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Ether lipid generating enzyme AGPS alters the balance of structural and signaling lipids to fuel cancer pathogenicity.
Benjamin, Daniel I; Cozzo, Alyssa; Ji, Xiaodan; Roberts, Lindsay S; Louie, Sharon M; Mulvihill, Melinda M; Luo, Kunxin; Nomura, Daniel K.
Afiliación
  • Benjamin DI; Program in Metabolic Biology, Department of Nutritional Sciences and Toxicology, and Division of Cell and Developmental Biology, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720.
Proc Natl Acad Sci U S A ; 110(37): 14912-7, 2013 Sep 10.
Article en En | MEDLINE | ID: mdl-23980144
ABSTRACT
Aberrant lipid metabolism is an established hallmark of cancer cells. In particular, ether lipid levels have been shown to be elevated in tumors, but their specific function in cancer remains elusive. We show here that the metabolic enzyme alkylglyceronephosphate synthase (AGPS), a critical step in the synthesis of ether lipids, is up-regulated across multiple types of aggressive human cancer cells and primary tumors. We demonstrate that ablation of AGPS in cancer cells results in reduced cell survival, cancer aggressiveness, and tumor growth through altering the balance of ether lipid, fatty acid, eicosanoid, and fatty acid-derived glycerophospholipid metabolism, resulting in an overall reduction in the levels of several oncogenic signaling lipids. Taken together, our results reveal that AGPS, in addition to maintaining ether lipids, also controls cellular utilization of fatty acids, favoring the generation of signaling lipids necessary for promoting the aggressive features of cancer.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Transferasas Alquil y Aril / Metabolismo de los Lípidos / Neoplasias Límite: Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2013 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Transferasas Alquil y Aril / Metabolismo de los Lípidos / Neoplasias Límite: Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2013 Tipo del documento: Article