| Literature DB >> 31944822 |
Daniela M Santos1, Lorena Pantano2, Gina Pronzati1, Paula Grasberger1, Clemens K Probst1, Katharine E Black1, Jillian J Spinney1, Lida P Hariri1,3, Royale Nichols1, Yufei Lin2, Michael Bieler4, Peter Seither5, Paul Nicklin6, David Wyatt7, Andrew M Tager1, Benjamin D Medoff1.
Abstract
Idiopathic pulmonary fibrosis is a lung disease with limited therapeutic options that is characterized by pathological fibroblast activation and aberrant lung remodeling with scar formation. YAP (Yes-associated protein) is a transcriptional coactivator that mediates mechanical and biochemical signals controlling fibroblast activation. In this study, we developed a high-throughput small-molecule screen for YAP inhibitors in primary human lung fibroblasts. Multiple HMG-CoA (hydroxymethylglutaryl-coenzyme A) reductase inhibitors (statins) were found to inhibit YAP nuclear localization via induction of YAP phosphorylation, cytoplasmic retention, and degradation. We further show that the mevalonate pathway regulates YAP activation, and that simvastatin treatment reduces fibrosis markers in activated human lung fibroblasts and in the bleomycin mouse model of pulmonary fibrosis. Finally, we show that simvastatin modulates YAP in vivo in mouse lung fibroblasts. Our results highlight the potential of small-molecule screens for YAP inhibitors and provide a mechanism for the antifibrotic activity of statins in idiopathic pulmonary fibrosis.Entities:
Keywords: HMG-CoA reductase inhibitor; Hippo pathway; drug screening; fibroblast; idiopathic pulmonary fibrosis
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Year: 2020 PMID: 31944822 PMCID: PMC7110981 DOI: 10.1165/rcmb.2019-0296OC
Source DB: PubMed Journal: Am J Respir Cell Mol Biol ISSN: 1044-1549 Impact factor: 6.914