Twenty-five years of mTOR: Uncovering the link from nutrients to growth

被引:393
作者
Sabatini, David M. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02142 USA
[4] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
[5] Broad Inst Harvard & Massachusetts Inst Technol, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
mTOR; rapamycin; nutrients; Rag GTPase; growth; P70; S6; KINASE; TUBEROUS SCLEROSIS COMPLEX; TUMOR-SUPPRESSOR COMPLEX; AMINO-ACID SUFFICIENCY; CELL-GROWTH; RAG GTPASES; RAPAMYCIN AY-22,989; MAMMALIAN PROTEIN; MACROLIDES FK-506; BINDING PARTNER;
D O I
10.1073/pnas.1716173114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In my PNAS Inaugural Article, I describe the development of the mTOR field, starting with efforts to understand the mechanism of action of the drug rapamycin, which similar to 25 y ago led to the discovery of the mTOR protein kinase. I focus on insights that we have contributed and on work that has been particularly influential to me, as well as provide some personal reflections and stories. We now appreciate that, as part of two distinct complexes, mTORC1 and mTORC2, mTOR is the major regulator of growth (mass accumulation) in animals and is the key link between the availability of nutrients in the environment and the control of most anabolic and catabolic processes. Nutrients signal to mTORC1 through the lysosome-associated Rag GTPases and their many regulators and associated cytosolic and lysosomal nutrient sensors. mTOR signaling is deregulated in common diseases, like cancer and epilepsy, and mTORC1 is a well-validated modulator of aging in multiple model organisms. There is significant excitement around using mTORC1 inhibitors to treat cancer and neurological disease and, potentially, to improve healthspan and lifespan.
引用
收藏
页码:11818 / 11825
页数:8
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