Targeting cancer and immune cell metabolism with the complex I inhibitors metformin and IACS-010759

被引:10
|
作者
Pujalte-Martin, Marc [1 ,2 ,3 ]
Belaid, Amine [1 ,2 ,3 ]
Bost, Simon [2 ,3 ]
Kahi, Michel [1 ,2 ,3 ]
Peraldi, Pascal [1 ,2 ,3 ]
Rouleau, Matthieu [2 ,3 ,4 ]
Mazure, Nathalie M. [1 ,2 ,3 ]
Bost, Frederic [1 ,2 ,3 ]
机构
[1] Ctr Mediterraneen Med Mol C3M, Inserm U1065, 151 Route St Antoine Ginestiere, F-06200 Nice, France
[2] Equipe Labellisee Ligue Natl Contre Canc, Paris, France
[3] Univ Cote Azur, Fac Med, Nice, France
[4] CNRS, LP2M, UMR7370, Nice, France
关键词
cancer; clinical trial; IACS-010759; immunometabolism; metformin; microenvironment; RANDOMIZED PHASE-II; PROSTATE-CANCER; OXIDATIVE-PHOSPHORYLATION; BREAST-CANCER; PANCREATIC-CANCER; MYELOID-LEUKEMIA; DOUBLE-BLIND; OPEN-LABEL; CHEMOTHERAPY; THERAPY;
D O I
10.1002/1878-0261.13583
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metformin and IACS-010759 are two distinct antimetabolic agents. Metformin, an established antidiabetic drug, mildly inhibits mitochondrial complex I, while IACS-010759 is a new potent mitochondrial complex I inhibitor. Mitochondria is pivotal in the energy metabolism of cells by providing adenosine triphosphate through oxidative phosphorylation (OXPHOS). Hence, mitochondrial metabolism and OXPHOS become a vulnerability when targeted in cancer cells. Both drugs have promising antitumoral effects in diverse cancers, supported by preclinical in vitro and in vivo studies. We present evidence of their direct impact on cancer cells and their immunomodulatory effects. In clinical studies, while observational epidemiologic studies on metformin were encouraging, actual trial results were not as expected. However, IACS-01075 exhibited major adverse effects, thereby causing a metabolic shift to glycolysis and elevated lactic acid concentrations. Therefore, the future outlook for these two drugs depends on preventive clinical trials for metformin and investigations into the plausible toxic effects on normal cells for IACS-01075. Metformin, an established antidiabetic drug, mildly inhibits mitochondrial complex I, while IACS-010759 is a potent complex I inhibitor. Both target cancer cells' vulnerability by impacting mitochondrial metabolism and oxidative phosphorylation. Promising preclinical results support their antitumoral effects. Clinical studies show metformin's mixed outcomes and IACS-01075's adverse effects. Prospects hinge on preventive metformin trials and investigations into IACS-01075's toxic effects on normal cells.image
引用
收藏
页码:1719 / 1738
页数:20
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