Best Practice & Research Clinical Endocrinology & Metabolism
Volume 21, Issue 2 , Pages 193-208, June 2007

New insights into thyroid hormone action

  • Paul M. Yen (Associate Professor)

      Affiliations

    • Corresponding Author InformationCorresponding author. Endocrinology Division, Department of Medicine, John Hopkins Bayview Medical Center, 5200 Eastern Avenue, Room 432, Baltimore, MD 21224, USA. Tel.: +1 410 550 1772; Fax: +1 410 550 6864.

Laboratory of Gene Regulation and Development, National Institute of Child Health and Development, National Institute of Health, Bethesda, MD, USA

Endocrinology Division, Department of Medicine, Johns Hopkins Bayview Medical Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA

Endocrinology Division, Department of Medicine, Johns Hopkins Bayview Medical Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA

Thyroid hormones (THs) have important effects on cellular development, growth, and metabolism. They bind to thyroid hormone receptors (TRs), TRα and TRβ, which belong to the nuclear hormone receptor superfamily. These receptors also bind to enhancer elements in the promoters of target genes, and can regulate both positive and negative transcription. Recent emerging evidence has characterized some of the molecular mechanisms by which THs regulate transcription as co-repressors, and co-activators have been identified and their effects on histone acetylation examined. THs also have rapid effects that do not require transcription. These can occur via TRs or other cellular proteins, and typically occur outside the nucleus. It appears that THs regulate multiple cellular functions using a diverse array of receptors and signaling systems. TR isoform- or pathway-specific drugs might provide the therapeutic benefits of TH action such as decreasing obesity or lowering cholesterol levels without some of the side effects of hyperthyroidism.

Key words: non-genomic, nuclear hormone receptor, thyroid hormone receptor, thyroid hormone, transcription

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PII: S1521-690X(07)00034-6

doi:10.1016/j.beem.2007.04.004

Best Practice & Research Clinical Endocrinology & Metabolism
Volume 21, Issue 2 , Pages 193-208, June 2007