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凋亡抑制蛋白(IAP)是信号通路的关键调节因子,也是抗癌治疗的靶点。

The inhibitor of apoptosis (IAP) proteins are critical regulators of signaling pathways and targets for anti-cancer therapy.

作者信息

de Almagro M C, Vucic D

机构信息

Department of Early Discovery Biochemistry, Genentech, Inc., South San Francisco, CA 94080, USA.

出版信息

Exp Oncol. 2012 Oct;34(3):200-11.

Abstract

Cell death regulation is vital for maintenance of homeostasis and proper development of multicellular organisms. Inhibitor of apoptosis (IAP) proteins are implicated in multiple ways in cell death regulation, ranging from inhibition of apoptosis and necrosis to the regulation of cell cycle and inflammation. Due to their prominent ability to control cell death and elevated expression in a variety of cancer cell types, IAP proteins are attractive targets for the development of novel anti-cancer treatments. The most widely used strategy for targeting IAP proteins is based on mimicking the natural IAP antagonist, SMAC/DIABLO. IAP antagonists are currently being tested in humans and they were designed for anti-cancer therapy but they could potentially also be considered for treatments of the immune system disorders. In this manuscript we will review the functional roles of IAP proteins, specifically of c-IAP1, c-IAP2, ML-IAP and XIAP, and evaluate IAP targeting strategies for disease treatments. This article is part of a Special Issue entitled "Apoptosis: Four Decades Later".

摘要

细胞死亡调控对于维持多细胞生物体的内环境稳态和正常发育至关重要。凋亡抑制蛋白(IAP)以多种方式参与细胞死亡调控,范围从抑制凋亡和坏死到调节细胞周期和炎症。由于其控制细胞死亡的显著能力以及在多种癌细胞类型中的高表达,IAP蛋白是开发新型抗癌治疗的有吸引力的靶点。靶向IAP蛋白最广泛使用的策略是基于模拟天然IAP拮抗剂SMAC/DIABLO。IAP拮抗剂目前正在人体中进行测试,它们被设计用于抗癌治疗,但也有可能被考虑用于治疗免疫系统疾病。在本手稿中,我们将综述IAP蛋白的功能作用,特别是c-IAP1、c-IAP2、ML-IAP和XIAP的功能作用,并评估用于疾病治疗的IAP靶向策略。本文是名为“凋亡:四十年后”的特刊的一部分。

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