Please use this identifier to cite or link to this item: https://doi.org/10.1002/jcb.22913
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dc.titlePRL-3 phosphatase and cancer metastasis
dc.contributor.authorAl-Aidaroos, A.Q.O.
dc.contributor.authorZeng, Q.
dc.date.accessioned2014-12-12T08:04:38Z
dc.date.available2014-12-12T08:04:38Z
dc.date.issued2010-12-01
dc.identifier.citationAl-Aidaroos, A.Q.O., Zeng, Q. (2010-12-01). PRL-3 phosphatase and cancer metastasis. Journal of Cellular Biochemistry 111 (5) : 1087-1098. ScholarBank@NUS Repository. https://doi.org/10.1002/jcb.22913
dc.identifier.issn07302312
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/117355
dc.description.abstractThe deregulated expression of members of the phosphatase of regenerating liver (PRL) family has been implicated in the metastatic progression of multiple human cancers. Importantly, PRL-1 and PRL-3 both possess the capacity to drive key steps in metastatic progression. Yet, little is known about the regulation and oncogenic mechanisms of this emerging class of dual-specificity phosphatases. This prospect article details the involvement of PRLs in the metastatic cascade, the regulatory mechanisms controlling PRL expression, and recent efforts in the characterization of PRL-modulated pathways and substrates using biochemical and high-throughput approaches. Current advances and future prospects in anti-cancer therapy targeting this family are also discussed. © 2010 Wiley-Liss, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/jcb.22913
dc.sourceScopus
dc.subjectcancer cell signaling
dc.subjectcancer metastasis
dc.subjectPRL-3 phosphatase
dc.typeReview
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi10.1002/jcb.22913
dc.description.sourcetitleJournal of Cellular Biochemistry
dc.description.volume111
dc.description.issue5
dc.description.page1087-1098
dc.description.codenJCEBD
dc.identifier.isiut000286017400004
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