Hypoxia restores the acidosis-induced inhibition of cancer cell dissemination

Acidosis is a hallmark of the tumor microenvironment and has been linked to aggressive cancer behavior, characterized by increased migration, invasion, and metastasis. We herein demonstrate that short-term exposure (24-72 h) to acidic extracellular pH (pH<sub>e</sub> = 6.4) suppresses cell proliferation, metabolism, dissociation from tumor spheroids, and migration in vitro as well as extravasation in chick embryos and mice. Acidosis acutely inhibits motility by downregulating the activity of sodium-hydrogen exchanger isoform-1 (NHE1), which in turn suppresses phosphatidylinositol 3-kinase (PI3K)/Akt. PI3K/Akt inhibition blocks Yes-associated protein (YAP) translocation to the nucleus, reducing NHE1 and integrin-linked kinase (ILK) expression. The resulting reduction in NHE1-/ILK-dependent migration and ATP production is rescued by hypoxia across cell types. While certain cancer cells can adapt to long-term (>3 weeks) acidosis and acquire an aggressive phenotype, acidosis-induced adaptation is not universal and depends on the cell's ability to restrain reactive oxygen species overproduction via fatty acid oxidation.

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Publication Details

Journal
Cell Reports
Published
2026-02-01
DOI
https://doi.org/10.1016/j.celrep.2026.116970
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
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article

Hypoxia restores the acidosis-induced inhibition of cancer cell dissemination

Stavroula Sofou, Inês Godet, Avery Tran, Selma A. Serra et al.
Cell Reports
Cancer, Hypoxia, and Metabolism
article

Hypoxia restores the acidosis-induced inhibition of cancer cell dissemination

Stavroula Sofou, Inês Godet, Avery Tran, Selma A. Serra, Debanik Choudhury, Κωνσταντίνος Κωνσταντόπουλος, Ryan L Huizar, Alice Amitrano, Pol Picón-Pagès, Miguel A. Valverde, Konstantin Stoletov, Andrew J. Ewald, Vivek K. Bajpai, James V. McCann, Qinling Yuan, Chen-Ming Fan, Sangmoo Jeong, Norbert Valles, Sean X. Sun, Daniele M. Gilkes, John D. Lewis, Se Jong Lee, Bhawana Agarwal
article en

Abstract

Acidosis is a hallmark of the tumor microenvironment and has been linked to aggressive cancer behavior, characterized by increased migration, invasion, and metastasis. We herein demonstrate that short-term exposure (24-72 h) to acidic extracellular pH (pH<sub>e</sub> = 6.4) suppresses cell proliferation, metabolism, dissociation from tumor spheroids, and migration in vitro as well as extravasation in chick embryos and mice. Acidosis acutely inhibits motility by downregulating the activity of sodium-hydrogen exchanger isoform-1 (NHE1), which in turn suppresses phosphatidylinositol 3-kinase (PI3K)/Akt. PI3K/Akt inhibition blocks Yes-associated protein (YAP) translocation to the nucleus, reducing NHE1 and integrin-linked kinase (ILK) expression. The resulting reduction in NHE1-/ILK-dependent migration and ATP production is rescued by hypoxia across cell types. While certain cancer cells can adapt to long-term (>3 weeks) acidosis and acquire an aggressive phenotype, acidosis-induced adaptation is not universal and depends on the cell's ability to restrain reactive oxygen species overproduction via fatty acid oxidation.

Cell ReportsVol. 45(2)
Johns Hopkins University (US), University of Alberta (CA), Universitat Pompeu Fabra (ES), Carnegie Institution for Science (US), Johns Hopkins Medicine (US), Department of Embryology (US), Sidney Kimmel Comprehensive Cancer Center (US), University of Oklahoma Health Sciences Center (US), University of Oklahoma (US)
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Cancer, Hypoxia, and Metabolism
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