Study on JV Virus in Patients with Colon Cancer Type Adenocarcinoma
JC virus
colorectal adenocarcinoma
polymerase chine reaction
Journal
Asian Pacific journal of cancer prevention : APJCP
ISSN: 2476-762X
Titre abrégé: Asian Pac J Cancer Prev
Pays: Thailand
ID NLM: 101130625
Informations de publication
Date de publication:
29 Apr 2019
29 Apr 2019
Historique:
entrez:
30
4
2019
pubmed:
30
4
2019
medline:
7
9
2019
Statut:
epublish
Résumé
Colorectal cancer is the most repetitious malignancies with high mortality worldwide. JC virus (JCV) is ubiquitous
Polyomavirus, with seroprevalence rates ranging from 70% to 90% in adult population. Recently the role of JCV have
been reported in many malignant tumors worldwide. The association of JCV was reported in patients with colon and
rectum cancers. Thus this study was conducted to evaluate the association of JCV DNA in patients with colon cancer
type Adenocarcinoma. Material and Methods: A total of 120 formalin-fixed paraffin-embedded tissue blocks samples
were collected including 20/40(50%) males, 20/40(50%) females patients with Colorectal Cancer(CRC), and 80 (50%
males, 50% females) patients with benign tumor as a control. DNA was extracted for all the samples. Nested PCR was
carried out for detection of Vp1/T-Ag junction genome in JCV genome by Nested-PCR assay. Randomly, PCR products
of 6 samples were sequenced to analysis the partial JCV DNA. The phylogeny tree was constructed to determine
homology identity with other JCV. Results: 4/40(10%) samples of test group and 10/80 (12.5%) of control samples
were positive for JCV DNA (P= 0.69). Out of 4 samples positive for JC DNA, 3(7.5%) were males and 1(2.4%) female
(P=0.29). The frequency of JCV DNA in age group> 50 years was 4/32(10%), while in age group <50 years was 0/8
(0%) (p= 0.29). Conclusion: prevalence of JCV DNA was among 10% patients with CRC and 12.5% benign tumors
(p=0.69). The distribution of JCV DNA was among 7.5% male and 2.5% female (p= 0.29). The frequency of JCV
DNA was among 10% cases of age group >50 years and 0% of age group <50 years (P= 0.29). The subsequent T-Ag
protein expression might explain the increased risk of colorectal cancer and requires further investigation.
Identifiants
pubmed: 31030488
doi: 10.31557/APJCP.2019.20.4.1147
pmc: PMC6948910
Substances chimiques
DNA, Viral
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1147-1151Informations de copyright
Creative Commons Attribution License
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