Please use this identifier to cite or link to this item: https://doi.org/10.1002/jcp.22435
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dc.titleThe hippo pathway in biological control and cancer development
dc.contributor.authorChan, S.W.
dc.contributor.authorLim, C.J.
dc.contributor.authorChen, L.
dc.contributor.authorChong, Y.F.
dc.contributor.authorHuang, C.
dc.contributor.authorSong, H.
dc.contributor.authorHong, W.
dc.date.accessioned2014-11-25T09:49:09Z
dc.date.available2014-11-25T09:49:09Z
dc.date.issued2011-04
dc.identifier.citationChan, S.W., Lim, C.J., Chen, L., Chong, Y.F., Huang, C., Song, H., Hong, W. (2011-04). The hippo pathway in biological control and cancer development. Journal of Cellular Physiology 226 (4) : 928-939. ScholarBank@NUS Repository. https://doi.org/10.1002/jcp.22435
dc.identifier.issn00219541
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/108696
dc.description.abstractThe Hippo pathway is an evolutionally conserved protein kinase cascade involved in regulating organ size in vivo and cell contact inhibition in vitro by governing cell proliferation and apoptosis. Deregulation of the Hippo pathway is linked to cancer development. Its first core kinase Warts was identified in Drosophila more than 15 years ago, but it gained much attention when other core components of the pathway were identified 8 years later. Major discoveries of the pathway were made during past several years. The core kinase components Hippo, Salvador, Warts, and Mats in the fly and Mst1/2, WW45, Lats1/2, and Mob1 in mammals phosphorylate and inactivate downstream transcriptional co-activators Yorkie in the fly, Yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ) in mammals, respectively. Phosphorylated Yorkie, YAP, and TAZ are sequestered in the cytoplasm by interaction with 14-3-3 proteins. Here we review recent progresses of this pathway by focusing on how these proteins communicate with each other and how loss of regulation results in cancers. © 2010 Wiley-Liss, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/jcp.22435
dc.sourceScopus
dc.typeReview
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1002/jcp.22435
dc.description.sourcetitleJournal of Cellular Physiology
dc.description.volume226
dc.description.issue4
dc.description.page928-939
dc.description.codenJCLLA
dc.identifier.isiut000287258800007
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