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The Warburg effect and drug resistance

The Warburg effect describes the increased utilization of glycolysis rather than oxidative phosphorylation by tumour cells for their energy requirements under physiological oxygen conditions. This effect has been the basis for much speculation on the survival advantage of tumour cells, tumourigenesi...

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Detalles Bibliográficos
Autores principales: Bhattacharya, Bhaskar, Mohd Omar, Mohd Feroz, Soong, Richie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793921/
https://www.ncbi.nlm.nih.gov/pubmed/26750865
http://dx.doi.org/10.1111/bph.13422
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author Bhattacharya, Bhaskar
Mohd Omar, Mohd Feroz
Soong, Richie
author_facet Bhattacharya, Bhaskar
Mohd Omar, Mohd Feroz
Soong, Richie
author_sort Bhattacharya, Bhaskar
collection PubMed
description The Warburg effect describes the increased utilization of glycolysis rather than oxidative phosphorylation by tumour cells for their energy requirements under physiological oxygen conditions. This effect has been the basis for much speculation on the survival advantage of tumour cells, tumourigenesis and the microenvironment of tumours. More recently, studies have begun to reveal how the Warburg effect could influence drug efficacy and how our understanding of tumour energetics could be exploited to improve drug development. In particular, evidence is emerging demonstrating how better modelling of the tumour metabolic microenvironment could lead to a better prediction of drug efficacy and the identification of new combination strategies. This review will provide details of the current understanding of the complex interplay between glucose metabolism and pharmacology and discuss opportunities for utilizing the Warburg effect in future drug development.
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spelling pubmed-47939212016-04-08 The Warburg effect and drug resistance Bhattacharya, Bhaskar Mohd Omar, Mohd Feroz Soong, Richie Br J Pharmacol Review Articles The Warburg effect describes the increased utilization of glycolysis rather than oxidative phosphorylation by tumour cells for their energy requirements under physiological oxygen conditions. This effect has been the basis for much speculation on the survival advantage of tumour cells, tumourigenesis and the microenvironment of tumours. More recently, studies have begun to reveal how the Warburg effect could influence drug efficacy and how our understanding of tumour energetics could be exploited to improve drug development. In particular, evidence is emerging demonstrating how better modelling of the tumour metabolic microenvironment could lead to a better prediction of drug efficacy and the identification of new combination strategies. This review will provide details of the current understanding of the complex interplay between glucose metabolism and pharmacology and discuss opportunities for utilizing the Warburg effect in future drug development. John Wiley and Sons Inc. 2016-02-18 2016-03 /pmc/articles/PMC4793921/ /pubmed/26750865 http://dx.doi.org/10.1111/bph.13422 Text en © 2016 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Bhattacharya, Bhaskar
Mohd Omar, Mohd Feroz
Soong, Richie
The Warburg effect and drug resistance
title The Warburg effect and drug resistance
title_full The Warburg effect and drug resistance
title_fullStr The Warburg effect and drug resistance
title_full_unstemmed The Warburg effect and drug resistance
title_short The Warburg effect and drug resistance
title_sort warburg effect and drug resistance
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793921/
https://www.ncbi.nlm.nih.gov/pubmed/26750865
http://dx.doi.org/10.1111/bph.13422
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