氧化磷酸化
癌细胞
线粒体
癌症
糖酵解
酸中毒
生物
癌症研究
肿瘤微环境
代谢性酸中毒
瓦博格效应
代谢适应
细胞生物学
细胞
细胞呼吸
生物化学
适应(眼睛)
新陈代谢
化学
氧化应激
体内
细胞适应
转移
生物信息学
代谢途径
厌氧糖酵解
适应性反应
活性氧
作者
Bruna Martins Garcia,Patricia Altea‐Manzano
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2025-12-11
卷期号:86 (5): 1098-1100
标识
DOI:10.1158/0008-5472.can-25-5633
摘要
The tumor microenvironment imposes diverse metabolic challenges to cancer cells. Overcoming these challenges is essential for survival, proliferation, and dissemination. However, how cancer cells cope with the harsh environment and how the different coexisting stresses affect the tumor in vivo are unknown. Recently, Groessl and colleagues published their findings in Science showing that acidosis outweighs all other stresses and plays a major role in adaptation to them. Mechanistically, acidosis inhibits the ERK-dynamin-related protein 1 (DRP1) pathway, resulting in mitochondria elongation, which triggers a metabolic shift from glycolysis to oxidative phosphorylation (OXPHOS). These findings highlight the plasticity of cancer cell mitochondria and refute the previous belief that cancer mitochondria are inherently dysfunctional. Indeed, inhibition of mitochondrial fusion or OXPHOS in acidic tumors is sufficient to promote cell death. Thus, enhancing respiration under acidosis comes to light as an essential metabolic adaptation to cancer survival and proliferation, and targeting how cancer cells adapt to acidosis emerges as a new avenue for therapy.
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