| Literature DB >> 33472968 |
Ying Wei1, Wenting Dong2, Julia Jackson3, Tsung-Che Ho2, Claude Jourdan Le Saux2, Alexis Brumwell2, Xiaopeng Li4, Julia Klesney-Tait5, Max L Cohen2, Paul J Wolters2, Harold A Chapman1,6.
Abstract
We recently identified epigallocatechin gallate (EGCG), a trihydroxyphenolic compound, as a dual inhibitor of lysyl oxidase-like2 and transforming growth factor-β1 (TGFβ1) receptor kinase that when given orally to patients with idiopathic pulmonary fibrosis (IPF) reversed profibrotic biomarkers in their diagnostic biopsies. Here, we extend these findings to advanced pulmonary fibrosis using cultured precision-cut lung slices from explants of patients with IPF undergoing transplantation. During these experiments, we were surprised to discover that not only did EGCG attenuate TGFβ1 signalling and new collagen accumulation but also activated matrix metalloproteinase-dependent collagen I turnover, raising the possibility of slow fibrosis resolution with continued treatment. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: interstitial fibrosis
Mesh:
Substances:
Year: 2021 PMID: 33472968 PMCID: PMC8222054 DOI: 10.1136/thoraxjnl-2020-215745
Source DB: PubMed Journal: Thorax ISSN: 0040-6376 Impact factor: 9.102