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针对 mTOR 进行癌症治疗。

Targeting mTOR for cancer therapy.

机构信息

State Key Laboratory of Biotherapy, Laboratory of Stem Cell Biology, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, 610041, China.

Laboratory of Oncogene, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

出版信息

J Hematol Oncol. 2019 Jul 5;12(1):71. doi: 10.1186/s13045-019-0754-1.

Abstract

Mechanistic target of rapamycin (mTOR) is a protein kinase regulating cell growth, survival, metabolism, and immunity. mTOR is usually assembled into several complexes such as mTOR complex 1/2 (mTORC1/2). In cooperation with raptor, rictor, LST8, and mSin1, key components in mTORC1 or mTORC2, mTOR catalyzes the phosphorylation of multiple targets such as ribosomal protein S6 kinase β-1 (S6K1), eukaryotic translation initiation factor 4E binding protein 1 (4E-BP1), Akt, protein kinase C (PKC), and type-I insulin-like growth factor receptor (IGF-IR), thereby regulating protein synthesis, nutrients metabolism, growth factor signaling, cell growth, and migration. Activation of mTOR promotes tumor growth and metastasis. Many mTOR inhibitors have been developed to treat cancer. While some of the mTOR inhibitors have been approved to treat human cancer, more mTOR inhibitors are being evaluated in clinical trials. Here, we update recent advances in exploring mTOR signaling and the development of mTOR inhibitors for cancer therapy. In addition, we discuss the mechanisms underlying the resistance to mTOR inhibitors in cancer cells.

摘要

雷帕霉素靶蛋白(mTOR)是一种调节细胞生长、存活、代谢和免疫的蛋白激酶。mTOR 通常组装成几个复合物,如 mTOR 复合物 1/2(mTORC1/2)。在与 Raptor、rictor、LST8 和 mSin1 等 mTORC1 或 mTORC2 的关键成分合作下,mTOR 催化多个靶标的磷酸化,如核糖体蛋白 S6 激酶β-1(S6K1)、真核翻译起始因子 4E 结合蛋白 1(4E-BP1)、Akt、蛋白激酶 C(PKC)和 I 型胰岛素样生长因子受体(IGF-IR),从而调节蛋白质合成、营养物质代谢、生长因子信号、细胞生长和迁移。mTOR 的激活促进肿瘤生长和转移。已经开发出许多 mTOR 抑制剂来治疗癌症。虽然一些 mTOR 抑制剂已被批准用于治疗人类癌症,但更多的 mTOR 抑制剂正在临床试验中进行评估。在这里,我们更新了探索 mTOR 信号和开发 mTOR 抑制剂用于癌症治疗的最新进展。此外,我们还讨论了癌细胞对 mTOR 抑制剂产生耐药性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e03f/6612215/8cc7f209580a/13045_2019_754_Fig1_HTML.jpg

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