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Cancer's sweet tooth for serine

Exemplified by the cancer cell's preference for glycolysis (the Warburg effect), altered metabolism has taken centerstage as an emerging hallmark of cancer. Charting the landscape of cancer metabolic addictions should reveal new avenues for therapeutic attack. Two recent studies found subsets o...

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Detalles Bibliográficos
Autor principal: Luo, Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315682/
https://www.ncbi.nlm.nih.gov/pubmed/22189202
http://dx.doi.org/10.1186/bcr2932
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author Luo, Ji
author_facet Luo, Ji
author_sort Luo, Ji
collection PubMed
description Exemplified by the cancer cell's preference for glycolysis (the Warburg effect), altered metabolism has taken centerstage as an emerging hallmark of cancer. Charting the landscape of cancer metabolic addictions should reveal new avenues for therapeutic attack. Two recent studies found subsets of human melanoma and breast cancers to have high levels of phosphoglycerate dehydrogenase (PHGDH), a key enzyme for serine biosynthesis, and these cancer cells are dependent on PHGDH for their growth and survival. Tumors may thus harbor distinct metabolic alterations to support their malignancy, and targeting enzymes such as PHGDH might prove a viable therapeutic strategy in this scenario.
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spelling pubmed-33156822012-05-28 Cancer's sweet tooth for serine Luo, Ji Breast Cancer Res Viewpoint Exemplified by the cancer cell's preference for glycolysis (the Warburg effect), altered metabolism has taken centerstage as an emerging hallmark of cancer. Charting the landscape of cancer metabolic addictions should reveal new avenues for therapeutic attack. Two recent studies found subsets of human melanoma and breast cancers to have high levels of phosphoglycerate dehydrogenase (PHGDH), a key enzyme for serine biosynthesis, and these cancer cells are dependent on PHGDH for their growth and survival. Tumors may thus harbor distinct metabolic alterations to support their malignancy, and targeting enzymes such as PHGDH might prove a viable therapeutic strategy in this scenario. BioMed Central 2011 2011-11-28 /pmc/articles/PMC3315682/ /pubmed/22189202 http://dx.doi.org/10.1186/bcr2932 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Viewpoint
Luo, Ji
Cancer's sweet tooth for serine
title Cancer's sweet tooth for serine
title_full Cancer's sweet tooth for serine
title_fullStr Cancer's sweet tooth for serine
title_full_unstemmed Cancer's sweet tooth for serine
title_short Cancer's sweet tooth for serine
title_sort cancer's sweet tooth for serine
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315682/
https://www.ncbi.nlm.nih.gov/pubmed/22189202
http://dx.doi.org/10.1186/bcr2932
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