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Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters
SIMPLE SUMMARY: The “Warburg effect” refers to the situation wherein cellular energetics (ATP formation) use “aerobic glycolysis” (i.e., glucose use with the release of lactate (2 ATP per glucose)) even if oxygen present would authorize full oxidation with a much higher yield (34 ATP per glucose). T...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533123/ https://www.ncbi.nlm.nih.gov/pubmed/34681099 http://dx.doi.org/10.3390/biology10101000 |
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author | Bouillaud, Frédéric Hammad, Noureddine Schwartz, Laurent |
author_facet | Bouillaud, Frédéric Hammad, Noureddine Schwartz, Laurent |
author_sort | Bouillaud, Frédéric |
collection | PubMed |
description | SIMPLE SUMMARY: The “Warburg effect” refers to the situation wherein cellular energetics (ATP formation) use “aerobic glycolysis” (i.e., glucose use with the release of lactate (2 ATP per glucose)) even if oxygen present would authorize full oxidation with a much higher yield (34 ATP per glucose). The present article reviews possible reasons to explain this metabolic bias. ABSTRACT: Cellular bioenergetics requires an intense ATP turnover that is increased further by hypermetabolic states caused by cancer growth or inflammation. Both are associated with metabolic alterations and, notably, enhancement of the Warburg effect (also known as aerobic glycolysis) of poor efficiency with regard to glucose consumption when compared to mitochondrial respiration. Therefore, beside this efficiency issue, other properties of these two pathways should be considered to explain this paradox: (1) biosynthesis, for this only indirect effect should be considered, since lactate release competes with biosynthetic pathways in the use of glucose; (2) ATP production, although inefficient, glycolysis shows other advantages when compared to mitochondrial respiration and lactate release may therefore reflect that the glycolytic flux is higher than required to feed mitochondria with pyruvate and glycolytic NADH; (3) Oxygen supply becomes critical under hypermetabolic conditions, and the ATP/O(2) ratio quantifies the efficiency of oxygen use to regenerate ATP, although aerobic metabolism remains intense the participation of anaerobic metabolisms (lactic fermentation or succinate generation) could greatly increase ATP/O(2) ratio; (4) time and space constraints would explain that anaerobic metabolism is required while the general metabolism appears oxidative; and (5) active repression of respiration by glycolytic intermediates, which could ensure optimization of glucose and oxygen use. |
format | Online Article Text |
id | pubmed-8533123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85331232021-10-23 Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters Bouillaud, Frédéric Hammad, Noureddine Schwartz, Laurent Biology (Basel) Opinion SIMPLE SUMMARY: The “Warburg effect” refers to the situation wherein cellular energetics (ATP formation) use “aerobic glycolysis” (i.e., glucose use with the release of lactate (2 ATP per glucose)) even if oxygen present would authorize full oxidation with a much higher yield (34 ATP per glucose). The present article reviews possible reasons to explain this metabolic bias. ABSTRACT: Cellular bioenergetics requires an intense ATP turnover that is increased further by hypermetabolic states caused by cancer growth or inflammation. Both are associated with metabolic alterations and, notably, enhancement of the Warburg effect (also known as aerobic glycolysis) of poor efficiency with regard to glucose consumption when compared to mitochondrial respiration. Therefore, beside this efficiency issue, other properties of these two pathways should be considered to explain this paradox: (1) biosynthesis, for this only indirect effect should be considered, since lactate release competes with biosynthetic pathways in the use of glucose; (2) ATP production, although inefficient, glycolysis shows other advantages when compared to mitochondrial respiration and lactate release may therefore reflect that the glycolytic flux is higher than required to feed mitochondria with pyruvate and glycolytic NADH; (3) Oxygen supply becomes critical under hypermetabolic conditions, and the ATP/O(2) ratio quantifies the efficiency of oxygen use to regenerate ATP, although aerobic metabolism remains intense the participation of anaerobic metabolisms (lactic fermentation or succinate generation) could greatly increase ATP/O(2) ratio; (4) time and space constraints would explain that anaerobic metabolism is required while the general metabolism appears oxidative; and (5) active repression of respiration by glycolytic intermediates, which could ensure optimization of glucose and oxygen use. MDPI 2021-10-04 /pmc/articles/PMC8533123/ /pubmed/34681099 http://dx.doi.org/10.3390/biology10101000 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Opinion Bouillaud, Frédéric Hammad, Noureddine Schwartz, Laurent Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title | Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title_full | Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title_fullStr | Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title_full_unstemmed | Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title_short | Warburg Effect, Glutamine, Succinate, Alanine, When Oxygen Matters |
title_sort | warburg effect, glutamine, succinate, alanine, when oxygen matters |
topic | Opinion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533123/ https://www.ncbi.nlm.nih.gov/pubmed/34681099 http://dx.doi.org/10.3390/biology10101000 |
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