Lack of mitochondrial DNA enhances growth of hepatocellular carcinoma in vitro and in vivo

被引:12
|
作者
Haque, Anwarul
Nishikawa, Manabu [1 ]
Qian, Wei
Mashimo, Masayuki
Hirose, Masaki
Nishiguchi, Shuhei
Inoue, Masayasu
机构
[1] Osaka City Univ, Sch Med, Dept Biochem & Mol Pathol, Osaka 5458585, Japan
[2] Hyogo Med Univ, Dept Internal Med, Div Hepatobiliary & Pancreat Dis, Hyogo 6638131, Japan
基金
日本科学技术振兴机构; 美国国家卫生研究院;
关键词
hepatocellular carcinoma; growth; mitochondria; mitochondrial DNA; mutation; rho(0); oxidative stress;
D O I
10.1016/j.hepres.2006.07.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To elucidate the role of mitochondrial DNA (mtDNA) in determination of growth of hepatocellular carcinoma, we examined wild-type Hepa1-6 cells and their rho(0) cells with depleted mtDNA in vitro and in vivo. Cultured rho(0) cells grew more rapidly than did wild-type cells. Production of reactive oxygen species (ROS) was higher in wild-type cells than in rho(0) cells. Hypoxia inhibited the growth of wild-type cells more markedly than that of rho(0) cells. Resistance to mitochondrial respiratory inhibitor-induced cell death was stronger in rho(0) cells than in wild-type cells. rho(0) cells subcutaneously inoculated in the hind thigh of mice grew more rapidly and formed larger solid tumors. These findings indicate that lack of mtDNA increases growth of hepatocellular carcinoma by decreasing ROS production and increasing resistance to mitochondrial respiratory inhibition. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:209 / 216
页数:8
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