Mitochondria as a target of third row transition metal-based anticancer complexes

被引:24
|
作者
Olelewe, Chibuzor [1 ]
Awuah, Samuel G. [1 ,2 ,3 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[2] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA
[3] Univ Kentucky, Markey Canc Ctr, Lexington, KY 40536 USA
关键词
Mitochondria-targeting; Metal-based drugs; Metabolism; Platinum; Gold; Iridium; Rhenium; CYCLOMETALATED IRIDIUM(III) COMPLEXES; PHOTODYNAMIC ANTICANCER; CANCER-CELLS; METABOLISM; CISPLATIN; APOPTOSIS; PROTEIN; THERAPY; PATHWAY; GENOME;
D O I
10.1016/j.cbpa.2022.102235
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In pursuit of better treatment options for malignant tumors, metal-based complexes continue to show promise as attractive chemotherapeutics due to tunability, novel mechanisms, and potency exemplified by platinum agents. The metabolic character of tumors renders the mitochondria and other metabolism pathways fruitful targets for medicinal inorganic chemistry. Cumulative understanding of the role of mitochondria in tumorigenesis has ignited research in mitochondrial targeting metal-based complexes to overcome resistance and inhibit tumor growth with high potency and selectivity. Here, we discuss recent progress made in third row transition metal-based mitochondrial targeting agents with the goal of stimulating an active field of research toward new clinical anticancer agents and the elucidation of novel mechanisms of action.
引用
收藏
页数:9
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