| Literature DB >> 26592798 |
Ajaybabu V Pobbati1, Xiao Han2, Alvin W Hung3, Seetoh Weiguang3, Nur Huda3, Guo-Ying Chen3, CongBao Kang3, Cheng San Brian Chia3, Xuelian Luo4, Wanjin Hong5, Anders Poulsen6.
Abstract
The human TEAD family of transcription factors (TEAD1-4) is required for YAP-mediated transcription in the Hippo pathway. Hyperactivation of TEAD's co-activator YAP contributes to tissue overgrowth and human cancers, suggesting that pharmacological interference of TEAD-YAP activity may be an effective strategy for anticancer therapy. Here we report the discovery of a central pocket in the YAP-binding domain (YBD) of TEAD that is targetable by small-molecule inhibitors. Our X-ray crystallography studies reveal that flufenamic acid, a non-steroidal anti-inflammatory drug (NSAID), binds to the central pocket of TEAD2 YBD. Our biochemical and functional analyses further demonstrate that binding of NSAIDs to TEAD inhibits TEAD-YAP-dependent transcription, cell migration, and proliferation, indicating that the central pocket is important for TEAD function. Therefore, our studies discover a novel way of targeting TEAD transcription factors and set the stage for therapeutic development of specific TEAD-YAP inhibitors against human cancers.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26592798 PMCID: PMC4660270 DOI: 10.1016/j.str.2015.09.009
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006