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This version published online on September 17, 2009
Molecular Endocrinology, doi:10.1210/me.2009-0212
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Submitted on May 27, 2009
Accepted on July 24, 2009

Minireview: Nuclear Receptor-Controlled Steroid Hormone Synthesis and Metabolism

Jinhan He, Qiuqiong Cheng, and Wen Xie*

Center for Pharmacogenetics and Department of Pharmaceutical Sciences (J.H., Q.C., W.X.) and Department of Pharmacology & Chemical Biology (W.X.), University of Pittsburgh, Pittsburgh, Pennsylvania 15261

* To whom correspondence should be addressed. E-mail: wex6{at}pitt.edu.

Steroid hormones are essential in normal physiology whereas disruptions in hormonal homeostasis represent an important etiological factor for many human diseases. Steroid hormones exert most of their functions through the binding and activation of nuclear hormone receptors (NRs or NHRs), a superfamily of DNA-binding and often ligand-dependent transcription factors. In recent years, accumulating evidence has suggested that NRs can also regulate the biosynthesis and metabolism of steroid hormones. This review will focus on the recent progress in our understanding of the regulatory role of NRs in hormonal homeostasis and the implications of this regulation in physiology and diseases.

NURSA Molecule Pages Link:

Nuclear Receptors:   PPAR-α  |  PPARδ  |  PPAR-γ  |  LXR-β  |  LXR-α  |  FXR-α  |  VDR  |  PXR  |  ERR-α  |  ERR-β  |  ERR-γ  |  GR  |  SF-1  |  LRH-1
Ligands:   Corticosterone  |  Troglitazone  |  LGD 100268  |  T0901317  |  1  |  GW3965  |  Dexamethasone  |  17β-estradiol  |  Aldosterone






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