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  2. Consolidating Organometallic Complex Ir-CA Empowers Mitochondria-Directed Chemotherapy against Resistant Cancer via Stemness and Metastasis Inhibition

Consolidating Organometallic Complex Ir-CA Empowers Mitochondria-Directed Chemotherapy against Resistant Cancer via Stemness and Metastasis Inhibition

  • Inorg Chem. 2024 Mar 18;63(11):5235-5245. doi: 10.1021/acs.inorgchem.4c00321.
Jin Yang 1 Meng-Meng Wang 1 Dong-Ping Deng 1 Hai Lin 1 Yan Su 1 2 Chen-Xu Shao 1 Si-Hui Li 1 Zheng-Hong Yu 2 Hong-Ke Liu 1 Zhi Su 1
Affiliations

Affiliations

  • 1 Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.
  • 2 Department of Rheumatology and Immunology, Jinling Hospital, Medical School of Nanjing University, Nanjing 210002, China.
Abstract

Cancer treatment has faced severe obstacles due to the smart biological system of Cancer cells. Herein, we report a three-in-one agent Ir-CA via attenuation of Cancer cell stemness with the down-regulated biomarker CD133 expression from the mitochondria-directed chemotherapy. Over 80% of Ir-CA could accumulate in mitochondria, result in severe mitochondrial dysfunctions, and subsequently initiate Mitophagy and cell cycle arrest to kill cisplatin-resistant A549R cells. In vitro and in vivo antimetastatic experiments demonstrated that Ir-CA can effectively inhibit metastasis with down-regulated MMP-2/MMP-9. RNA seq analysis and Western blotting indicated that Ir-CA also suppresses the GSTP1 expression to decrease the intracellular Pt-GS adducts, resulting in the detoxification and resensitization to cisplatin of A549R cells. In vivo evaluation indicated that Ir-CA restrains the tumor growth and has minimal side effects and superior biocompatibility. This work not only provides the first three-in-one agent to attenuate Cancer cell stemness and simultaneously realize Anticancer, antimetastasis, and conquer metallodrug resistance but also demonstrates the effectiveness of the mitochondria-directed strategy in Cancer treatment.

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