The mTOR pathway in hepatic malignancies

被引:108
作者
Bhat, Mamatha [1 ,2 ,3 ]
Sonenberg, Nahum [2 ]
Gores, Gregory J. [3 ]
机构
[1] McGill Univ, Div Gastroenterol, Ctr Hlth, Montreal, PQ, Canada
[2] McGill Univ, Dept Biochem, Goodman Canc Res Ctr, Montreal, PQ, Canada
[3] Mayo Clin, Div Gastroenterol & Hepatol, Coll Med, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
HEPATOCELLULAR-CARCINOMA; MAMMALIAN TARGET; INHIBITS GROWTH; IN-VITRO; LIVER-TRANSPLANTATION; PHOSPHO-MTOR; RAPAMYCIN; SIROLIMUS; METFORMIN; PTEN;
D O I
10.1002/hep.26323
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The mechanistic/mammalian target of rapamycin (mTOR) pathway plays a critical role in cellular metabolism, growth, and proliferation and has been evaluated as a target for therapy in various malignancies. The mTOR pathway is a major tumor-initiating pathway in hepatocellular carcinoma, with up-regulation seen in up to 50% of tumors. Metformin, which represses mTOR signaling by activating adenosine monophosphate-activated protein kinase, has been shown to decrease liver carcinogenesis in population studies. mTOR inhibitors such as everolimus have been evaluated as adjunctive chemotherapy with some success, although efficacy has been limited by the lack of complete mTOR pathway inhibition. The active site mTOR inhibitors hold greater promise, given that they offer complete mTOR suppression. There is also evidence of mTOR pathway activation in cholangiocarcinoma, although its biological significance in initiating and promoting tumor progression remains ambiguous. This review provides an overview of the complex biochemistry behind the mTOR pathway and its role in carcinogenesis, especially as it pertains to hepatic malignancies. (HEPATOLOGY 2013;58:810-818)
引用
收藏
页码:810 / 818
页数:9
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