Mita Alain C, Mita Monica M, Nawrocki Steffan T, Giles Francis J
Institute for Drug Development, Cancer Therapy and Research Center at the University of Texas Health Science Center, 7979 Wurzbach Road, San Antonio, TX 78229, USA.
Clin Cancer Res. 2008 Aug 15;14(16):5000-5. doi: 10.1158/1078-0432.CCR-08-0746.
Survivin, a member of the family of inhibitor of apoptosis proteins, functions as a key regulator of mitosis and programmed cell death. Initially, survivin was described as an inhibitor of caspase-9. However, over the last years, research studies have shown that the role of survivin in cancer pathogenesis is not limited to apoptosis inhibition but also involves the regulation of the mitotic spindle checkpoint and the promotion of angiogenesis and chemoresistance. Survivin gene expression is transcriptionally repressed by wild-type p53 and can be deregulated in cancer by several mechanisms, including gene amplification, hypomethylation, increased promoter activity, and loss of p53 function. This article reviews the multiple functions of survivin in the regulation of apoptosis, the promotion of tumorigenesis, and the development of survivin inhibitors as a novel anticancer therapeutic strategy.
生存素是凋亡抑制蛋白家族的一员,作为有丝分裂和程序性细胞死亡的关键调节因子发挥作用。最初,生存素被描述为半胱天冬酶-9的抑制剂。然而,在过去几年中,研究表明生存素在癌症发病机制中的作用不仅限于抑制细胞凋亡,还涉及有丝分裂纺锤体检查点的调节以及血管生成和化疗耐药性的促进。生存素基因表达受到野生型p53的转录抑制,并且在癌症中可通过多种机制失调,包括基因扩增、低甲基化、启动子活性增加和p53功能丧失。本文综述了生存素在细胞凋亡调节、肿瘤发生促进以及作为新型抗癌治疗策略的生存素抑制剂开发中的多种功能。