摘要
髓系细胞白血病1(Mcl-1)是具有抗凋亡活性的Bcl-2蛋白家族中的一个成员。它在调节细胞凋亡的内在途径中起着关键作用。此外,Mcl-1与各种癌症的进展和耐药性相关。Mcl-1抑制剂的开发可能提供有效的癌症治疗方法。虽然其他Bcl-2抗凋亡蛋白的抑制剂已经得到了很好的探索,但发现具有高选择性的Mcl-1抑制剂一直具有挑战性。本文综述了Mcl-1小分子和肽抑制剂的文献,分为肽抑制剂、棉酚衍生物、S1衍生物、醇衍生物、喹啉衍生物、S63845、AZD5991、AMG176等。并总结了它们的生物活性。Mcl-1是一种有效的药物靶点,用小分子抑制剂抑制Mcl-1是一种很有前途的癌症治疗策略。
关键词: 细胞凋亡、抗肿瘤药物、抗凋亡蛋白、Bcl-2家族蛋白、髓系细胞白血病1抑制剂。
Current Molecular Medicine
Title:Peptide and Small Molecule Inhibitors Targeting Myeloid Cell Leukemia 1 (Mcl-1) as Novel Antitumor Agents
Volume: 21 Issue: 5
关键词: 细胞凋亡、抗肿瘤药物、抗凋亡蛋白、Bcl-2家族蛋白、髓系细胞白血病1抑制剂。
摘要: Myeloid cell leukemia 1 (Mcl-1) is a member of the Bcl-2 family of proteins with anti-apoptotic activity. It plays a key role in the regulation of the intrinsic pathway of apoptosis. Moreover, Mcl-1 is correlated with the progression and drug-resistance of various cancers. The development of inhibitors of Mcl-1 may provide effective cancer therapies. While the inhibitors of other Bcl-2 anti-apoptotic proteins have been well explored, the discovery of Mcl-1inhibitors with high selectivity has been challenging. In this review, we summarize the recent literature on small molecule and peptide inhibitors of Mcl-1, which are divided into different types including peptide inhibitors, gossypol derivatives, marinopyrrole derivatives, S1 derivatives, indole derivatives, quinoline derivatives, S63845, AZD5991, AMG176, etc. Their biological activities are also summarized. Mcl-1 is a valid drug target and inhibition of Mcl-1 with a small molecule inhibitor is a promising strategy for cancer therapy.
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Cite this article as:
Peptide and Small Molecule Inhibitors Targeting Myeloid Cell Leukemia 1 (Mcl-1) as Novel Antitumor Agents, Current Molecular Medicine 2021; 21 (5) . https://dx.doi.org/10.2174/1566524020666200929121016
DOI https://dx.doi.org/10.2174/1566524020666200929121016 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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