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Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment

Cancer cells preferentially utilize glycolysis, instead of oxidative phosphorylation, for metabolism even in the presence of oxygen. This phenomenon of aerobic glycolysis, referred to as the “Warburg effect”, commonly exists in a variety of tumors. Recent studies further demonstrate that both geneti...

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Detalles Bibliográficos
Autores principales: Justus, Calvin R., Sanderlin, Edward J., Yang, Li V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463690/
https://www.ncbi.nlm.nih.gov/pubmed/25988385
http://dx.doi.org/10.3390/ijms160511055
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author Justus, Calvin R.
Sanderlin, Edward J.
Yang, Li V.
author_facet Justus, Calvin R.
Sanderlin, Edward J.
Yang, Li V.
author_sort Justus, Calvin R.
collection PubMed
description Cancer cells preferentially utilize glycolysis, instead of oxidative phosphorylation, for metabolism even in the presence of oxygen. This phenomenon of aerobic glycolysis, referred to as the “Warburg effect”, commonly exists in a variety of tumors. Recent studies further demonstrate that both genetic factors such as oncogenes and tumor suppressors and microenvironmental factors such as spatial hypoxia and acidosis can regulate the glycolytic metabolism of cancer cells. Reciprocally, altered cancer cell metabolism can modulate the tumor microenvironment which plays important roles in cancer cell somatic evolution, metastasis, and therapeutic response. In this article, we review the progression of current understandings on the molecular interaction between cancer cell metabolism and the tumor microenvironment. In addition, we discuss the implications of these interactions in cancer therapy and chemoprevention.
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spelling pubmed-44636902015-06-16 Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment Justus, Calvin R. Sanderlin, Edward J. Yang, Li V. Int J Mol Sci Review Cancer cells preferentially utilize glycolysis, instead of oxidative phosphorylation, for metabolism even in the presence of oxygen. This phenomenon of aerobic glycolysis, referred to as the “Warburg effect”, commonly exists in a variety of tumors. Recent studies further demonstrate that both genetic factors such as oncogenes and tumor suppressors and microenvironmental factors such as spatial hypoxia and acidosis can regulate the glycolytic metabolism of cancer cells. Reciprocally, altered cancer cell metabolism can modulate the tumor microenvironment which plays important roles in cancer cell somatic evolution, metastasis, and therapeutic response. In this article, we review the progression of current understandings on the molecular interaction between cancer cell metabolism and the tumor microenvironment. In addition, we discuss the implications of these interactions in cancer therapy and chemoprevention. MDPI 2015-05-15 /pmc/articles/PMC4463690/ /pubmed/25988385 http://dx.doi.org/10.3390/ijms160511055 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Justus, Calvin R.
Sanderlin, Edward J.
Yang, Li V.
Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title_full Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title_fullStr Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title_full_unstemmed Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title_short Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment
title_sort molecular connections between cancer cell metabolism and the tumor microenvironment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463690/
https://www.ncbi.nlm.nih.gov/pubmed/25988385
http://dx.doi.org/10.3390/ijms160511055
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