Targeting the Warburg Effect in Cancer: Where Do We Stand?

被引:77
作者
Barba, Ignasi [1 ,2 ]
Carrillo-Bosch, Laura [2 ]
Seoane, Joan [2 ,3 ]
机构
[1] Univ Vic, Cent Univ Catalonia, Fac Med, Vic 08500, Catalonia, Spain
[2] Univ Autonoma Barcelona, Vall dHebron Univ Hosp, Vall dHebron Inst Oncol VHIO, CIBERONC, Barcelona 08035, Spain
[3] Inst Catalana Recerca & Estudis Avancats ICREA, Barcelona 08010, Spain
关键词
tumor metabolism; tumor microenvironment; Warburg effect; aerobic glycolysis; immunomodulation; TUMOR-ASSOCIATED MACROPHAGES; LACTATE DEHYDROGENASE-A; AEROBIC GLYCOLYSIS; LUNG-CANCER; INHIBITION; CELLS; METABOLISM; 3-BROMOPYRUVATE; GLUCOSE; STRESS;
D O I
10.3390/ijms25063142
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
The Warburg effect, characterized by the preferential conversion of glucose to lactate even in the presence of oxygen and functional mitochondria, is a prominent metabolic hallmark of cancer cells and has emerged as a promising therapeutic target for cancer therapy. Elevated lactate levels and acidic pH within the tumor microenvironment (TME) resulting from glycolytic profoundly impact various cellular populations, including macrophage reprogramming and impairment of T-cell functionality. Altogether, the Warburg effect has been shown to promote tumor progression and immunosuppression through multiple mechanisms. This review provides an overview of the current understanding of the Warburg effect in cancer and its implications. We summarize recent pharmacological strategies aimed at targeting glycolytic enzymes, highlighting the challenges encountered in achieving therapeutic efficacy. Additionally, we examine the utility of the Warburg effect as an early diagnostic tool. Finally, we discuss the multifaceted roles of lactate within the TME, emphasizing its potential as a therapeutic target to disrupt metabolic interactions between tumor and immune cells, thereby enhancing anti-tumor immunity.
引用
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页数:17
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