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靶向 mTOR 激酶结构域:第二代 mTOR 抑制剂。

Targeting the mTOR kinase domain: the second generation of mTOR inhibitors.

机构信息

Cancer Institute of New Jersey, Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

出版信息

Drug Discov Today. 2011 Apr;16(7-8):325-31. doi: 10.1016/j.drudis.2011.02.008. Epub 2011 Feb 17.

Abstract

The mTOR signaling pathway is dysregulated in ∼50% of all human malignancies and is a major cancer drug target. Although rapamycin analogs (rapalogs) have shown clinical efficacy in a subset of cancers, they do not fully exploit the antitumor potential of mTOR targeting. Because the mTOR kinase domain is important for rapamycin-sensitive and -insensitive functions, mTOR catalytic inhibitors have been developed recently as the second generation of anti-mTOR agents. Importantly, they have shown marked improvement of antitumor activity in vivo and in vitro. This review will detail the potential therapeutic value and issues of these novel antineoplastic agents, with emphasis placed on those that have already entered clinical trials.

摘要

mTOR 信号通路在所有人类恶性肿瘤中约有 50%失调,是癌症药物的主要靶点。虽然雷帕霉素类似物(rapalog)在一部分癌症中显示出临床疗效,但它们并没有充分发挥 mTOR 靶向的抗肿瘤潜力。由于 mTOR 激酶结构域对于雷帕霉素敏感和不敏感的功能都很重要,因此最近已经开发出 mTOR 催化抑制剂作为第二代抗 mTOR 药物。重要的是,它们在体内和体外都显示出明显改善的抗肿瘤活性。这篇综述将详细介绍这些新型抗肿瘤药物的潜在治疗价值和问题,重点介绍那些已经进入临床试验的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be1d/3073023/fdb80a9aadda/nihms277443f1.jpg

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