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Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia

Changes in cell metabolism and metabolic adaptation are hallmark features of many cancers, including leukemia, that support biological processes involved into tumor initiation, growth, and response to therapeutics. The discovery of mutations in key metabolic enzymes has highlighted the importance of...

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Detalles Bibliográficos
Autores principales: Stuani, Lucille, Sabatier, Marie, Sarry, Jean-Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637566/
https://www.ncbi.nlm.nih.gov/pubmed/31319822
http://dx.doi.org/10.1186/s12915-019-0670-4
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author Stuani, Lucille
Sabatier, Marie
Sarry, Jean-Emmanuel
author_facet Stuani, Lucille
Sabatier, Marie
Sarry, Jean-Emmanuel
author_sort Stuani, Lucille
collection PubMed
description Changes in cell metabolism and metabolic adaptation are hallmark features of many cancers, including leukemia, that support biological processes involved into tumor initiation, growth, and response to therapeutics. The discovery of mutations in key metabolic enzymes has highlighted the importance of metabolism in cancer biology and how these changes might constitute an Achilles heel for cancer treatment. In this Review, we discuss the role of metabolic and mitochondrial pathways dysregulated in acute myeloid leukemia, and the potential of therapeutic intervention targeting these metabolic dependencies on the proliferation, differentiation, stem cell function and cell survival to improve patient stratification and outcomes.
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spelling pubmed-66375662019-07-25 Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia Stuani, Lucille Sabatier, Marie Sarry, Jean-Emmanuel BMC Biol Review Changes in cell metabolism and metabolic adaptation are hallmark features of many cancers, including leukemia, that support biological processes involved into tumor initiation, growth, and response to therapeutics. The discovery of mutations in key metabolic enzymes has highlighted the importance of metabolism in cancer biology and how these changes might constitute an Achilles heel for cancer treatment. In this Review, we discuss the role of metabolic and mitochondrial pathways dysregulated in acute myeloid leukemia, and the potential of therapeutic intervention targeting these metabolic dependencies on the proliferation, differentiation, stem cell function and cell survival to improve patient stratification and outcomes. BioMed Central 2019-07-18 /pmc/articles/PMC6637566/ /pubmed/31319822 http://dx.doi.org/10.1186/s12915-019-0670-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Stuani, Lucille
Sabatier, Marie
Sarry, Jean-Emmanuel
Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title_full Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title_fullStr Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title_full_unstemmed Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title_short Exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
title_sort exploiting metabolic vulnerabilities for personalized therapy in acute myeloid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637566/
https://www.ncbi.nlm.nih.gov/pubmed/31319822
http://dx.doi.org/10.1186/s12915-019-0670-4
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