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Nrf2/Keap1信号通路在癌症预防/促进及化疗耐药中的矛盾作用

Contradictory roles of Nrf2/Keap1 signaling pathway in cancer prevention/promotion and chemoresistance.

作者信息

Jeddi Farhad, Soozangar Narges, Sadeghi Mohammad Reza, Somi Mohammad Hossein, Samadi Nasser

机构信息

Liver and Gastrointestinal Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Molecular Medicine, School of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

DNA Repair (Amst). 2017 Jun;54:13-21. doi: 10.1016/j.dnarep.2017.03.008. Epub 2017 Apr 3.

Abstract

NF-E2-related factor 2 (Nrf2) protein is a cytosolic transcription factor that regulates antioxidant and stress-related enzymes. Kelch-like ECH-associated protein 1 (Keap1) binds Nrf2 and accelerates ubiquitination and proteasome-dependent degradation of Nrf2. Nrf2 modifies the sensitivity of the cell environment to electrophiles and oxidants by inducing the transcriptional activation of more than 100 detoxification and cytoprotective genes. Prior investigations have found documentary evidence indicating that temporary activation of Nrf2 by pharmaceutical inducers plays a protective role against cancer initiation in normal cells. The impact of Nrf2/Keap1 pathway in development of tumorigenesis and drug resistance has also been well documented. Inhibition of the permanent Nrf2 activation, especially in combination with chemotherapeutics against cancer, may be considered as an important strategy to inhibit tumor growth and overcome chemoresistance. Here, we review the importance of Nrf2-keap1 pathway in the prevention or promotion of cancer, and resistance mechanisms to chemotherapeutic agents.

摘要

核因子E2相关因子2(Nrf2)蛋白是一种胞质转录因子,可调节抗氧化和应激相关酶。 Kelch样ECH相关蛋白1(Keap1)结合Nrf2并加速Nrf2的泛素化和蛋白酶体依赖性降解。 Nrf2通过诱导100多个解毒和细胞保护基因的转录激活来改变细胞环境对亲电试剂和氧化剂的敏感性。先前的研究已发现文献证据表明,药物诱导剂对Nrf2的临时激活在正常细胞中对癌症起始具有保护作用。 Nrf2 / Keap1途径在肿瘤发生和耐药性发展中的影响也有充分记录。抑制Nrf2的永久激活,特别是与抗癌化疗药物联合使用时,可能被视为抑制肿瘤生长和克服化疗耐药性的重要策略。在此,我们综述了Nrf2-keap1途径在预防或促进癌症以及对化疗药物的耐药机制中的重要性。

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