mTOR pathway in colorectal cancer: an update

被引:155
作者
Francipane, Maria Giovanna [1 ,2 ]
Lagasse, Eric [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Pathol, McGowan Inst Regenerat Med, Pittsburgh, PA 15260 USA
[2] Ri MED Fdn, Palermo, Italy
关键词
mTOR; colorectal cancer; cancer stem-like cells; personalized medicine; DUAL PI3K/MTOR INHIBITOR; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; CELL-CYCLE ARREST; EXTENDS LIFE-SPAN; HISTONE DEACETYLASE INHIBITOR; REDUCES TUMOR-GROWTH; MAMMALIAN TARGET; IN-VITRO; RAPAMYCIN INHIBITOR; ANTITUMOR-ACTIVITY;
D O I
10.18632/oncotarget.1548
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mammalian target of rapamycin (mTOR) has emerged as a potential target for drug development, particularly due to the fact that it plays such a crucial role in cancer biology. In addition, next-generation mTOR inhibitors have become available, marking an exciting new phase in mTOR-based therapy. However, the verdict on their therapeutic effectiveness remains unclear. Here we review phosphatidylinositol-3-kinase (PI3K)/Akt/mTOR signaling as one of the primary mechanisms for sustaining tumor outgrowth and metastasis, recent advances in the development of mTOR inhibitors, and current studies addressing mTOR activation/inhibition in colorectal cancer (CRC). We will also discuss our recent comparative study of different mTOR inhibitors in a population of colon cancer stem cells (CSCs), and current major challenges for achieving individualized drug therapy using kinase inhibitors.
引用
收藏
页码:49 / 66
页数:18
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