Rexinoid Bexarotene Modulates Triglyceride but not Cholesterol Metabolism via Gene-Specific Permissivity of the RXR/LXR Heterodimer in the Liver
Author(s) -
Fanny Lalloyer,
Thomas Åskov Pedersen,
Barbara Gross,
Sophie Lestavel,
Saı̈d Yous,
Emmanuelle Vallez,
Jan-Ακε Gustafsson,
Susanne Mandrup,
Catherine Fiévet,
Bart Staels,
Anne Tailleux
Publication year - 2009
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.109.189506
Subject(s) - bexarotene , liver x receptor , retinoid x receptor , lipogenesis , chromatin immunoprecipitation , hypertriglyceridemia , biology , cholesterol , nuclear receptor , chemistry , endocrinology , medicine , triglyceride , lipid metabolism , biochemistry , transcription factor , gene expression , promoter , gene
Bexarotene (Targretin) is a clinically used antitumoral agent which exerts its action through binding to and activation of the retinoid-X-receptor (RXR). The most frequent side-effect of bexarotene administration is an increase in plasma triglycerides, an independent risk factor of cardiovascular disease. The molecular mechanism behind this hypertriglyceridemia remains poorly understood.
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