前列腺癌中NRF2/KEAP1信号通路的细胞调节器
Giovanni Tossetta1, Sonia Fantone1, Daniela Marzioni1
1Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy.
Frontiers in bioscience (Landmark edition)
|August 1, 2023
概括
本综述探讨了前列腺癌中核因子红色素2相关因子2 (NRF2) /凯尔奇样ECH相关蛋白1 (KEAP1) 途径. 它确定了这种途径的间接调节器作为晚期疾病的潜在治疗点.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 前列腺癌是全球男性的主要恶性瘤.
- 雄激素缺失治疗对于晚期前列腺癌的治疗至关重要.
- 氧化应激和NRF2/KEAP1通路与癌症的发展和进展有关.
研究的目的:
- 对前列腺癌中NRF2/KEAP1通路的间接调节剂的当前文献进行审查.
- 探索这些调节器作为潜在的治疗点的作用.
主要方法:
- 对调查前列腺癌中NRF2/KEAP1通路的研究进行文献综述.
- 对影响NRF2/KEAP1信号的间接调节器的分析.
- 检查该途径与抗雄激素治疗,复发和放射治疗的相关性.
主要成果:
- NRF2/KEAP1通路受到活性氧物种 (ROS) 的影响.
- 这一途径与抗雄激素治疗,生化复发和前列腺癌放射治疗有关.
- 已经确定了NRF2/KEAP1通路的几个间接调节器.
结论:
- NRF2/KEAP1通路的间接调节器代表了前列腺癌的有希望的治疗点.
- 针对这些调节器可能为晚期前列腺癌提供新的治疗策略.
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