Inhibitors of Apoptosis Proteins (IAPs): Clinical Significance in Cancer Treatment Research

K. Tewari, S. Dhaneshwar
{"title":"Inhibitors of Apoptosis Proteins (IAPs): Clinical Significance in Cancer Treatment Research","authors":"K. Tewari, S. Dhaneshwar","doi":"10.6000/1929-2279.2012.01.02.7","DOIUrl":null,"url":null,"abstract":"Apoptosis is a process, which involves a sequence of cellular changes, which ultimately lead to cell death. This programmed cell death is a normal phenomenon required for growth of an organism. Inhibition of apoptosis can result in a number of cancers, inflammatory and autoimmune diseases and viral infections. Inhibitors of apoptosis proteins (IAPs) are a family of structurally and functionally related proteins, which play a crucial role in apoptosis (programmed cell death), proliferation and angiogenesis. Till date 8 IAPs have been identified (Survivin, XIAP, Livin, cellular IAP 1 and 2, ILP-2, NAIP and BRUCE/Apollon). The current review discusses individual protein in details with respect to its structural features, functions and clinical significance. These proteins; especially survivin, XIAP and Livin have been found to express in wide range of malignancies and hence taken as a target of interest by various research groups. The review also highlights the various Phase- 1 and 2 studies of new therapeutic agents that are being developed either as a monotherapy or in combination with existent drugs, which target these IAPs.","PeriodicalId":89799,"journal":{"name":"Journal of cancer research updates","volume":"1 1","pages":"212-220"},"PeriodicalIF":0.0000,"publicationDate":"2012-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cancer research updates","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6000/1929-2279.2012.01.02.7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Apoptosis is a process, which involves a sequence of cellular changes, which ultimately lead to cell death. This programmed cell death is a normal phenomenon required for growth of an organism. Inhibition of apoptosis can result in a number of cancers, inflammatory and autoimmune diseases and viral infections. Inhibitors of apoptosis proteins (IAPs) are a family of structurally and functionally related proteins, which play a crucial role in apoptosis (programmed cell death), proliferation and angiogenesis. Till date 8 IAPs have been identified (Survivin, XIAP, Livin, cellular IAP 1 and 2, ILP-2, NAIP and BRUCE/Apollon). The current review discusses individual protein in details with respect to its structural features, functions and clinical significance. These proteins; especially survivin, XIAP and Livin have been found to express in wide range of malignancies and hence taken as a target of interest by various research groups. The review also highlights the various Phase- 1 and 2 studies of new therapeutic agents that are being developed either as a monotherapy or in combination with existent drugs, which target these IAPs.
凋亡蛋白抑制剂在癌症治疗研究中的临床意义
细胞凋亡是一个过程,涉及一系列细胞变化,最终导致细胞死亡。这种程序性细胞死亡是生物体生长所必需的正常现象。抑制细胞凋亡可导致许多癌症、炎症和自身免疫性疾病以及病毒感染。凋亡蛋白抑制剂(IAPs)是一个结构和功能相关的蛋白家族,在细胞凋亡(程序性细胞死亡)、增殖和血管生成中起着至关重要的作用。到目前为止,已经确定了8个IAP (Survivin, XIAP, Livin, cellular IAP 1和2,ILP-2, NAIP和BRUCE/Apollon)。本文对单个蛋白的结构特征、功能和临床意义进行了详细的讨论。这些蛋白质;特别是survivin、XIAP和Livin已被发现在多种恶性肿瘤中表达,因此被各种研究小组视为感兴趣的靶标。该综述还重点介绍了针对这些iap的新治疗药物的各种1期和2期研究,这些新治疗药物正在作为单一疗法或与现有药物联合开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.20
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信