Journal article
Prevention of bleomycin-induced pulmonary fibrosis by a novel antifibrotic peptide with relaxin-like activity
A Pini, R Shemesh, CS Samuel, RAD Bathgate, A Zauberman, C Hermesh, A Wool, D Bani, G Rotman
Journal of Pharmacology and Experimental Therapeutics | Published : 2010
Abstract
Pulmonary fibrosis is a progressive and lethal lung disease characterized by accumulation of extracellular matrix and loss of pulmonary function. No cure exists for this pathologic condition, and current treatments often fail to slow its progression or relieve its symptoms. Relaxin was previously shown to induce a matrix-degrading phenotype in human lung fibroblasts in vitro and to inhibit pulmonary fibrosis in vivo. A novel peptide that targets the relaxin RXFP1/LGR7 receptor was recently identified using our computational platform designed to predict novel G protein-coupled receptor peptide agonists. In this study, we examined the antifibrotic properties of this novel peptide, designated C..
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Grants
Awarded by National Health and Medical Research Council of Australia
Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work was supported by the National Heart Foundation of Australia and National Health and Medical Research Council of Australia [R. D. Wright Fellowship 454636] (to C.S.S.); and the National Health and Medical Research Council [Senior Research Fellowship App ID: 509011] (to R.A.D.B.).