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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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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. |
format | Online Article Text |
id | pubmed-3315682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT luoji cancerssweettoothforserine |