Pharmacological Targeting of BET Bromodomains Inhibits Lens Fibrosis via Downregulation of MYC Expression
Author(s) -
Xiaoran Wang,
Bowen Wang,
Na Zhao,
Chenjie Wang,
Mi Huang,
Baoxin Chen,
Jieping Chen,
Yan Sun,
Lang Xiong,
Shan Huang,
Yizhi Liu
Publication year - 2019
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.19-27596
Subject(s) - downregulation and upregulation , fibronectin , epithelial–mesenchymal transition , gene knockdown , bromodomain , chemistry , cancer research , cell migration , microbiology and biotechnology , transforming growth factor , fibrosis , biology , cell , cell culture , pathology , medicine , extracellular matrix , histone , gene , biochemistry , genetics
Lens fibrosis involves aberrant growth, migration, and transforming growth factorβ (TGFβ)-induced epithelial-mesenchymal transition (EMT) of lens epithelial cells (LECs). In this study, we investigated the role of the bromo- and extra-terminal domain (BET) inhibitor in lens fibrotic disorder to identify drug-based therapies.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom