Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/11803
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Liu, Kevin H | en |
dc.contributor.author | Huynh, Nhi | en |
dc.contributor.author | Patel, Oneel | en |
dc.contributor.author | Shulkes, Arthur | en |
dc.contributor.author | Baldwin, Graham S | en |
dc.contributor.author | He, Hong | en |
dc.date.accessioned | 2015-05-16T01:25:53Z | |
dc.date.available | 2015-05-16T01:25:53Z | |
dc.date.issued | 2013-06-26 | en |
dc.identifier.citation | Cancer Letters 2013; 340(1): 22-9 | en |
dc.identifier.govdoc | 23811286 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/11803 | en |
dc.description.abstract | P21 activated kinase 1 (PAK1) enhances colorectal cancer (CRC) progression by stimulating Wnt/β-catenin and Ras oncogene, which promote CRC survival via stimulation of hypoxia-inducible factor 1α (HIF-1α). The aim of this study was to assess the mechanism involved in the stimulation by PAK1 of CRC survival. PAK1 promoted CRC cell survival by up-regulation of HIF-1α. PAK1 was over-expressed and hyper-activated in tumors of ApcΔ(14/+) mice, which was correlated with over-expression of HIF-1α and β-catenin. Inhibition of PAK1 decreased tumor growth and the expression of HIF-1α and β-catenin in tumors of ApcΔ(14/+) mice, and suppressed xenograft tumor survival in SCID mice. These findings indicate that PAK1 stimulates CRC survival by up-regulation of HIF-1α. | en |
dc.language.iso | en | en |
dc.subject.other | CRC | en |
dc.subject.other | HIF-1α | en |
dc.subject.other | PAK1 | en |
dc.subject.other | β-Catenin | en |
dc.subject.other | Animals | en |
dc.subject.other | Cell Hypoxia | en |
dc.subject.other | Cell Survival | en |
dc.subject.other | Colorectal Neoplasms.enzymology.pathology.therapy | en |
dc.subject.other | Enzyme Activation | en |
dc.subject.other | Female | en |
dc.subject.other | Gene Expression Regulation, Neoplastic | en |
dc.subject.other | Gene Knockdown Techniques | en |
dc.subject.other | HCT116 Cells | en |
dc.subject.other | HT29 Cells | en |
dc.subject.other | Humans | en |
dc.subject.other | Hypoxia-Inducible Factor 1, alpha Subunit.genetics.metabolism | en |
dc.subject.other | Male | en |
dc.subject.other | Mice | en |
dc.subject.other | Mice, Inbred C57BL | en |
dc.subject.other | Mice, Knockout | en |
dc.subject.other | Mice, SCID | en |
dc.subject.other | RNA, Small Interfering.genetics | en |
dc.subject.other | Tumor Burden | en |
dc.subject.other | Up-Regulation | en |
dc.subject.other | Vascular Endothelial Growth Factor A.secretion | en |
dc.subject.other | beta Catenin.metabolism | en |
dc.subject.other | p21-Activated Kinases.antagonists & inhibitors.physiology | en |
dc.title | P21-activated kinase 1 promotes colorectal cancer survival by up-regulation of hypoxia-inducible factor-1α. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Cancer letters | en |
dc.identifier.affiliation | Department of Surgery, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia | en |
dc.identifier.doi | 10.1016/j.canlet.2013.06.024 | en |
dc.description.pages | 22-9 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/23811286 | en |
dc.type.austin | Journal Article | en |
local.name.researcher | He, Hong | |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Surgery (University of Melbourne) | - |
Appears in Collections: | Journal articles |
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.