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一种对抗金属药物耐药性的新策略:通过自噬靶向线粒体以抑制癌细胞的代谢适应。

A New Strategy to Fight Metallodrug Resistance: Mitochondria-Relevant Treatment through Mitophagy to Inhibit Metabolic Adaptations of Cancer Cells.

机构信息

Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.

Department of Rheumatology and Immunology, Jinling Hospital, Medical School of Nanjing University, Nanjing, 210002, China.

出版信息

Angew Chem Int Ed Engl. 2022 Jul 4;61(27):e202203843. doi: 10.1002/anie.202203843. Epub 2022 May 5.

Abstract

Metabolic adaptations can help cancer cells to escape from chemotherapeutics, mainly involving autophagy and ATP production. Herein, we report a new rhein-based cyclometalated Ir complex, Ir-Rhein, that can accurately target mitochondria and effectively inhibit metabolic adaptations. The complex Ir-Rhein induces severe mitochondrial damage and initiates mitophagy to reduce the number of mitochondria and subsequently inhibit both mitochondrial and glycolytic bioenergetics, which eventually leads to ATP starvation death. Moreover, Ir-Rhein can overcome cisplatin resistance. Co-incubation experiment, 3D tumor spheroids experiment and transcriptome analysis reveal that Ir-Rhein shows promising antiproliferation performance for cisplatin-resistant cancer cells with the regulation of platinum resistance-related transporters. To our knowledge, this is a new strategy to overcome metallodrug resistance with a mitochondria-relevant treatment.

摘要

代谢适应可以帮助癌细胞逃避化疗药物,主要涉及自噬和 ATP 产生。在此,我们报告了一种基于大黄酸的新型金属铱配合物 Ir-Rhein,它可以精确靶向线粒体并有效抑制代谢适应。该配合物 Ir-Rhein 诱导严重的线粒体损伤并启动自噬,以减少线粒体数量,进而抑制线粒体和糖酵解生物能量,最终导致 ATP 饥饿死亡。此外,Ir-Rhein 可以克服顺铂耐药性。共孵育实验、3D 肿瘤球实验和转录组分析表明,Ir-Rhein 通过调节铂耐药相关转运体,对顺铂耐药癌细胞表现出有前途的抗增殖作用。据我们所知,这是一种用与线粒体相关的治疗方法来克服金属药物耐药性的新策略。

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