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ARHI, as a novel suppressor of cell growth and downregulated in human hepatocellular carcinoma, could contribute to hepatocarcinogenesis
Author(s) -
Huang Jian,
Lin Yun,
Li Lihua,
Qing Deng,
Teng XiaoMei,
Zhang YunLi,
Hu Xin,
Hu Yuanjie,
Yang Pengyuan,
Han ZeGuang
Publication year - 2009
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.20461
Subject(s) - biology , hccs , cancer research , gene silencing , tumor suppressor gene , liver cancer , cell growth , epigenetics , cancer , hepatocellular carcinoma , microbiology and biotechnology , dna methylation , carcinogenesis , cell , cancer cell , rna interference , suppressor , gene expression , gene , genetics , rna
The identification of cancer genes differentially expressed in hepatocellular carcinoma (HCC) plays an important role in understanding the molecular mechanisms of hepatocarcinogenesis. Here, ARHI gene expression was analyzed by real‐time RT‐PCR and it was significantly downregulated in 33 of the 42 (78.6%, more than two folds) HCC specimens compared with adjacent noncancerous livers ( P < 0.01). In addition, ARHI expression was reduced in some HCC samples at protein level confirmed by immunohistochemistry. Furthermore, our data suggested that the overexpression of ARHI can significantly inhibit cell growth and colony formation of Hep3B cells ( P < 0.01), whilst silencing endogenous ARHI gene by RNAi could promote cell growth of Huh‐7 and Focus. LOH of microsatellite markers D1S2806 and D1S2803 was only found in 2.4% (1 of 42 HCCs) of HCC cases. The expression of ARHI was obviously re‐expressed in some HCC cells, Bel‐7402, Bel‐7405, QGY‐7703 and Hep3B, by a demethylation agent, 5‐aza‐2′‐deoxycytidine (DAC). DNA hypermethylation within ARHI promoter was identified in 47.1% of HCC specimens without ARHI expression. Our current observations provide evidences that ARHI downregulated in HCCs could play a role in liver cancer via acting as a tumor suppressor gene, which mainly was triggered by the epigenetic events in HCC specimens. © 2008 Wiley‐Liss, Inc.