Cullin7: a new gene involved in liver carcinogenesis related to metabolic syndrome. Issue 6 (1st September 2012)

• Record Type: Journal Article
• Authors: Paradis, Valerie; Albuquerque, Miguel; Mebarki, Mouniya; Hernandez, Lucie; Zalinski, Stephane; Quentin, Samuel; Belghiti, Jacques; Soulier, Jean; Bedossa, Pierre
• Is Part Of: Gut. Volume 62:Issue 6(2013)
• Page Start: 911
• Page End: 919
• Publication Date: 2012-09-01
• Subjects: CANCER GENETICS -- NONALCOHOLIC STEATOHEPATITIS -- CELL PROLIFERATION -- CIRRHOSIS -- HEPATOCELLULAR CARCINOMA; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gutjnl-2012-302091
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : Background: Metabolic syndrome (MS) is an emerging risk factor in hepatocellular carcinoma (HCC). HCC related to MS may occur either in advanced fibrosis or before the development of cirrhosis, suggesting involvement of different molecular pathways according to the features of background liver. Objective: To investigate genomic aberrations in HCC related to MS in order to identify new target genes involved in liver carcinogenesis. Methods: Chromosomal aberrations of HCC obtained from 20 patients with MS (HCC/MS) were studied by comparative genomic hybridisation and compared with HCC related to hepatitis C virus (HCV) infection (HCC/HCV, n=10) and, within the group of HCC with MS, according to the condition of the background liver (presence or absence of significant fibrosis). Results: Among the most frequent chromosomal alterations observed in HCC, 6p21.1 amplification had a higher incidence in HCC/MS than in HCC/HCV (60% vs 20%, p<0.01). Advanced fibrosis/cirrhosis in the peritumoral liver was the only clinicopathological factor associated with the 6p21.1 amplicon in HCC/MS. Increased expression of cullin7 (CUL7), a gene located at the 6p21.1 locus, was demonstrated in HCC with the 6p21.1 amplicon, in parallel with a decrease in cyclin D1 expression. CUL7 downregulation using siRNA transfection in hepatoma cell lines induced significant cyclin D1 expression (by promoting its degradation), decreased cell proliferation and increased apoptosis. Conclusions: This study demonstrates specific genomic alterations in HCC/MS and points to CUL7 as a novel gene potentially involved in liver carcinogenesis associated with MS, the amplification of which might influence cell proliferation.