| Literature DB >> 26522259 |
Rui Ju1, Lei Guo1, Juan Li1, Lei Zhu1, Xiaoli Yu1, Chen Chen1, Wei Chen1, Caiying Ye2, Dechang Zhang3.
Abstract
Targeting cancer cell metabolism is a promising strategy against cancer. Here, we confirmed that the anti-cancer drug carboxyamidotriazole (CAI) inhibited mitochondrial respiration in cancer cells for the first time and found a way to enhance its anti-cancer activity by further disturbing the energy metabolism. CAI promoted glucose uptake and lactate production when incubated with cancer cells. The oxidative phosphorylation (OXPHOS) in cancer cells was inhibited by CAI, and the decrease in the activity of the respiratory chain complex I could be one explanation. The anti-cancer effect of CAI was greatly potentiated when being combined with 2-deoxyglucose (2-DG). The cancer cells treated with the combination of CAI and 2-DG were arrested in G2/M phase. The apoptosis and necrosis rates were also increased. In a mouse xenograft model, this combination was well tolerated and retarded the tumor growth. The impairment of cancer cell survival was associated with significant cellular ATP decrease, suggesting that the combination of CAI and 2-DG could be one of the strategies to cause dual inhibition of energy pathways, which might be an effective therapeutic approach for a broad spectrum of tumors.Entities:
Keywords: 2-deoxyglucose; Carboxyamidotriazole; G2/M arrest; Glycolysis; Oxidative phosphorylation
Mesh:
Substances:
Year: 2015 PMID: 26522259 DOI: 10.1016/j.canlet.2015.10.025
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679