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Metabolic rewiring in melanoma

Oncogene-driven metabolic rewiring is an adaptation to low nutrient and oxygen conditions in the tumor microenvironment that enables cancer cells of diverse origin to hyperproliferate. Aerobic glycolysis and enhanced reliance on glutamine utilization are prime examples of such rewiring. However, tis...

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Autores principales: Ratnikov, Boris I., Scott, David A., Osterman, Andrei L., Smith, Jeffrey W., Ronai, Ze’ev A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140782/
https://www.ncbi.nlm.nih.gov/pubmed/27270434
http://dx.doi.org/10.1038/onc.2016.198
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author Ratnikov, Boris I.
Scott, David A.
Osterman, Andrei L.
Smith, Jeffrey W.
Ronai, Ze’ev A.
author_facet Ratnikov, Boris I.
Scott, David A.
Osterman, Andrei L.
Smith, Jeffrey W.
Ronai, Ze’ev A.
author_sort Ratnikov, Boris I.
collection PubMed
description Oncogene-driven metabolic rewiring is an adaptation to low nutrient and oxygen conditions in the tumor microenvironment that enables cancer cells of diverse origin to hyperproliferate. Aerobic glycolysis and enhanced reliance on glutamine utilization are prime examples of such rewiring. However, tissue of origin as well as specific genetic and epigenetic changes determines gene expression profiles underlying these metabolic alterations in specific cancers. In melanoma, activation of the MAPK pathway driven by mutant BRAF or NRAS is a primary cause of malignant transformation. Activity of the MAPK pathway, as well as other factors, such as HIF1α, Myc and MITF, are among those that control the balance between non-oxidative and oxidative branches of central carbon metabolism. Here, we discuss the nature of metabolic alterations that underlie melanoma development and affect its response to therapy.
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spelling pubmed-51407822017-01-13 Metabolic rewiring in melanoma Ratnikov, Boris I. Scott, David A. Osterman, Andrei L. Smith, Jeffrey W. Ronai, Ze’ev A. Oncogene Article Oncogene-driven metabolic rewiring is an adaptation to low nutrient and oxygen conditions in the tumor microenvironment that enables cancer cells of diverse origin to hyperproliferate. Aerobic glycolysis and enhanced reliance on glutamine utilization are prime examples of such rewiring. However, tissue of origin as well as specific genetic and epigenetic changes determines gene expression profiles underlying these metabolic alterations in specific cancers. In melanoma, activation of the MAPK pathway driven by mutant BRAF or NRAS is a primary cause of malignant transformation. Activity of the MAPK pathway, as well as other factors, such as HIF1α, Myc and MITF, are among those that control the balance between non-oxidative and oxidative branches of central carbon metabolism. Here, we discuss the nature of metabolic alterations that underlie melanoma development and affect its response to therapy. 2016-06-06 2017-01-12 /pmc/articles/PMC5140782/ /pubmed/27270434 http://dx.doi.org/10.1038/onc.2016.198 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ratnikov, Boris I.
Scott, David A.
Osterman, Andrei L.
Smith, Jeffrey W.
Ronai, Ze’ev A.
Metabolic rewiring in melanoma
title Metabolic rewiring in melanoma
title_full Metabolic rewiring in melanoma
title_fullStr Metabolic rewiring in melanoma
title_full_unstemmed Metabolic rewiring in melanoma
title_short Metabolic rewiring in melanoma
title_sort metabolic rewiring in melanoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5140782/
https://www.ncbi.nlm.nih.gov/pubmed/27270434
http://dx.doi.org/10.1038/onc.2016.198
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