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Cullin7: a new gene involved in liver carcinogenesis related to metabolic syndrome
  1. Valerie Paradis1,2,
  2. Miguel Albuquerque1,
  3. Mouniya Mebarki2,
  4. Lucie Hernandez3,
  5. Stephane Zalinski4,
  6. Samuel Quentin3,
  7. Jacques Belghiti4,
  8. Jean Soulier3,
  9. Pierre Bedossa1,2
  1. 1Pathology Department, Beaujon Hospital, Clichy, France
  2. 2INSERM U773-CRB3, Diderot-Paris 7 University, Paris, France
  3. 3Centre Hayem, University Institute of Hematology, Saint Louis Hospital, Paris, France
  4. 4Hepatobiliary Surgery Department, Beaujon Hospital, Clichy, France
  1. Correspondence to Professor Valerie Paradis, Pathology Department, Beaujon Hospital, 100 boulevard du Général Leclerc, Clichy 92118, France; vparadis{at}teaser.fr

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.

  • CANCER GENETICS
  • NONALCOHOLIC STEATOHEPATITIS
  • CELL PROLIFERATION
  • CIRRHOSIS
  • HEPATOCELLULAR CARCINOMA

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