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Apo2L/TRAIL 诱导细胞凋亡信号的新见解。

New insights into apoptosis signaling by Apo2L/TRAIL.

机构信息

Department of Molecular Oncology, Genentech Inc., South San Francisco, CA, USA.

出版信息

Oncogene. 2010 Aug 26;29(34):4752-65. doi: 10.1038/onc.2010.221. Epub 2010 Jun 7.

Abstract

Apoptosis ligand 2 tumor necrosis factor (TNF)-related apoptosis-inducing ligand (Apo2L/TRAIL) belongs to a small subset of proapoptotic protein ligands in the TNF superfamily. This subset, which also includes Fas ligand and TNF-alpha, can activate the extrinsic apoptotic cell death pathway on binding to cognate death receptors at the cell surface. Over the past 10 years, Apo2L/TRAIL has emerged as a promising candidate for cancer therapy, on the basis of its unique ability to trigger apoptosis in various types of cancer cells without significant toxicity toward normal cells. Herein, we review key advances in understanding the molecular events that control apoptosis signaling by Apo2L/TRAIL, which may aid in the development of cancer therapies based on the extrinsic apoptotic pathway.

摘要

凋亡配体 2 肿瘤坏死因子(TNF)相关凋亡诱导配体(Apo2L/TRAIL)属于 TNF 超家族中促凋亡蛋白配体的一个小亚群。该亚群还包括 Fas 配体和 TNF-α,可在与细胞表面的同源死亡受体结合后激活细胞外凋亡细胞死亡途径。在过去的 10 年中,Apo2L/TRAIL 作为癌症治疗的有前途的候选药物出现,这是基于其在不引起正常细胞显著毒性的情况下触发各种类型癌细胞凋亡的独特能力。本文综述了理解 Apo2L/TRAIL 控制凋亡信号的分子事件的主要进展,这可能有助于基于细胞外凋亡途径的癌症治疗的发展。

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