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靶向X连锁凋亡抑制蛋白用于恶性肿瘤治疗

Targeting XIAP for the treatment of malignancy.

作者信息

Schimmer A D, Dalili S, Batey R A, Riedl S J

机构信息

The Ontario Cancer Institute, Toronto, Ontario, Canada.

出版信息

Cell Death Differ. 2006 Feb;13(2):179-88. doi: 10.1038/sj.cdd.4401826.

Abstract

X-linked inhibitor of apoptosis protein (XIAP) is a member of the inhibitor of apoptosis proteins family of caspase inhibitors that selectively binds and inhibits caspases-3, -7 and -9, but not caspase-8. As such, XIAP blocks a substantial portion of the apoptosis pathway and is an attractive target for novel therapeutic agents for the treatment of malignancy. Antisense oligonucleotides directed against XIAP are effective in vitro and are currently being evaluated in clinical trials. Small molecule XIAP inhibitors that target the baculovirus IAP repeat (BIR) 2 or BIR 3 domain are in preclinical development and are advancing toward the clinic. This review will discuss the progress being made in developing antisense and small-molecule XIAP inhibitors.

摘要

X连锁凋亡抑制蛋白(XIAP)是凋亡抑制蛋白家族中半胱天冬酶抑制剂的一员,它能选择性地结合并抑制半胱天冬酶-3、-7和-9,但不抑制半胱天冬酶-8。因此,XIAP阻断了大部分凋亡途径,是治疗恶性肿瘤新型治疗药物的一个有吸引力的靶点。针对XIAP的反义寡核苷酸在体外有效,目前正在进行临床试验评估。靶向杆状病毒IAP重复序列(BIR)2或BIR 3结构域的小分子XIAP抑制剂正处于临床前开发阶段,并正在向临床推进。本综述将讨论在开发反义及小分子XIAP抑制剂方面取得的进展。

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