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1
Characterization of Rictor phosphorylation sites reveals direct regulation of mTOR complex 2 by S6K1.Rictor磷酸化位点的表征揭示了S6K1对mTOR复合物2的直接调控。
Mol Cell Biol. 2009 Nov;29(21):5657-70. doi: 10.1128/MCB.00735-09. Epub 2009 Aug 31.
2
Biochemical, cellular, and in vivo activity of novel ATP-competitive and selective inhibitors of the mammalian target of rapamycin.新型雷帕霉素哺乳动物靶点ATP竞争性选择性抑制剂的生化、细胞及体内活性
Cancer Res. 2009 Aug 1;69(15):6232-40. doi: 10.1158/0008-5472.CAN-09-0299. Epub 2009 Jul 7.
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AKT-independent signaling downstream of oncogenic PIK3CA mutations in human cancer.人类癌症中致癌性PIK3CA突变下游的非AKT依赖性信号传导。
Cancer Cell. 2009 Jul 7;16(1):21-32. doi: 10.1016/j.ccr.2009.04.012.
4
DEPTOR is an mTOR inhibitor frequently overexpressed in multiple myeloma cells and required for their survival.DEPTOR是一种mTOR抑制剂,在多发性骨髓瘤细胞中经常过度表达,是其生存所必需的。
Cell. 2009 May 29;137(5):873-86. doi: 10.1016/j.cell.2009.03.046. Epub 2009 May 14.
5
Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR).库-0063794是雷帕霉素哺乳动物靶点(mTOR)的特异性抑制剂。
Biochem J. 2009 Jun 12;421(1):29-42. doi: 10.1042/BJ20090489.
6
The pharmacology of mTOR inhibition.mTOR抑制的药理学
Sci Signal. 2009 Apr 21;2(67):pe24. doi: 10.1126/scisignal.267pe24.
7
Molecular mechanisms of mTOR-mediated translational control.mTOR介导的翻译控制的分子机制。
Nat Rev Mol Cell Biol. 2009 May;10(5):307-18. doi: 10.1038/nrm2672. Epub 2009 Apr 2.
8
Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2.mTOR的活性位点抑制剂靶向mTORC1和mTORC2的雷帕霉素抗性输出。
PLoS Biol. 2009 Feb 10;7(2):e38. doi: 10.1371/journal.pbio.1000038.
9
PI3K and mTOR inhibitors: a new generation of targeted anticancer agents.PI3K和mTOR抑制剂:新一代靶向抗癌药物。
Curr Opin Cell Biol. 2009 Apr;21(2):194-8. doi: 10.1016/j.ceb.2008.12.011. Epub 2009 Feb 7.
10
mTOR complex 2 is required for the development of prostate cancer induced by Pten loss in mice.mTOR复合物2是小鼠中由Pten缺失诱导的前列腺癌发生所必需的。
Cancer Cell. 2009 Feb 3;15(2):148-59. doi: 10.1016/j.ccr.2008.12.017.

mTOR 与癌症:一条通路上的多个环。

mTOR and cancer: many loops in one pathway.

机构信息

Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, United States.

出版信息

Curr Opin Cell Biol. 2010 Apr;22(2):169-76. doi: 10.1016/j.ceb.2009.10.007. Epub 2009 Nov 27.

DOI:10.1016/j.ceb.2009.10.007
PMID:19945836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2854285/
Abstract

The mammalian target of rapamycin (mTOR) is a master regulator of cell growth and division that responds to a variety of stimuli, including nutrient, energy, and growth factors. In the last years, a significant number of pieces have been added to the puzzle of how mTOR coordinates and executes its functions. Extensive research on mTOR has also uncovered a complex network of regulatory loops that impact the therapeutic approaches aimed at targeting mTOR.

摘要

哺乳动物雷帕霉素靶蛋白(mTOR)是细胞生长和分裂的主要调节因子,对各种刺激(包括营养、能量和生长因子)作出反应。在过去几年中,人们对 mTOR 如何协调和执行其功能有了更多的了解。对 mTOR 的广泛研究还揭示了一个复杂的调节环网络,这些调节环网络影响着靶向 mTOR 的治疗方法。