Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Apr 29;20(4):1147-1151.
doi: 10.31557/APJCP.2019.20.4.1147.

Study on JV Virus in Patients with Colon Cancer Type Adenocarcinoma

Affiliations

Study on JV Virus in Patients with Colon Cancer Type Adenocarcinoma

Azadeh Haghi Navand et al. Asian Pac J Cancer Prev. .

Abstract

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.

Keywords: JC virus; colorectal adenocarcinoma; polymerase chine reaction.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Results of JCV PCR in Patients with CRC. Line 1, Negative sample; Line 2-6, Positive samples; NC, Negative Control; PC, Positive sample; Molecular Marker (100bp size)
Figure 2
Figure 2
Phylogeny Tree was Constructed by Maximum Likelihood Method for JCV Vp1/T-Ag Junction Region of the Isolated JC virus Genomes with Accession Number KX230698- KX230703 Labeled by the Black Solid Circle. TThey were compared with different JCV Vp1/TAg junction isolated from different regions of the world with accession numbers retrieved from Gen Bank

Similar articles

Cited by

References

    1. Bouvard V, Baan RA, Grosse Y, et al. Carcinogenicity of malaria and of some polyomaviruses. Lancet Oncol. 2012;13:339–40. - PubMed
    1. Castellarin M, Warren RL, Freeman JD, et al. Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma. Genome Res. 2012;22:299–306. - PMC - PubMed
    1. Caiqin H, Ying H, Junwei S, et al. Detection and analysis of variants of JC polyomavirus in urine samples from HIV-1-infected patients in China’s Zhejiang Province. Int Med Res. 2018;46:1024–32. - PMC - PubMed
    1. Coelho TR, Gaspar R, Figueiredo P, et al. Human JC polyomavirus in normal colorectal mucosa, hyperplastic polyps, sporadic adenomas, and adenocarcinomas in Portugal. J Med Virol. 2013;85:2119–27. - PubMed
    1. Coelho TR, Almeida L, Lazo PA, et al. JC virus in the pathogenesis of colorectal cancer, an etiological agent or another component in a multistep process? Virol J. 2010;7:42. - PMC - PubMed

MeSH terms