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Targeting Long Chain Acyl-CoA Synthetases for Cancer Therapy.
Rossi Sebastiano, Matteo; Konstantinidou, Georgia.
Afiliación
  • Rossi Sebastiano M; Institute of Pharmacology, University of Bern, 3010 Bern, Switzerland.
  • Konstantinidou G; Institute of Pharmacology, University of Bern, 3010 Bern, Switzerland. georgia.konstantinidou@pki.unibe.ch.
Int J Mol Sci ; 20(15)2019 Jul 24.
Article en En | MEDLINE | ID: mdl-31344914
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 ß-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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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Coenzima A Ligasas / Lípidos / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Coenzima A Ligasas / Lípidos / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Int J Mol Sci Año: 2019 Tipo del documento: Article País de afiliación: Suiza