Literature DB >> 18197785

Gene expression in pulmonary fibrosis.

Eileen Hsu1, Hidekata Yasuoka, Carol A Feghali-Bostwick.   

Abstract

Pulmonary fibrosis is a phenotype that results from a variety of conditions and is associated with significant morbidity and mortality. Ongoing research in the field is driven by the need for effective treatments for pulmonary fibrosis. In this review, we highlight mechanisms that regulate gene expression in pulmonary fibrosis at multiple levels. Potential pathogenic mechanisms involve genetic background and transcriptional, posttranscriptional, translational, posttranslational, and epigenetic mechanisms. Pulmonary fibrosis results from abnormal gene expression and regulation that arise from a combination of inherited/acquired genetic alterations and environmental triggers. Collectively, these alterations result in increased expression of extracellular matrix components such as collagen and fibronectin and in the observed fibrosis. Insights gained from mechanisms identified to induce and/or perpetuate fibrosis in the lung will yield new targets for the development of more effective therapies.

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Year:  2008        PMID: 18197785     DOI: 10.1615/critreveukargeneexpr.v18.i1.40

Source DB:  PubMed          Journal:  Crit Rev Eukaryot Gene Expr        ISSN: 1045-4403            Impact factor:   1.807


  3 in total

1.  Cross-Talk between Transforming Growth Factor-β and Periostin Can Be Targeted for Pulmonary Fibrosis.

Authors:  Yasuhiro Nanri; Satoshi Nunomura; Yasuhiro Terasaki; Tomohito Yoshihara; Yusuke Hirano; Yasuyuki Yokosaki; Yukie Yamaguchi; Carol Feghali-Bostwick; Keiichi Ajito; Shoichi Murakami; Simon J Conway; Kenji Izuhara
Journal:  Am J Respir Cell Mol Biol       Date:  2020-02       Impact factor: 6.914

2.  JunB contributes to Id2 repression and the epithelial-mesenchymal transition in response to transforming growth factor-β.

Authors:  Megan Gervasi; Anna Bianchi-Smiraglia; Michael Cummings; Qiao Zheng; Dan Wang; Song Liu; Andrei V Bakin
Journal:  J Cell Biol       Date:  2012-03-05       Impact factor: 10.539

3.  Therapeutic effects of C-28 methyl ester of 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid (CDDO-Me; bardoxolone methyl) on radiation-induced lung inflammation and fibrosis in mice.

Authors:  Yan-Yang Wang; Cui-Ying Zhang; Ya-Qiong Ma; Zhi-Xu He; Hong Zhe; Shu-Feng Zhou
Journal:  Drug Des Devel Ther       Date:  2015-06-22       Impact factor: 4.162

  3 in total

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