| Literature DB >> 29249695 |
Jonas Sieber1, Nicolas Wieder2, Abbe Clark2, Manuel Reitberger3, Sofia Matan3, Jeannine Schoenfelder3, Jianming Zhang3, Anna Mandinova3, Joshua Adam Bittker4, Juan Gutierrez4, Ozan Aygün4, Namrata Udeshi4, Steven Carr4, Peter Mundel3, Andreas Werner Jehle5, Anna Greka6.
Abstract
Progressive kidney diseases affect approximately 500 million people worldwide. Podocytes are terminally differentiated cells of the kidney filter, the loss of which leads to disease progression and kidney failure. To date, there are no therapies to promote podocyte survival. Drug repurposing may therefore help accelerate the development of cures in an area of tremendous unmet need. In a newly developed high-throughput screening assay of podocyte viability, we identified the BRAFV600E inhibitor GDC-0879 and the adenylate cyclase agonist forskolin as podocyte-survival-promoting compounds. GDC-0879 protects podocytes from injury through paradoxical activation of the MEK/ERK pathway. Forskolin promotes podocyte survival by attenuating protein biosynthesis. Importantly, GDC-0879 and forskolin are shown to promote podocyte survival against an array of cellular stressors. This work reveals new therapeutic targets for much needed podocyte-protective therapies and provides insights into the use of GDC-0879-like molecules for the treatment of progressive kidney diseases.Entities:
Keywords: BRAF; ER stress; ERK; MAPK; SB-682330; cell death; forskolin; glomerular disease; kidney disease; melanoma; post-mitotic cells
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Year: 2017 PMID: 29249695 PMCID: PMC5819995 DOI: 10.1016/j.chembiol.2017.11.006
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116