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雷帕霉素哺乳动物靶点在肉瘤中的抑制机制:现状与未来

Mechanisms of mammalian target of rapamycin inhibition in sarcoma: present and future.

作者信息

MacKenzie Amy R, von Mehren Margaret

机构信息

Temple University Hospital, Internal Medicine, 3401 N. Broad St. 8PP, Philadelphia, PA 19140, USA.

出版信息

Expert Rev Anticancer Ther. 2007 Aug;7(8):1145-54. doi: 10.1586/14737140.7.8.1145.

Abstract

The mammalian target of rapamycin (mTOR) is a protein kinase that plays a pivotal role in the control of cell growth and development. A part of the PI3K/Akt pathway, mTOR responds to growth factor stimuli as well as nutrient availability by variations in downstream phosphorylation. Increasing knowledge of the upstream regulators and downstream targets of mTOR has led to the development of anticancer drugs that suppress protein synthesis and metabolism. Rapamycin (sirolimus) and three rapamycin analogues are currently being evaluated in clinical trials: temsirolimus (CCI-779, Wyeth), everolimus (RAD001, Novartis Pharma AG), and AP23573 (Ariad Pharmaceuticals Inc.). This review will highlight the role of these inhibitors in the treatment of sarcoma.

摘要

雷帕霉素的哺乳动物靶点(mTOR)是一种蛋白激酶,在细胞生长和发育的调控中起关键作用。作为PI3K/Akt信号通路的一部分,mTOR通过下游磷酸化的变化对生长因子刺激以及营养物质的可利用性作出反应。对mTOR上游调节因子和下游靶点的了解不断增加,促使了抑制蛋白质合成和代谢的抗癌药物的研发。雷帕霉素(西罗莫司)和三种雷帕霉素类似物目前正在临床试验中进行评估:替西罗莫司(CCI-779,惠氏公司)、依维莫司(RAD001,诺华制药有限公司)和AP23573(阿里阿德制药公司)。本综述将重点介绍这些抑制剂在肉瘤治疗中的作用。

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