Literature DB >> 18541529

Role of dual specificity phosphatases in biological responses to glucocorticoids.

Andrew R Clark1, Joana R S Martins, Carmen R Tchen.   

Abstract

The powerful anti-inflammatory effects of glucocorticoids (GCs) have been known for more than sixty years, but their molecular mechanisms are still incompletely understood and hotly debated. The GC receptor (GR) was cloned in 1985 and shown to be a transcription factor. Initially, the anti-inflammatory actions of GCs were explained in terms of genes that were up-regulated by the receptor. However, none of these putative mediators seemed able to account for the spectrum of anti-inflammatory responses to GCs. The discovery of a negative regulatory function of GR then shifted the focus away from GC-induced genes as anti-inflammatory mediators. In recent years, attention has begun to move back toward the idea that the anti-inflammatory response to GCs is partially dependent on the positive regulation of gene expression by GR.

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Year:  2008        PMID: 18541529      PMCID: PMC3258850          DOI: 10.1074/jbc.R700053200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  82 in total

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  38 in total

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7.  Progesterone and the Repression of Myometrial Inflammation: The Roles of MKP-1 and the AP-1 System.

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8.  Dual specificity phosphatase 1 regulates human inducible nitric oxide synthase expression by p38 MAP kinase.

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9.  Glucocorticoid regulation of mouse and human dual specificity phosphatase 1 (DUSP1) genes: unusual cis-acting elements and unexpected evolutionary divergence.

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Review 10.  Genomic and non-genomic effects of glucocorticoids: implications for breast cancer.

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