Please use this identifier to cite or link to this item: https://doi.org/10.3390/genes7090055
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dc.titleTargeting the Hippo signaling pathway for tissue regeneration and cancer therapy
dc.contributor.authorJuan, W.C
dc.contributor.authorHong, W
dc.date.accessioned2020-10-22T02:50:32Z
dc.date.available2020-10-22T02:50:32Z
dc.date.issued2016
dc.identifier.citationJuan, W.C, Hong, W (2016). Targeting the Hippo signaling pathway for tissue regeneration and cancer therapy. Genes 7 (9) : 55. ScholarBank@NUS Repository. https://doi.org/10.3390/genes7090055
dc.identifier.issn20734425
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178869
dc.description.abstractThe Hippo signaling pathway is a highly-conserved developmental pathway that plays an essential role in organ size control, tumor suppression, tissue regeneration and stem cell self-renewal. The YES-associated protein (YAP) and the transcriptional co-activator with PDZ-binding motif (TAZ) are two important transcriptional co-activators that are negatively regulated by the Hippo signaling pathway. By binding to transcription factors, especially the TEA domain transcription factors (TEADs), YAP and TAZ induce the expression of growth-promoting genes, which can promote organ regeneration after injury. Therefore, controlled activation of YAP and TAZ can be useful for regenerative medicine. However, aberrant activation of YAP and TAZ due to deregulation of the Hippo pathway or overexpression of YAP/TAZ and TEADs can promote cancer development. Hence, pharmacological inhibition of YAP and TAZ may be a useful approach to treat tumors with high YAP and/or TAZ activity. In this review, we present the mechanisms regulating the Hippo pathway, the role of the Hippo pathway in tissue repair and cancer, as well as a detailed analysis of the different strategies to target the Hippo signaling pathway and the genes regulated by YAP and TAZ for regenerative medicine and cancer therapy. © 2016 by the authors; licensee MDPI, Basel, Switzerland.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectG protein coupled receptor
dc.subjectmevalonic acid
dc.subjectmicroRNA
dc.subjectphosphotransferase
dc.subjecttankyrase inhibitor
dc.subjecttranscription factor
dc.subjecttranscriptional co activator with PDZ binding motif
dc.subjectunclassified drug
dc.subjectyes associated protein
dc.subjectadherens junction
dc.subjectcancer growth
dc.subjectcancer therapy
dc.subjectcell polarity
dc.subjectenzyme inhibition
dc.subjectgene control
dc.subjectgene expression
dc.subjectgene targeting
dc.subjectHippo signaling pathway
dc.subjecthuman
dc.subjectmechanotransduction
dc.subjectmolecular interaction
dc.subjectnonhuman
dc.subjectprotein domain
dc.subjectprotein expression
dc.subjectprotein function
dc.subjectprotein protein interaction
dc.subjectReview
dc.subjectsignal transduction
dc.subjecttight junction
dc.subjecttissue regeneration
dc.subjectWnt signaling pathway
dc.subjectWW domain
dc.typeReview
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi10.3390/genes7090055
dc.description.sourcetitleGenes
dc.description.volume7
dc.description.issue9
dc.description.page55
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