JC virus-induced demyelinating disease
inferred← citeshttps://doi.org/10.1007/s00428-007-0534-0openalex-snapshot
High JC virus load in tongue carcinomas may be a risk factor for tongue tumorigenesis
inferred← citeshttps://doi.org/10.1007/s00705-014-2230-0openalex-snapshot
Prevalence of JC polyomavirus large T antigen sequences among Iranian patients with central nervous system tumors
inferred← citeshttps://doi.org/10.1007/s00705-021-05268-8openalex-snapshot
Association between viral infection other than human papillomavirus and risk of esophageal carcinoma: a comprehensive meta-analysis of epidemiological studies
inferred← citeshttps://doi.org/10.1007/s10096-013-2010-xopenalex-snapshot
Detection of human JCPyV and BKPyV in diffuse large B-cell lymphoma of the GI tract
inferred← citeshttps://doi.org/10.1007/s10096-018-3204-zopenalex-snapshot
Smoking is not associated with higher prevalence of JC virus in MS patients
inferred← citeshttps://doi.org/10.1007/s10549-011-1876-5openalex-snapshot
Investigation of human JC and BK polyomaviruses in breast carcinomas
inferred← citeshttps://doi.org/10.1007/s10555-011-9342-8openalex-snapshot
A new hypothesis for the cancer mechanism
inferred← citeshttps://doi.org/10.1007/s11248-023-00352-yopenalex-snapshot
The potential oncogenic effect of tissue-specific expression of JC polyoma T antigen in digestive epithelial cells
inferred← citeshttps://doi.org/10.1007/s11284-011-0874-8openalex-snapshot
Evolution of virulence, environmental change, and the threat posed by emerging and chronic diseases
inferred← citeshttps://doi.org/10.1007/s13402-025-01103-3openalex-snapshot
The emerging role of microbiota in lung cancer: a new perspective on lung cancer development and treatment
inferred← citeshttps://doi.org/10.1016/b978-0-12-818619-0.00092-7openalex-snapshot
Viruses, cell transformation, and cancer
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155521openalex-snapshot
Association of polyomavirus infection with lung cancer: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.semcancer.2009.02.013openalex-snapshot
JC Virus: An oncogenic virus in animals and humans?
inferred← citeshttps://doi.org/10.1016/j.transproceed.2010.02.068openalex-snapshot
High Incidence of Malignancy in Polyomavirus-Associated Nephropathy in Renal Transplant Recipients
inferred← citeshttps://doi.org/10.1038/bjc.2016.285openalex-snapshot
Serum biomarkers of polyomavirus infection and risk of lung cancer in never smokers
inferred← citeshttps://doi.org/10.1038/gt.2010.50openalex-snapshot
Efficient gene transfer using the human JC virus-like particle that inhibits human colon adenocarcinoma growth in a nude mouse model
inferred← citeshttps://doi.org/10.1080/0284186x.2019.1657588openalex-snapshot
Analysis of human papillomaviruses and human polyomaviruses in lung cancer from Swedish never-smokers
inferred← citeshttps://doi.org/10.1080/1040841x.2024.2324864openalex-snapshot
The implication of microbiome in lungs cancer: mechanisms and strategies of cancer growth, diagnosis and therapy
inferred← citeshttps://doi.org/10.1093/mutage/gev004openalex-snapshot
Human JC virus small tumour antigen inhibits nucleotide excision repair and sensitises cells to DNA-damaging agents
inferred← citeshttps://doi.org/10.1093/nar/gkad199openalex-snapshot
Unmasking the tissue-resident eukaryotic DNA virome in humans
inferred← citeshttps://doi.org/10.1097/nen.0b013e318180e631openalex-snapshot
Potential Mechanisms of the Human Polyomavirus JC in Neural Oncogenesis
inferred← citeshttps://doi.org/10.1097/pas.0b013e3181ba7b73openalex-snapshot
Merkel Cell Polyomavirus
inferred← citeshttps://doi.org/10.1099/mgen.0.001509openalex-snapshot
Lung microbiome dynamics in health and lung cancer
inferred← citeshttps://doi.org/10.1109/tcbb.2012.65openalex-snapshot
Detecting Phenotype-Specific Interactions between Biological Processes from Microarray Data and Annotations
inferred← citeshttps://doi.org/10.1111/1759-7714.12030openalex-snapshot
Human papillomavirus and non‐small cell lung cancer
