mTOR Signalling in Health and Disease

被引:50
作者
Proud, Christopher G. [1 ]
机构
[1] Univ Southampton, Sch Biol Sci, Southampton SO17 1BJ, Hants, England
关键词
mammalian target of rapamycin (mTOR); protein kinase; rapamycin; signalling; target of rapamycin (TOR); target of rapamycin complex (TORC); CELL-GROWTH; RAG GTPASES; KINASE; TOR; PHOSPHORYLATION; TRANSCRIPTION; INHIBITORS; RAPAMYCIN; PATHWAY;
D O I
10.1042/BST0390431
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The TOR (target of rapamycin) proteins are found in all eukaryotes. TOR has a protein kinase domain, as well as other domains through which it interacts with partner proteins to form at least two types of multiprotein complex, TORC1 and TORC2 (TOR complexes 1 and 2). Rapamycin, an antibiotic and immunosuppressant, inhibits functions of TORC1. Use of this drug has revealed roles for TORC1 and its mammalian counterpart, mTORC1, in promoting many anabolic processes. mTORC1 signalling is activated by growth factors and nutrients. It is highly active in many cancers and plays a role in tumorigenesis and in other diseases. Much less is known so far about the functions and regulation of (m)TORC2. The goal of this meeting was to bring together researchers studying the roles of mTORC1/2 in normal cell and animal physiology in diverse systems, as well as scientists exploring the therapeutic value of inhibiting mTOR (mammalian TOR) signalling.
引用
收藏
页码:431 / 436
页数:6
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