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| Main Authors: | , , , , , , , , , , , , , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Journal of the American Chemical Society
2025
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/40977283/ |
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| _version_ | 1868266149514313729 |
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| author | Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong |
| author_facet | Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong |
| collection | PubMed - marine biology |
| contents | Marine Natural Product Chagosendine C Induces Cuproptosis in Colorectal Cancer Cells by Targeting FDX1. Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong Humans Colorectal Neoplasms Antineoplastic Agents Animals Mice Copper Biological Products Cell Proliferation Drug Screening Assays, Antitumor Cell Line, Tumor Molecular Structure Apoptosis Colorectal cancer (CRC) treatment is hampered by high recurrence rates and drug resistance. Cuproptosis, a copper-induced cell death mechanism, offers a new therapeutic approach. Here, we identified a marine natural product, chagosendine C (CHC), which kills tumor cells by increasing the intracellular copper ion concentration. CHC and related metal coordination homodimer alkaloids were rapidly synthesized and purified for further pharmacological study. , CHC significantly inhibited HCT116 and RKO CRC cell growth, induced G1 phase arrest and cell death, and overcame oxaliplatin resistance. , CHC suppressed colorectal tumor growth in mice at 40 mg/kg without obvious toxic effects. Mechanistically, CHC induces cuproptosis by targeting FDX1, increasing intracellular copper ions and ROS levels in tumor cells, and leading to cell death. Thus, CHC presents a novel CRC treatment strategy, showing strong antitumor activity and potential to overcome oxaliplatin resistance with promising clinical prospects. |
| format | Artículo científico |
| id | pubmed_40977283 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Journal of the American Chemical Society |
| record_format | pubmed |
| spellingShingle | Marine Natural Product Chagosendine C Induces Cuproptosis in Colorectal Cancer Cells by Targeting FDX1. Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong Humans Colorectal Neoplasms Antineoplastic Agents Animals Mice Copper Biological Products Cell Proliferation Drug Screening Assays, Antitumor Cell Line, Tumor Molecular Structure Apoptosis Marine Natural Product Chagosendine C Induces Cuproptosis in Colorectal Cancer Cells by Targeting FDX1. Tao, Xiaoyu Wang, Hongru Wang, Qun Wang, Chengji Shao, Chang-Wei Jin, Yang Yu, Dianping Hu, Hongmei Zhang, Qing Xu, Mengting Geng, Xiangxin Xu, Hanchi Li, Linyang Shen, Ruling Guo, Yue-Wei Li, Xu-Wen Liu, Sanhong Zhang, Weidong Humans Colorectal Neoplasms Antineoplastic Agents Animals Mice Copper Biological Products Cell Proliferation Drug Screening Assays, Antitumor Cell Line, Tumor Molecular Structure Apoptosis Colorectal cancer (CRC) treatment is hampered by high recurrence rates and drug resistance. Cuproptosis, a copper-induced cell death mechanism, offers a new therapeutic approach. Here, we identified a marine natural product, chagosendine C (CHC), which kills tumor cells by increasing the intracellular copper ion concentration. CHC and related metal coordination homodimer alkaloids were rapidly synthesized and purified for further pharmacological study. , CHC significantly inhibited HCT116 and RKO CRC cell growth, induced G1 phase arrest and cell death, and overcame oxaliplatin resistance. , CHC suppressed colorectal tumor growth in mice at 40 mg/kg without obvious toxic effects. Mechanistically, CHC induces cuproptosis by targeting FDX1, increasing intracellular copper ions and ROS levels in tumor cells, and leading to cell death. Thus, CHC presents a novel CRC treatment strategy, showing strong antitumor activity and potential to overcome oxaliplatin resistance with promising clinical prospects. |
| title | Marine Natural Product Chagosendine C Induces Cuproptosis in Colorectal Cancer Cells by Targeting FDX1. |
| topic | Humans Colorectal Neoplasms Antineoplastic Agents Animals Mice Copper Biological Products Cell Proliferation Drug Screening Assays, Antitumor Cell Line, Tumor Molecular Structure Apoptosis |
| url | https://pubmed.ncbi.nlm.nih.gov/40977283/ |