inferred← citeshttps://doi.org/10.1111/j.1610-0387.2008.06810.xopenalex-snapshot
Human polyomaviruses and cancer: expanding repertoire
inferred← citeshttps://doi.org/10.1142/9781848163140_0017openalex-snapshot
Potential for Immunotherapy in Merkel Cell Carcinoma
inferred← citeshttps://doi.org/10.1155/2011/635379openalex-snapshot
NNK-Induced Lung Tumors: A Review of Animal Model
inferred← citeshttps://doi.org/10.1158/0008-5472.can-09-2719openalex-snapshot
The Bisecting GlcNAc on N -Glycans Inhibits Growth Factor Signaling and Retards Mammary Tumor Progression
inferred← citeshttps://doi.org/10.1158/1538-7445.am2011-275openalex-snapshot
Abstract 275: Burkitt lymphoma cells express GLI1 but are not responsive to Hedgehog signaling
inferred← citeshttps://doi.org/10.1172/jci.insight.85562openalex-snapshot
Survey for human polyomaviruses in cancer
inferred← citeshttps://doi.org/10.1186/1471-2334-9-28openalex-snapshot
Mapping the history and current situation of research on John Cunningham virus – a bibliometric analysis
inferred← citeshttps://doi.org/10.1371/journal.pone.0106257openalex-snapshot
Activation of c-Myc and Cyclin D1 by JCV T-Antigen and β-Catenin in Colon Cancer
inferred← citeshttps://doi.org/10.1371/journal.pone.0157865openalex-snapshot
Gene Therapy for Human Lung Adenocarcinoma Using a Suicide Gene Driven by a Lung-Specific Promoter Delivered by JC Virus-Like Particles
inferred← citeshttps://doi.org/10.1517/14712598.2011.583914openalex-snapshot
Human JC virus-like particles as a gene delivery vector
inferred← citeshttps://doi.org/10.18632/oncotarget.3507openalex-snapshot
The oncogenic role of JC virus T antigen in lens tumors without cell specificity of alternative splicing of its intron
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1818052/v1openalex-snapshot
The oncogenic roles of JC polyomavirus T antigen in cervical cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1927120/v1openalex-snapshot
The oncogenic roles of John Cunningham virus T antigen in digestive epithelial cells with tissue specificity
inferred← citeshttps://doi.org/10.2147/ott.s263976openalex-snapshot
Possible Oncogenic Viruses Associated with Lung Cancer
inferred← citeshttps://doi.org/10.21873/anticanres.11699openalex-snapshot
JC Virus and Lung Adenocarcinoma: Fact or Myth?
inferred← citeshttps://doi.org/10.3389/fmolb.2021.687444openalex-snapshot
The Oncogenic Roles of JC Virus T Antigen in Breast Carcinogenesis
inferred← citeshttps://doi.org/10.3389/fonc.2022.744886openalex-snapshot
The Oncogenic Effects, Pathways, and Target Molecules of JC Polyoma Virus T Antigen in Cancer Cells
inferred← citeshttps://doi.org/10.3389/fonc.2022.976577openalex-snapshot
The oncogenic roles of JC polyomavirus in cancer
inferred← citeshttps://doi.org/10.3390/biology11121691openalex-snapshot
High-Risk Human Papillomavirus Infection in Lung Cancer: Mechanisms and Perspectives
inferred← citeshttps://doi.org/10.3390/ijms22158332openalex-snapshot
Dual Nature of Relationship between Mycobacteria and Cancer
inferred← citeshttps://doi.org/10.3390/pathogens11020132openalex-snapshot
Epstein–Barr Virus Infection in Lung Cancer: Insights and Perspectives
inferred← citeshttps://doi.org/10.3390/v15102112openalex-snapshot
Polyomavirus Wakes Up and Chooses Neurovirulence
inferred← citeshttps://doi.org/10.36348/sjbr.2022.v07i02.002openalex-snapshot
An Overview on Viral Origin of Cancer in Human
inferred← citeshttps://doi.org/10.3892/ol.2012.627openalex-snapshot
JC virus existence in Chinese gastrointestinal carcinomas
inferred← citeshttps://doi.org/10.3892/ol.2016.5012openalex-snapshot
Differential expression of viral agents in lymphoma tissues of patients with ABC diffuse large B-cell lymphoma from high and low endemic infectious disease regions
inferred← citeshttps://doi.org/10.3892/or.2013.2782openalex-snapshot
Pulmonary tumors associated with the JC virus T-antigen in a transgenic mouse model
inferred← citeshttps://doi.org/10.48175/ijarsct-15967openalex-snapshot
A Review on Lung Cancer with Emphasis on Current Treatment
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