| Literature DB >> 26456820 |
Wenqi Wang1, Nan Li2, Xu Li2, My Kim Tran2, Xin Han2, Junjie Chen3.
Abstract
As the key effector in the Hippo pathway, YAP was identified as an oncoprotein whose expression is elevated in various human cancers. However, the development of potentially therapeutic compounds targeting YAP has been slow and limited. Here, we find that tankyrase inhibitors suppress YAP activity. This effect is mediated by anigomotin (AMOT) family proteins. Tankyrases associate with AMOT family proteins and promote their degradation through E3 ligase RNF146. By antagonizing tankyrase activity, tankyrase inhibitors stabilize AMOT family proteins, thereby suppressing YAP oncogenic functions. Together, our studies not only demonstrate the tankyrase-RNF146-AMOT axis as an upstream pathway regulating YAP but also reveal a therapeutic opportunity in targeting YAP for cancer treatment.Entities:
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Year: 2015 PMID: 26456820 PMCID: PMC4618173 DOI: 10.1016/j.celrep.2015.09.014
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423