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Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems

Lactate accumulation and acidification in tumours are a cancer hallmark associated with the Warburg effect. Lactic acidosis correlates with cancer malignancy, and the benefit it offers to tumours has been the subject of numerous hypotheses. Strikingly, lactic acidosis enhances cancer cell survival t...

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Autores principales: Daverio, Zoé, Kolkman, Maxime, Perrier, Johan, Brunet, Lexane, Bendridi, Nadia, Sanglar, Corinne, Berger, Marie-Agnès, Panthu, Baptiste, Rautureau, Gilles J. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584866/
https://www.ncbi.nlm.nih.gov/pubmed/37853114
http://dx.doi.org/10.1038/s41598-023-44783-3
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author Daverio, Zoé
Kolkman, Maxime
Perrier, Johan
Brunet, Lexane
Bendridi, Nadia
Sanglar, Corinne
Berger, Marie-Agnès
Panthu, Baptiste
Rautureau, Gilles J. P.
author_facet Daverio, Zoé
Kolkman, Maxime
Perrier, Johan
Brunet, Lexane
Bendridi, Nadia
Sanglar, Corinne
Berger, Marie-Agnès
Panthu, Baptiste
Rautureau, Gilles J. P.
author_sort Daverio, Zoé
collection PubMed
description Lactate accumulation and acidification in tumours are a cancer hallmark associated with the Warburg effect. Lactic acidosis correlates with cancer malignancy, and the benefit it offers to tumours has been the subject of numerous hypotheses. Strikingly, lactic acidosis enhances cancer cell survival to environmental glucose depletion by repressing high-rate glycolysis and lactic fermentation, and promoting an oxidative metabolism involving reactivated respiration. We used real-time NMR to evaluate how cytosolic lactate accumulation up to 40 mM and acidification up to pH 6.5 individually impact glucose consumption, lactate production and pyruvate evolution in isolated cytosols. We used a reductive cell-free system (CFS) to specifically study cytosolic metabolism independently of other Warburg-regulatory mechanisms found in the cell. We assessed the impact of lactate and acidification on the Warburg metabolism of cancer cytosols, and whether this effect extended to different cytosolic phenotypes of lactic fermentation and cancer. We observed that moderate acidification, independently of lactate concentration, drastically reduces the glucose consumption rate and halts lactate production in different lactic fermentation phenotypes. In parallel, for Warburg-type CFS lactate supplementation induces pyruvate accumulation at control pH, and can maintain a higher cytosolic pyruvate pool at low pH. Altogether, we demonstrate that intracellular acidification accounts for the direct repression of lactic fermentation by the Warburg-associated lactic acidosis.
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spelling pubmed-105848662023-10-20 Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems Daverio, Zoé Kolkman, Maxime Perrier, Johan Brunet, Lexane Bendridi, Nadia Sanglar, Corinne Berger, Marie-Agnès Panthu, Baptiste Rautureau, Gilles J. P. Sci Rep Article Lactate accumulation and acidification in tumours are a cancer hallmark associated with the Warburg effect. Lactic acidosis correlates with cancer malignancy, and the benefit it offers to tumours has been the subject of numerous hypotheses. Strikingly, lactic acidosis enhances cancer cell survival to environmental glucose depletion by repressing high-rate glycolysis and lactic fermentation, and promoting an oxidative metabolism involving reactivated respiration. We used real-time NMR to evaluate how cytosolic lactate accumulation up to 40 mM and acidification up to pH 6.5 individually impact glucose consumption, lactate production and pyruvate evolution in isolated cytosols. We used a reductive cell-free system (CFS) to specifically study cytosolic metabolism independently of other Warburg-regulatory mechanisms found in the cell. We assessed the impact of lactate and acidification on the Warburg metabolism of cancer cytosols, and whether this effect extended to different cytosolic phenotypes of lactic fermentation and cancer. We observed that moderate acidification, independently of lactate concentration, drastically reduces the glucose consumption rate and halts lactate production in different lactic fermentation phenotypes. In parallel, for Warburg-type CFS lactate supplementation induces pyruvate accumulation at control pH, and can maintain a higher cytosolic pyruvate pool at low pH. Altogether, we demonstrate that intracellular acidification accounts for the direct repression of lactic fermentation by the Warburg-associated lactic acidosis. Nature Publishing Group UK 2023-10-18 /pmc/articles/PMC10584866/ /pubmed/37853114 http://dx.doi.org/10.1038/s41598-023-44783-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Daverio, Zoé
Kolkman, Maxime
Perrier, Johan
Brunet, Lexane
Bendridi, Nadia
Sanglar, Corinne
Berger, Marie-Agnès
Panthu, Baptiste
Rautureau, Gilles J. P.
Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title_full Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title_fullStr Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title_full_unstemmed Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title_short Warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time NMR on cell-free systems
title_sort warburg-associated acidification represses lactic fermentation independently of lactate, contribution from real-time nmr on cell-free systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584866/
https://www.ncbi.nlm.nih.gov/pubmed/37853114
http://dx.doi.org/10.1038/s41598-023-44783-3
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