Nuclear receptors as drug targets in metabolic diseases: new approaches to therapy

被引:50
|
作者
Tobin, James F.
Freedman, Leonard P.
机构
[1] Wyeth Ayerst Res, Dept Cardiovasc & Metab Dis, Cambridge, MA 02140 USA
[2] Wyeth Ayerst Res, Dept Womens Hlth & Musculoskeletal Biol, Collegeville, PA 19426 USA
来源
关键词
D O I
10.1016/j.tem.2006.07.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nuclear receptors represent novel targets for the development of therapeutic agents for the treatment of numerous diseases, including type 2 diabetes, obesity dyslipidemia, atherosclerosis and the metabolic syndrome. There have been many recent advances in the development of new therapeutic agents for a subset of these receptors, including the peroxisome proliferator-activated receptors, the liver X receptors and the farnesoid X receptor. To date, the synthesis of selective modulators that regulate the activity of these receptors has been empirical. However, a detailed understanding of the molecular basis for selective modulation, as well as new insights into the biology of these receptors, might open the door to the rational design of a new generation of therapeutic agents with improved safety and efficacy.
引用
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页码:284 / 290
页数:7
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