肿瘤微环境
癌症
癌变
癌细胞
癌症研究
血管生成
肿瘤进展
转移
瓦博格效应
谷氨酰胺
重编程
生物
化学
生物化学
细胞
肿瘤细胞
氨基酸
遗传学
作者
Ricardo Pérez-Tomás,Isabel Pérez-Guillén
出处
期刊:Cancers
[MDPI AG]
日期:2020-11-03
卷期号:12 (11): 3244-3244
被引量:127
标识
DOI:10.3390/cancers12113244
摘要
Cancer is a complex disease that includes the reprogramming of metabolic pathways by malignant proliferating cells, including those affecting the tumor microenvironment (TME). The “TME concept” was introduced in recognition of the roles played by factors other than tumor cells in cancer progression. In response to the hypoxic or semi-hypoxic characteristic of the TME, cancer cells generate a large amount of lactate via the metabolism of glucose and glutamine. Export of this newly generated lactate by the tumor cells together with H+ prevents intracellular acidification but acidifies the TME. In recent years, the importance of lactate and acidosis in carcinogenesis has gained increasing attention, including the role of lactate as a tumor-promoting metabolite. Here we review the existing literature on lactate metabolism in tumor cells and the ability of extracellular lactate to direct the metabolic reprogramming of those cells. Studies demonstrating the roles of lactate in biological processes that drive or sustain carcinogenesis (tumor promotion, angiogenesis, metastasis and tumor resistance) and lactate’s role as an immunosuppressor that contributes to tumor evasion are also considered. Finally, we consider recent therapeutic efforts using available drugs directed at and interfering with lactate production and transport in cancer treatment.
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