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Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy

The deregulation of cancer cell metabolic networks is now recognized as one of the hallmarks of cancer. Abnormal lipid synthesis and extracellular lipid uptake are advantageous modifications fueling the needs of uncontrolled cancer cell proliferation. Fatty acids are placed at the crossroads of anab...

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Autores principales: Rossi Sebastiano, Matteo, Konstantinidou, Georgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696099/
https://www.ncbi.nlm.nih.gov/pubmed/31344914
http://dx.doi.org/10.3390/ijms20153624
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author Rossi Sebastiano, Matteo
Konstantinidou, Georgia
author_facet Rossi Sebastiano, Matteo
Konstantinidou, Georgia
author_sort Rossi Sebastiano, Matteo
collection PubMed
description The deregulation of cancer cell metabolic networks is now recognized as one of the hallmarks of cancer. Abnormal lipid synthesis and extracellular lipid uptake are advantageous modifications fueling the needs of uncontrolled cancer cell proliferation. Fatty acids are placed at the crossroads of anabolic and catabolic pathways, as they are implicated in the synthesis of phospholipids and triacylglycerols, or they can undergo β-oxidation. Key players to these decisions are the long-chain acyl-CoA synthetases, which are enzymes that catalyze the activation of long-chain fatty acids of 12–22 carbons. Importantly, the long-chain acyl-CoA synthetases are deregulated in many types of tumors, providing a rationale for anti-tumor therapeutic opportunities. The purpose of this review is to summarize the last up-to-date findings regarding their role in cancer, and to discuss the related emerging tumor targeting opportunities.
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spelling pubmed-66960992019-09-05 Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy Rossi Sebastiano, Matteo Konstantinidou, Georgia Int J Mol Sci Review The deregulation of cancer cell metabolic networks is now recognized as one of the hallmarks of cancer. Abnormal lipid synthesis and extracellular lipid uptake are advantageous modifications fueling the needs of uncontrolled cancer cell proliferation. Fatty acids are placed at the crossroads of anabolic and catabolic pathways, as they are implicated in the synthesis of phospholipids and triacylglycerols, or they can undergo β-oxidation. Key players to these decisions are the long-chain acyl-CoA synthetases, which are enzymes that catalyze the activation of long-chain fatty acids of 12–22 carbons. Importantly, the long-chain acyl-CoA synthetases are deregulated in many types of tumors, providing a rationale for anti-tumor therapeutic opportunities. The purpose of this review is to summarize the last up-to-date findings regarding their role in cancer, and to discuss the related emerging tumor targeting opportunities. MDPI 2019-07-24 /pmc/articles/PMC6696099/ /pubmed/31344914 http://dx.doi.org/10.3390/ijms20153624 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rossi Sebastiano, Matteo
Konstantinidou, Georgia
Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title_full Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title_fullStr Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title_full_unstemmed Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title_short Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy
title_sort targeting long chain acyl-coa synthetases for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696099/
https://www.ncbi.nlm.nih.gov/pubmed/31344914
http://dx.doi.org/10.3390/ijms20153624
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