Abdalbari Farah H, Telleria Carlos M
Experimental Pathology Unit, Department of Pathology, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, Canada.
Cancer Research Program, Research Institute, McGill University Health Centre, Montreal, QC, Canada.
Discov Oncol. 2021 Oct 20;12(1):42. doi: 10.1007/s12672-021-00439-0.
Advanced stages of cancer are highly associated with short overall survival in patients due to the lack of long-term treatment options following the standard form of care. New options for cancer therapy are needed to improve the survival of cancer patients without disease recurrence. Auranofin is a clinically approved agent against rheumatoid arthritis that is currently enrolled in clinical trials for potential repurposing against cancer. Auranofin mainly targets the anti-oxidative system catalyzed by thioredoxin reductase (TrxR), which protects the cell from oxidative stress and death in the cytoplasm and the mitochondria. TrxR is over-expressed in many cancers as an adaptive mechanism for cancer cell proliferation, rendering it an attractive target for cancer therapy, and auranofin as a potential therapeutic agent for cancer. Inhibiting TrxR dysregulates the intracellular redox state causing increased intracellular reactive oxygen species levels, and stimulates cellular demise. An alternate mechanism of action of auranofin is to mimic proteasomal inhibition by blocking the ubiquitin-proteasome system (UPS), which is critically important in cancer cells to prevent cell death when compared to non-cancer cells, because of its role on cell cycle regulation, protein degradation, gene expression, and DNA repair. This article provides new perspectives on the potential mechanisms used by auranofin alone, in combination with diverse other compounds, or in combination with platinating agents and/or immune checkpoint inhibitors to combat cancer cells, while assessing the feasibility for its repurposing in the clinical setting.
由于在标准治疗模式后缺乏长期治疗选择,癌症晚期与患者的总体生存期短高度相关。需要新的癌症治疗选择来提高癌症患者的生存率且无疾病复发。金诺芬是一种临床上已获批用于治疗类风湿性关节炎的药物,目前正在进行临床试验,以探索其用于治疗癌症的潜在新用途。金诺芬主要靶向由硫氧还蛋白还原酶(TrxR)催化的抗氧化系统,该系统可保护细胞免受细胞质和线粒体中的氧化应激及死亡影响。TrxR在许多癌症中过度表达,作为癌细胞增殖的一种适应性机制,使其成为癌症治疗的一个有吸引力的靶点,而金诺芬则作为一种潜在的癌症治疗药物。抑制TrxR会使细胞内氧化还原状态失调,导致细胞内活性氧水平升高,并刺激细胞死亡。金诺芬的另一种作用机制是通过阻断泛素 - 蛋白酶体系统(UPS)来模拟蛋白酶体抑制作用,在癌细胞中,与非癌细胞相比,UPS在防止细胞死亡方面至关重要,因为它在细胞周期调控、蛋白质降解、基因表达和DNA修复中发挥作用。本文提供了关于金诺芬单独使用、与多种其他化合物联合使用,或与铂类药物和/或免疫检查点抑制剂联合使用以对抗癌细胞的潜在机制的新观点,同时评估了其在临床环境中重新应用的可行性。