School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, 2052, Australia.
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, 2052, Australia.
Mol Metab. 2021 Sep;51:101222. doi: 10.1016/j.molmet.2021.101222. Epub 2021 Mar 26.
Mitochondrial uncouplers are well-known for their ability to treat a myriad of metabolic diseases, including obesity and fatty liver diseases. However, for many years now, mitochondrial uncouplers have also been evaluated in diverse models of cancer in vitro and in vivo. Furthermore, some mitochondrial uncouplers are now in clinical trials for cancer, although none have yet been approved for the treatment of cancer.
In this review we summarise published studies in which mitochondrial uncouplers have been investigated as an anti-cancer therapy in preclinical models. In many cases, mitochondrial uncouplers show strong anti-cancer effects both as single agents, and in combination therapies, and some are more toxic to cancer cells than normal cells. Furthermore, the mitochondrial uncoupling mechanism of action in cancer cells has been described in detail, with consistencies and inconsistencies between different structural classes of uncouplers. For example, many mitochondrial uncouplers decrease ATP levels and disrupt key metabolic signalling pathways such as AMPK/mTOR but have different effects on reactive oxygen species (ROS) production. Many of these effects oppose aberrant phenotypes common in cancer cells that ultimately result in cell death. We also highlight several gaps in knowledge that need to be addressed before we have a clear direction and strategy for applying mitochondrial uncouplers as anti-cancer agents.
There is a large body of evidence supporting the therapeutic use of mitochondrial uncouplers to treat cancer. However, the long-term safety of some uncouplers remains in question and it will be critical to identify which patients and cancer types would benefit most from these agents.
线粒体解偶联剂以其治疗多种代谢疾病的能力而闻名,包括肥胖症和脂肪肝疾病。然而,多年来,线粒体解偶联剂也在各种体外和体内癌症模型中进行了评估。此外,一些线粒体解偶联剂目前正在进行癌症的临床试验,尽管尚无一种药物被批准用于癌症治疗。
在这篇综述中,我们总结了已发表的研究,这些研究将线粒体解偶联剂作为一种癌症治疗方法在临床前模型中进行了研究。在许多情况下,线粒体解偶联剂作为单一药物以及联合治疗方法均显示出强大的抗癌作用,并且一些药物对癌细胞的毒性比对正常细胞的毒性更大。此外,还详细描述了癌细胞中线粒体解偶联作用的机制,不同结构类型的解偶联剂之间存在一致性和不一致性。例如,许多线粒体解偶联剂会降低 ATP 水平并破坏关键的代谢信号通路,如 AMPK/mTOR,但对活性氧(ROS)的产生有不同的影响。这些作用中的许多作用与癌细胞中常见的异常表型相抗衡,最终导致细胞死亡。我们还强调了一些需要解决的知识空白,以便我们能够清楚地确定将线粒体解偶联剂作为抗癌药物的应用方向和策略。
有大量证据支持使用线粒体解偶联剂治疗癌症的治疗用途。但是,一些解偶联剂的长期安全性仍存在疑问,确定哪些患者和癌症类型最能从这些药物中受益将是至关重要的。