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PKM2, a Central Point of Regulation in Cancer Metabolism

Aerobic glycolysis is the dominant metabolic pathway utilized by cancer cells, owing to its ability to divert glucose metabolites from ATP production towards the synthesis of cellular building blocks (nucleotides, amino acids, and lipids) to meet the demands of proliferation. The M2 isoform of pyruv...

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Detalles Bibliográficos
Autores principales: Wong, Nicholas, De Melo, Jason, Tang, Damu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586519/
https://www.ncbi.nlm.nih.gov/pubmed/23476652
http://dx.doi.org/10.1155/2013/242513
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author Wong, Nicholas
De Melo, Jason
Tang, Damu
author_facet Wong, Nicholas
De Melo, Jason
Tang, Damu
author_sort Wong, Nicholas
collection PubMed
description Aerobic glycolysis is the dominant metabolic pathway utilized by cancer cells, owing to its ability to divert glucose metabolites from ATP production towards the synthesis of cellular building blocks (nucleotides, amino acids, and lipids) to meet the demands of proliferation. The M2 isoform of pyruvate kinase (PKM2) catalyzes the final and also a rate-limiting reaction in the glycolytic pathway. In the PK family, PKM2 is subjected to a complex regulation by both oncogenes and tumour suppressors, which allows for a fine-tone regulation of PKM2 activity. The less active form of PKM2 drives glucose through the route of aerobic glycolysis, while active PKM2 directs glucose towards oxidative metabolism. Additionally, PKM2 possesses protein tyrosine kinase activity and plays a role in modulating gene expression and thereby contributing to tumorigenesis. We will discuss our current understanding of PKM2's regulation and its many contributions to tumorigenesis.
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spelling pubmed-35865192013-03-09 PKM2, a Central Point of Regulation in Cancer Metabolism Wong, Nicholas De Melo, Jason Tang, Damu Int J Cell Biol Review Article Aerobic glycolysis is the dominant metabolic pathway utilized by cancer cells, owing to its ability to divert glucose metabolites from ATP production towards the synthesis of cellular building blocks (nucleotides, amino acids, and lipids) to meet the demands of proliferation. The M2 isoform of pyruvate kinase (PKM2) catalyzes the final and also a rate-limiting reaction in the glycolytic pathway. In the PK family, PKM2 is subjected to a complex regulation by both oncogenes and tumour suppressors, which allows for a fine-tone regulation of PKM2 activity. The less active form of PKM2 drives glucose through the route of aerobic glycolysis, while active PKM2 directs glucose towards oxidative metabolism. Additionally, PKM2 possesses protein tyrosine kinase activity and plays a role in modulating gene expression and thereby contributing to tumorigenesis. We will discuss our current understanding of PKM2's regulation and its many contributions to tumorigenesis. Hindawi Publishing Corporation 2013 2013-02-14 /pmc/articles/PMC3586519/ /pubmed/23476652 http://dx.doi.org/10.1155/2013/242513 Text en Copyright © 2013 Nicholas Wong et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Wong, Nicholas
De Melo, Jason
Tang, Damu
PKM2, a Central Point of Regulation in Cancer Metabolism
title PKM2, a Central Point of Regulation in Cancer Metabolism
title_full PKM2, a Central Point of Regulation in Cancer Metabolism
title_fullStr PKM2, a Central Point of Regulation in Cancer Metabolism
title_full_unstemmed PKM2, a Central Point of Regulation in Cancer Metabolism
title_short PKM2, a Central Point of Regulation in Cancer Metabolism
title_sort pkm2, a central point of regulation in cancer metabolism
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586519/
https://www.ncbi.nlm.nih.gov/pubmed/23476652
http://dx.doi.org/10.1155/2013/242513
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