Assessment and biological significance of JC polyomavirus in colorectal cancer in Tunisia.
Détails
ID Serval
serval:BIB_A69F11BBCF66
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Assessment and biological significance of JC polyomavirus in colorectal cancer in Tunisia.
Périodique
Journal of B.U.ON.
ISSN
1107-0625 (Print)
ISSN-L
1107-0625
Statut éditorial
Publié
Date de publication
2015
Peer-reviewed
Oui
Volume
20
Numéro
3
Pages
762-769
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
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.
Mots-clé
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
Web of science
Création de la notice
17/10/2023 7:58
Dernière modification de la notice
20/10/2023 6:10