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Hopefully devoted to Q: targeting glutamine addiction in cancer
Altered cell metabolism enables tumours to sustain their increased energetic and biosynthetic needs. Although tumour metabolism has long been considered a promising discipline in the development of cancer therapeutics, the majority of work has focused on changes in glucose metabolism. However, the c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520092/ https://www.ncbi.nlm.nih.gov/pubmed/28441384 http://dx.doi.org/10.1038/bjc.2017.113 |
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author | Still, Emma R Yuneva, Mariia O |
author_facet | Still, Emma R Yuneva, Mariia O |
author_sort | Still, Emma R |
collection | PubMed |
description | Altered cell metabolism enables tumours to sustain their increased energetic and biosynthetic needs. Although tumour metabolism has long been considered a promising discipline in the development of cancer therapeutics, the majority of work has focused on changes in glucose metabolism. However, the complexity of cellular metabolism means that very rarely is an individual metabolite required for a single purpose, and thus understanding the overall metabolic requirements of tumours is vital. Over the past 30 years, increasing evidence has shown that many tumours require glutamine as well as glucose for their proliferation and survival. In this minireview, we explore the complexity of glutamine metabolism in tumour cells, discussing how the overall context of the tumour dictates the requirement for glutamine and how this can affect the design of effective therapeutic strategies. |
format | Online Article Text |
id | pubmed-5520092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55200922017-07-27 Hopefully devoted to Q: targeting glutamine addiction in cancer Still, Emma R Yuneva, Mariia O Br J Cancer Review Altered cell metabolism enables tumours to sustain their increased energetic and biosynthetic needs. Although tumour metabolism has long been considered a promising discipline in the development of cancer therapeutics, the majority of work has focused on changes in glucose metabolism. However, the complexity of cellular metabolism means that very rarely is an individual metabolite required for a single purpose, and thus understanding the overall metabolic requirements of tumours is vital. Over the past 30 years, increasing evidence has shown that many tumours require glutamine as well as glucose for their proliferation and survival. In this minireview, we explore the complexity of glutamine metabolism in tumour cells, discussing how the overall context of the tumour dictates the requirement for glutamine and how this can affect the design of effective therapeutic strategies. Nature Publishing Group 2017-05-23 2017-04-25 /pmc/articles/PMC5520092/ /pubmed/28441384 http://dx.doi.org/10.1038/bjc.2017.113 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Review Still, Emma R Yuneva, Mariia O Hopefully devoted to Q: targeting glutamine addiction in cancer |
title | Hopefully devoted to Q: targeting glutamine addiction in cancer |
title_full | Hopefully devoted to Q: targeting glutamine addiction in cancer |
title_fullStr | Hopefully devoted to Q: targeting glutamine addiction in cancer |
title_full_unstemmed | Hopefully devoted to Q: targeting glutamine addiction in cancer |
title_short | Hopefully devoted to Q: targeting glutamine addiction in cancer |
title_sort | hopefully devoted to q: targeting glutamine addiction in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520092/ https://www.ncbi.nlm.nih.gov/pubmed/28441384 http://dx.doi.org/10.1038/bjc.2017.113 |
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