Targeting lactate metabolism for cancer therapeutics

被引:900
作者
Doherty, Joanne R. [1 ]
Cleveland, John L. [1 ]
机构
[1] Scripps Florida, Dept Canc Biol, Scripps Res Inst, Jupiter, FL USA
关键词
MONOCARBOXYLATE TRANSPORTER 1; TUMOR-STROMA COEVOLUTION; OXIDATIVE STRESS; LACTIC-ACID; AEROBIC GLYCOLYSIS; CELL-DEATH; PROMOTER HYPERMETHYLATION; TRANSCRIPTIONAL PROGRAM; MALIGNANT GLIOMA; PYRUVATE-KINASE;
D O I
10.1172/JCI69741
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Lactate, once considered a waste product of glycolysis, has emerged as a critical regulator of cancer development, maintenance, and metastasis. Indeed, tumor lactate levels correlate with increased metastasis, tumor recurrence, and poor outcome. Lactate mediates cancer cell intrinsic effects on metabolism and has additional non-tumor cell autonomous effects that drive tumorigenesis. Tumor cells can metabolize lactate as an energy source and shuttle lactate to neighboring cancer cells, adjacent stroma, and vascular endothelial cells, which induces metabolic reprogramming. Lactate also plays roles in promoting tumor inflammation and in functioning as a signaling molecule that stimulates tumor angiogenesis. Here we review the mechanisms of lactate production and transport and highlight emerging evidence indicating that targeting lactate metabolism is a promising approach for cancer therapeutics.
引用
收藏
页码:3685 / 3692
页数:8
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