The Sour Regulation of Metabolism: Acidity Challenges Tumor Cells While Fueling Their Metabolic Survival

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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Publication Details

Journal
Cancer Research
Published
2025-12-11
DOI
https://doi.org/10.1158/0008-5472.can-25-5633
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
0.00
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article

The Sour Regulation of Metabolism: Acidity Challenges Tumor Cells While Fueling Their Metabolic Survival

Patricia Altea‐Manzano, Bruna Martins Garcia
Cancer Research
Cancer, Hypoxia, and Metabolism
article

The Sour Regulation of Metabolism: Acidity Challenges Tumor Cells While Fueling Their Metabolic Survival

Patricia Altea‐Manzano, Bruna Martins Garcia
article en

Abstract

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.

Cancer ResearchVol. 86(5)
Centro Andaluz de Biología Molecular y Medicina Regenerativa (ES)
Openalex Percentile: Top 52%
Cancer, Hypoxia, and Metabolism
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