Assessment and biological significance of JC polyomavirus in colorectal cancer in Tunisia.
Details
Serval ID
serval:BIB_A69F11BBCF66
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Assessment and biological significance of JC polyomavirus in colorectal cancer in Tunisia.
Journal
Journal of B.U.ON.
ISSN
1107-0625 (Print)
ISSN-L
1107-0625
Publication state
Published
Issued date
2015
Peer-reviewed
Oui
Volume
20
Number
3
Pages
762-769
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Abstract
Several reports have indicated the presence of JC polyomavirus (JCV) in many human tumors, including colorectal cancers (CRCs). The presence of JCV infection in CRC patients has not been investigated in African countries.
We examined the prevalence and the biological significance of JCV in Tunisian CRC patients. The presence of JCV was assessed by polymerase chain reaction (PCR) in a series of 105 CRCs and 89 paired non-tumor colonic mucosa samples from Tunisian patients. Results were correlated with the clinicopathological features and immunohistochemical expression of β-catenin, p53, and the proliferation marker Ki-67.
JCV DNA was detected in 58.1% (61/105) of CRC and in only 14.6% (13/89) of paired non tumor colonic mucosa samples (p=0.03). The presence of JCV was significantly correlated with tumor differentiation (p=0.03). Moreover, JCV presence was significantly correlated with nuclear accumulation of β-catenin (p=0.008) and p53 accumulation (p=0.0001). Multivariate logistic regression analysis showed that tumor differentiation, β-catenin and p53 accumulation were independent parameters significantly associated with the presence of JCV in CRC (p=0.04; p=0.05; p=0.001, respectively).
We support a role of JCV in colorectal carcinogenesis in Tunisian patients, especially of well differentiated morphology.
We examined the prevalence and the biological significance of JCV in Tunisian CRC patients. The presence of JCV was assessed by polymerase chain reaction (PCR) in a series of 105 CRCs and 89 paired non-tumor colonic mucosa samples from Tunisian patients. Results were correlated with the clinicopathological features and immunohistochemical expression of β-catenin, p53, and the proliferation marker Ki-67.
JCV DNA was detected in 58.1% (61/105) of CRC and in only 14.6% (13/89) of paired non tumor colonic mucosa samples (p=0.03). The presence of JCV was significantly correlated with tumor differentiation (p=0.03). Moreover, JCV presence was significantly correlated with nuclear accumulation of β-catenin (p=0.008) and p53 accumulation (p=0.0001). Multivariate logistic regression analysis showed that tumor differentiation, β-catenin and p53 accumulation were independent parameters significantly associated with the presence of JCV in CRC (p=0.04; p=0.05; p=0.001, respectively).
We support a role of JCV in colorectal carcinogenesis in Tunisian patients, especially of well differentiated morphology.
Keywords
Adenocarcinoma/chemistry, Adenocarcinoma/epidemiology, Adenocarcinoma/pathology, Adenocarcinoma/virology, Adenocarcinoma, Mucinous/chemistry, Adenocarcinoma, Mucinous/epidemiology, Adenocarcinoma, Mucinous/pathology, Adenocarcinoma, Mucinous/virology, Biomarkers, Tumor/analysis, Case-Control Studies, Cell Differentiation, Colorectal Neoplasms/chemistry, Colorectal Neoplasms/epidemiology, Colorectal Neoplasms/pathology, Colorectal Neoplasms/virology, DNA, Viral/isolation & purification, Female, Humans, Immunohistochemistry, JC Virus/genetics, JC Virus/isolation & purification, Logistic Models, Male, Middle Aged, Multivariate Analysis, Polymerase Chain Reaction, Polyomavirus Infections/epidemiology, Polyomavirus Infections/metabolism, Polyomavirus Infections/pathology, Polyomavirus Infections/virology, Prevalence, Tumor Suppressor Protein p53/analysis, Tumor Virus Infections/epidemiology, Tumor Virus Infections/metabolism, Tumor Virus Infections/pathology, Tumor Virus Infections/virology, Tunisia/epidemiology, beta Catenin/analysis
Pubmed
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Create date
17/10/2023 7:58
Last modification date
20/10/2023 6:10