Overexpression of the two nucleotide excision repair genes ERCC1 and XPC in human hepatocellular carcinoma.

Abstract:

BACKGROUND/AIMS:Little is known about the nucleotide excision repair (NER) pathway in the resistance of human hepatocellular carcinoma (HCC) to chemotherapeutics. We investigated expression of several NER genes in human HCC and matching non-tumor tissue (NT) and in normal liver. METHODS:Expression of CSA, CSB, XPC, hHR23B, XPA, XPB, ERCC1 and p53 genes was analyzed by quantitative RT-PCR and immunoblotting in 26 HCC and 9 normal livers. RESULTS:The seven NER genes and p53 were frequently overexpressed in HCC compared to matched NT. XPA, XPC, hHR23B and ERCC1 mRNA levels were significantly increased (p<0.05) in HCC arising in cirrhotic livers compared to non fibrotic tissue. Moreover, expression of ERCC1, XPA and XPC mRNA was significantly augmented in HCC, even more in tumors arising in cirrhotic liver. ERCC1, XPC ad XPA mRNA levels were highly correlated in NT and HCC. XPC and ERCC1 protein levels were also increased in HCC. CONCLUSIONS:Our findings strongly suggest that overexpression of two key genes involved in the early steps of the NER process, ERCC1 and XPC, is associated with liver fibrogenesis and cancer and could be related to the well recognized resistance of HCC to chemotherapeutics.

journal_name

J Hepatol

journal_title

Journal of hepatology

authors

Fautrel A,Andrieux L,Musso O,Boudjema K,Guillouzo A,Langouët S

doi

10.1016/j.jhep.2005.02.020

subject

Has Abstract

pub_date

2005-08-01 00:00:00

pages

288-93

issue

2

eissn

0168-8278

issn

1600-0641

pii

S0168-8278(05)00248-5

journal_volume

43

pub_type

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