Evidence map›Paper›PMID 40888995›Full record

ArticleJournal of the Egyptian National Cancer Institute2025

Nested PCR detection of JC polyomavirus large T-antigen in prostate cancer tissues: a case-control analysis in a Sudanese population.

Maria Ahmed Mohamed Higair, Babbiker Mohammed Taher Gorish, Sana Eltahir Abdallah

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Article in Journal of the Egyptian National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Maria Ahmed Mohamed HigairInstitute of Medical Research, Al-Neelain University, Sudan, Khartoum, Sudan.
Babbiker Mohammed Taher GorishDepartment of Microbiology, College of Medical Laboratory Science, Omdurman Islamic University, Omdurman, Sudan. qorish456@gmail.com.
Sana Eltahir AbdallahDepartment of Pathology, Faculty of Medicine,, Al-Neelain University, Khartoum, Sudan. sanaeltahir.se@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe potential involvement of JC polyomavirus (JCPyV) in prostate cancer (PCa) remains a subject of debate, as existing in vitro studies have produced conflicting results. Understanding the viral oncogenic mechanisms underlying prostate cancer could offer valuable insights into its etiology. This study aimed to explore the association between JCPyV infection and prostate cancer by detecting the viral large T-antigen gene in prostate tissue specimens.

methodsA case-control study was conducted from February 2022 to March 2023, including 100 participants: 50 diagnosed with prostate cancer (cases) and 50 with benign prostatic hyperplasia (BPH) as controls. Formalin-fixed paraffin-embedded (FFPE) prostate tissue samples were collected from all participants. Nested polymerase chain reaction (PCR) was employed to detect JCPyV large T-antigen DNA using specific primers. Demographic and clinical data were obtained via a structured questionnaire. Statistical analysis was carried out using SPSS version 20, and associations between JCPyV presence and prostate cancer were analyzed using logistic regression.

resultsThe mean age of the prostate cancer group was 67.5 ± 10.9 years, compared to 70.9 ± 8.9 years in the control group. JCPyV large T-antigen DNA was detected in 29 out of 50 (58%) prostate cancer cases, compared to 19 out of 50 (38%) controls (P = 0.045; odds ratio = 1.45; 95% confidence interval: 1.011 to 5.019). Within the prostate cancer group, patients testing positive for the JCPyV T-antigen had a mean age of 73.3 ± 8.7 years, significantly higher than T-antigen-negative patients, whose mean age was 67.0 ± 8.3 years (P = 0.029).

conclusionThe prevalence of JCPyV large T-antigen gene was significantly higher in prostate cancer patients than in individuals with benign prostatic hyperplasia. These findings suggest that JCPyV infection may be linked to an increased risk of prostate cancer, reinforcing prior studies that imply a potential oncogenic role for the virus in prostate carcinogenesis. Further investigations are necessary to elucidate the molecular mechanisms driving this association and its potential clinical implications.

Indexed as

Antigens, Viral, TumorJC VirusPolyomavirus InfectionsProstatic NeoplasmsTumor Virus InfectionsAgedCase-Control StudiesDNA, ViralHumansMaleMiddle AgedPolymerase Chain ReactionProstateProstatic HyperplasiaSudanAntigens, Viral, TumorDNA, ViralBenign prostate hyperplasiaJC polyomavirusLarge T antigenProstate cancer

Identifiers

PMID40888995
PMCPMC13313401

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.