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Fatty Acids and Breast Cancer: Make Them on Site or Have Them Delivered.
Kinlaw, William B; Baures, Paul W; Lupien, Leslie E; Davis, Wilson L; Kuemmerle, Nancy B.
Afiliação
  • Kinlaw WB; Division of Endocrinology and Metabolism, Department of Medicine, The Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, New Hampshire.
  • Baures PW; Department of Chemistry, Keene State University, Keene, New Hampshire.
  • Lupien LE; The Geisel School of Medicine at Dartmouth, Program in Experimental and Molecular Medicine, Lebanon, New Hampshire.
  • Davis WL; Division of Oncology, Department of Medicine, The Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire.
  • Kuemmerle NB; Division of Endocrinology and Metabolism, Department of Medicine, The Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, New Hampshire.
J Cell Physiol ; 231(10): 2128-41, 2016 10.
Article em En | MEDLINE | ID: mdl-26844415
ABSTRACT
Brisk fatty acid (FA) production by cancer cells is accommodated by the Warburg effect. Most breast and other cancer cell types are addicted to fatty acids (FA), which they require for membrane phospholipid synthesis, signaling purposes, and energy production. Expression of the enzymes required for FA synthesis is closely linked to each of the major classes of signaling molecules that stimulate BC cell proliferation. This review focuses on the regulation of FA synthesis in BC cells, and the impact of FA, or the lack thereof, on the tumor cell phenotype. Given growing awareness of the impact of dietary fat and obesity on BC biology, we will also examine the less-frequently considered notion that, in addition to de novo FA synthesis, the lipolytic uptake of preformed FA may also be an important mechanism of lipid acquisition. Indeed, it appears that cancer cells may exist at different points along a "lipogenic-lipolytic axis," and FA uptake could thwart attempts to exploit the strict requirement for FA focused solely on inhibition of de novo FA synthesis. Strategies for clinically targeting FA metabolism will be discussed, and the current status of the medicinal chemistry in this area will be assessed. J. Cell. Physiol. 231 2128-2141, 2016. © 2016 Wiley Periodicals, Inc.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proliferação de Células / Metabolismo dos Lipídeos / Lipogênese / Ácidos Graxos Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proliferação de Células / Metabolismo dos Lipídeos / Lipogênese / Ácidos Graxos Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article