NRF2 activation in cancer and overview of NRF2 small molecule inhibitors

IF 7.5 3区 医学 Q1 CHEMISTRY, MEDICINAL
Hoang Hai Ngo, Bo-Yeong Yu, Jeong-Eun Lee, Hyunwoo Kim, Young-Sam Keum
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引用次数: 0

Abstract

NRF2 is a redox-sensitive transcription factor that activates the expression of phase II detoxifying and antioxidant enzymes. In addition to maintaining redox homeostasis, NRF2 regulates various other processes, including metabolism, stem cell renewal, mitochondrial function, and proteostasis. NRF2 is considered a tumor suppressor because its activation by chemopreventive phytochemicals contributes to the detoxification of oxidants and electrophiles in normal cells. However, aberrant NRF2 activation occurs in cancer due to mutations in the KEAP1/NRF2 pathway, and it contributes to the generation of a tumor microenvironment that favors the proliferation, survival, and chemoresistance of cancer cells. In this review, we present the regulatory mechanisms of NRF2 and discuss how NRF2 activation contributes to chemoresistance. We also explain therapeutic strategies that exploit the vulnerabilities of NRF2-addicted cancer cells, providing NRF2 small-molecule inhibitors along with their mechanisms of action.

NRF2在癌症中的激活及NRF2小分子抑制剂综述。
NRF2是一种氧化还原敏感转录因子,可激活II期解毒和抗氧化酶的表达。除了维持氧化还原稳态外,NRF2还调节各种其他过程,包括代谢、干细胞更新、线粒体功能和蛋白质稳态。NRF2被认为是一种肿瘤抑制因子,因为它被化学预防植物化学物质激活,有助于正常细胞中氧化剂和亲电试剂的解毒。然而,由于KEAP1/NRF2通路的突变,NRF2异常激活在癌症中发生,它有助于肿瘤微环境的产生,有利于癌细胞的增殖、存活和化疗耐药。在这篇综述中,我们介绍了NRF2的调控机制,并讨论了NRF2的激活如何促进化学耐药。我们还解释了利用NRF2成瘾癌细胞的脆弱性的治疗策略,提供了NRF2小分子抑制剂及其作用机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
13.40
自引率
9.00%
发文量
48
审稿时长
3.3 months
期刊介绍: Archives of Pharmacal Research is the official journal of the Pharmaceutical Society of Korea and has been published since 1976. Archives of Pharmacal Research is an interdisciplinary journal devoted to the publication of original scientific research papers and reviews in the fields of drug discovery, drug development, and drug actions with a view to providing fundamental and novel information on drugs and drug candidates.
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