| Literature DB >> 24458094 |
Wenjing Zhang1, Yijun Gao1, Peixue Li1, Zhubing Shi1, Tong Guo1, Fei Li1, Xiangkun Han1, Yan Feng1, Chao Zheng1, Zuoyun Wang1, Fuming Li1, Haiquan Chen2, Zhaocai Zhou1, Lei Zhang1, Hongbin Ji1.
Abstract
Lung cancer is one of the most devastating diseases worldwide with high incidence and mortality. Hippo (Hpo) pathway is a conserved regulator of organ size in both Drosophila and mammals. Emerging evidence has suggested the significance of Hpo pathway in cancer development. In this study, we identify VGLL4 as a novel tumor suppressor in lung carcinogenesis through negatively regulating the formation of YAP-TEAD complex, the core component of Hpo pathway. Our data show that VGLL4 is frequently observed to be lowly expressed in both mouse and human lung cancer specimens. Ectopic expression of VGLL4 significantly suppresses the growth of lung cancer cells in vitro. More importantly, VGLL4 significantly inhibits lung cancer progression in de novo mouse model. We further find that VGLL4 inhibits the activity of the YAP-TEAD transcriptional complex. Our data show that VGLL4 directly competes with YAP in binding to TEADs and executes its growth-inhibitory function through two TDU domains. Collectively, our study demonstrates that VGLL4 is a novel tumor suppressor for lung cancer through negatively regulating the YAP-TEAD complex formation and thus the Hpo pathway.Entities:
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Year: 2014 PMID: 24458094 PMCID: PMC3945886 DOI: 10.1038/cr.2014.10
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617