Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11591
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dc.contributor.authorHe, Hongen
dc.contributor.authorBaldwin, Graham Sen
dc.date.accessioned2015-05-16T01:12:24Z
dc.date.available2015-05-16T01:12:24Z
dc.date.issued2012-10-22en
dc.identifier.citationBiochimica Et Biophysica Acta 2012; 1833(1): 33-9en
dc.identifier.govdoc23092728en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11591en
dc.description.abstractp21-activated kinases (PAKs) were initially identified as effector proteins downstream from GTPases of the Rho family. To date, six members of the PAK family have been discovered in mammalian cells. PAKs play important roles in growth factor signalling, cytoskeletal remodelling, gene transcription, cell proliferation and oncogenic transformation. A large body of research has demonstrated that PAKs are up-regulated in several human cancers, and that their overexpression is linked to tumour progression and resistance to therapy. Structural and biochemical studies have revealed the mechanisms involved in PAK signalling, and opened the way to the development of PAK-targeted therapies for cancer treatment. Here we summarise recent findings from biological and clinical research on the role of PAKs in gastrointestinal cancer, and discuss the current status of PAK-targeted anticancer therapies.en
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherCarcinoma.genetics.metabolismen
dc.subject.otherGastrointestinal Neoplasms.genetics.metabolismen
dc.subject.otherHumansen
dc.subject.otherModels, Biologicalen
dc.subject.otherMolecular Targeted Therapy.methods.trendsen
dc.subject.otherp21-Activated Kinases.chemistry.genetics.metabolism.physiologyen
dc.titlep21-activated kinases and gastrointestinal cancer.en
dc.typeJournal Articleen
dc.identifier.journaltitleBiochimica et biophysica actaen
dc.identifier.affiliationDepartment of Surgery, University of Melbourne, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1016/j.bbamcr.2012.10.015en
dc.description.pages33-9en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23092728en
dc.type.austinJournal Articleen
local.name.researcherHe, Hong
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptSurgery (University of Melbourne)-
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