Consolidating Organometallic Complex Ir-CA Empowers Mitochondria-Directed Chemotherapy against Resistant Cancer via Stemness and Metastasis Inhibition.
Jin YangMeng-Meng WangDong-Ping DengHai LinYan SuChen-Xu ShaoSi-Hui LiZheng-Hong YuHong-Ke LiuZhi SuPublished in: Inorganic chemistry (2024)
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.
Keyphrases
- cell cycle arrest
- cell death
- rna seq
- induced apoptosis
- stem cells
- protein kinase
- epithelial mesenchymal transition
- pi k akt
- reactive oxygen species
- poor prognosis
- randomized controlled trial
- single cell
- endoplasmic reticulum
- signaling pathway
- transcription factor
- radiation therapy
- oxidative stress
- systematic review
- locally advanced
- binding protein
- long non coding rna
- squamous cell carcinoma
- endoplasmic reticulum stress
- young adults
- south africa
- cancer stem cells
- cell migration
- papillary thyroid