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Metallomics insights into the programmed cell death induced by metal-based anticancer compounds
Cai-Ping Tan1, Yi-Ying Lu, Liang-Nian Ji
1MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275, P. R. China. cesmzw@mail.sysu.edu.cn.
Metal-based anticancer drugs can induce programmed cell death (PCD) through various pathways beyond apoptosis. This review explores metallomics studies on apoptosis, autophagy, and necroptosis, offering new cancer treatment strategies.
Area of Science:
- Biochemistry
- Pharmacology
- Oncology
Background:
- Metal-based anticancer agents, like cisplatin, have been researched for over 40 years.
- Apoptosis induction is a primary mechanism for metal-based cancer drugs, but resistance is common.
- Alternative cell death pathways are crucial for overcoming cancer resistance to apoptosis.
Purpose of the Study:
- To review metallomics studies on metal-induced cell death pathways.
- To highlight alternative programmed cell death (PCD) mechanisms beyond apoptosis.
- To discuss the potential of metal complexes targeting these alternative pathways for cancer therapy.
Main Methods:
- Review of recent metallomics studies.
- Analysis of metal-based drugs' mechanisms of action.
- Focus on three major PCD pathways: apoptosis, autophagy, and necroptosis.
Main Results:
- Metal complexes can induce cell death via non-apoptotic pathways.
- Autophagy and regulated necrosis (necroptosis) are significant alternative PCD routes.
- Metallomics provides insights into drug-target interactions and cell death induction.
Conclusions:
- Metal complexes offer diverse strategies for cancer treatment by targeting multiple cell death pathways.
- Understanding alternative PCD mechanisms is key to developing effective cancer therapies.
- Metallomics is essential for elucidating the action of novel metal-based anticancer drugs.
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