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IAP蛋白家族、SMAC模拟物与癌症治疗

The IAP Protein Family, SMAC Mimetics and Cancer Treatment.

作者信息

Philchenkov Alex, Miura Koh

机构信息

R. E. Kavetsky Institute of Experimental Pathology, Oncology & Radiobiology Kyiv, Ukraine.

Department of Surgery, Miyagi Cancer Center, Natori, Miyagi, Japan.

出版信息

Crit Rev Oncog. 2016;21(3-4):185-202. doi: 10.1615/CritRevOncog.2016017032.

Abstract

Since the acquired resistance of cells to apoptosis is one of the major hallmarks of cancer, the endogenous inhibitors of apoptosis can be regarded as promising targets in the design of anticancer therapeutics. In addition to their antiapoptotic activity, inhibitor of apoptosis proteins (IAPs) are able to regulate numerous other cell functions, including proliferation, differentiation, and migration, as well as proinflammatory and immune responses. Study of the IAP family as target molecules in targeted therapies has recently focused on SMAC mimetics as synthetic IAP antagonists that have been under development as promising therapeutics. To overview the background of IAP proteins and to focus on the development of SMAC mimetics, the present review first looks at the mechanisms of IAP proteins' antiapoptotic activities and those for controlling those activities; then the SMAC mimetics, including birinapant, LCL161, and DEBIO1143/AT-406, and their clinical trials are introduced. To further clarify the processes to exert the efficacies of SMAC mimetics, it is necessary to determine therapeutic biomarkers that predict and assess them, which may include caspases and factors in the TNFα pathway.

摘要

由于细胞对凋亡的获得性抗性是癌症的主要标志之一,凋亡的内源性抑制剂可被视为抗癌治疗设计中很有前景的靶点。除了具有抗凋亡活性外,凋亡抑制蛋白(IAPs)还能够调节许多其他细胞功能,包括增殖、分化和迁移,以及促炎和免疫反应。最近,作为靶向治疗中的靶分子,对IAP家族的研究集中在SMAC模拟物上,它们是作为有前景的治疗药物正在开发的合成IAP拮抗剂。为了概述IAP蛋白的背景并聚焦于SMAC模拟物的开发,本综述首先探讨IAP蛋白抗凋亡活性的机制以及控制这些活性的机制;然后介绍包括比瑞那潘、LCL161和DEBIO1143/AT-406在内的SMAC模拟物及其临床试验。为了进一步阐明发挥SMAC模拟物疗效的过程,有必要确定预测和评估它们的治疗生物标志物,这可能包括半胱天冬酶和TNFα途径中的因子。

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