SMAC模拟物在癌症中的进展和前景综述:它是灵丹妙药吗?

Q4 Pharmacology, Toxicology and Pharmaceutics
E. Almuradova, Durr-e-shahwar Malik, Sara Yousaf, A. Farooqi
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引用次数: 0

摘要

细胞凋亡的缺失导致癌细胞的存活和不受控制的增殖。基础和临床研究人员已经解剖了无数细胞凋亡的中枢调节因子。第二线粒体源性半胱天蛋白酶激活剂(SMAC)/低pI直接抑制凋亡蛋白(IAP)结合蛋白(DIABLO)因其引发凋亡死亡的惊人能力而引起了人们的极大关注。因此,不同的跨学科研究团队正在设计和开发能够显著抑制原发性和继发性肿瘤生长的SMAC模拟物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overview of the progress and prospects of SMAC mimetics in cancers: Is it a silver bullet?
Loss of apoptosis results in the survival and uncontrolled proliferation of cancer cells. Basic and clinical researchers have dissected myriads of central regulators of apoptosis. Second mitochondria-derived activator of caspases (SMAC)/ direct inhibitor of apoptosis protein (IAP)-binding protein with low pI (DIABLO) has attracted phenomenal attention because of its amazing ability to trigger apoptotic death. Accordingly, different teams of interdisciplinary researchers are working on the design and development of SMAC mimetics which can significantly inhibit primary and secondary tumor growth.
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
自引率
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发文量
19
审稿时长
12 weeks
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