Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy.
Department of Biomedical Sciences and Public Health, Section of Pathological Anatomy, Università Politecnica delle Marche, 60126 Ancona, Italy.
Front Biosci (Landmark Ed). 2023 Jul 21;28(7):143. doi: 10.31083/j.fbl2807143.
Prostate cancer is the second most common malignancy in men worldwide. Prostate cancer can be treated by surgery, radiotherapy and hormone therapy. The latter, in the form of androgen-deprivation therapy is needed to reduce prostate cancer progression at an advanced stage. Several studies demonstrated that oxidative stress is involved in cancer occurrence, development and progression and the Nuclear factor erythroid 2-related factor 2 (NRF2)/Kelch Like ECH Associated Protein 1 (KEAP1) pathway is affected by reactive oxygen species (ROS). Furthermore, the NRF2/KEAP1 signaling pathway has been investigated by several studies related to anti-androgen therapy, biochemical recurrence and radiotherapy. In this review we analysed the current literature regarding the indirect modulators involved in NRF2/KEAP1 pathway regulation and their role as possible therapeutic targets in prostate cancer cells.
前列腺癌是全球男性第二大常见恶性肿瘤。前列腺癌可以通过手术、放疗和激素治疗进行治疗。后者以去势治疗的形式用于减少晚期前列腺癌的进展。多项研究表明,氧化应激参与癌症的发生、发展和进展,核因子红细胞 2 相关因子 2(NRF2)/Kelch 样 ECH 相关蛋白 1(KEAP1)途径受活性氧(ROS)的影响。此外,已有多项研究探讨了 NRF2/KEAP1 信号通路与抗雄激素治疗、生化复发和放疗的关系。在这篇综述中,我们分析了目前关于 NRF2/KEAP1 通路调节中涉及的间接调节剂及其作为前列腺癌细胞潜在治疗靶点的作用的文献。