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dc.contributor.authorO'Mahony, Fiach C.
dc.contributor.authorFaratian, Dana
dc.contributor.authorVarley, James
dc.contributor.authorNanda, Jyoti
dc.contributor.authorTheodoulou, Marianna
dc.contributor.authorRiddick, Antony C. P.
dc.contributor.authorHarrison, David J.
dc.contributor.authorStewart, Grant D.
dc.date.accessioned2013-11-04T12:31:05Z
dc.date.available2013-11-04T12:31:05Z
dc.date.issued2012-02-21
dc.identifier.citationO'Mahony , F C , Faratian , D , Varley , J , Nanda , J , Theodoulou , M , Riddick , A C P , Harrison , D J & Stewart , G D 2012 , ' The use of automated quantitative analysis to evaluate epithelial-to-mesenchymal transition associated proteins in clear cell renal cell carcinoma ' , PLoS ONE , vol. 7 , no. 2 , e31557 . https://doi.org/10.1371/journal.pone.0031557en
dc.identifier.issn1932-6203
dc.identifier.otherPURE: 23158530
dc.identifier.otherPURE UUID: 806ad048-a735-41b7-8781-53eb58deb06e
dc.identifier.otherWOS: 000302873700070
dc.identifier.otherScopus: 84857428218
dc.identifier.otherORCID: /0000-0001-9041-9988/work/64034195
dc.identifier.urihttps://hdl.handle.net/10023/4148
dc.description.abstractBackground: Epithelial-to-mesenchymal transition (EMT) has recently been implicated in the initiation and progression of renal cell carcinoma (RCC). Some mRNA gene expression studies have suggested a link between the EMT phenotype and poorer clinical outcome from RCC. This study evaluated expression of EMT-associated proteins in RCC using in situ automated quantitative analysis immunofluorescence (AQUA) and compared expression levels with clinical outcome. Methods/Principal Findings: Unsupervised hierarchical cluster analysis of pre-existing RCC gene expression array data (GSE16449) from 36 patients revealed the presence of an EMT transcriptional signature in RCC [E-cadherin high/SLUG low/SNAIL low]. As automated immunofluorescence technology is dependent on accurate definition of the tumour cells in which measurements take place is critical, extensive optimisation was carried out resulting in a novel pan-cadherin based tumour mask that distinguishes renal cancer cells from stromal components. 61 patients with ccRCC and clinical follow-up were subsequently assessed for expression of EMT-associated proteins (WT1, SNAIL, SLUG, E-cadherin and phospho-beta-catenin) on tissue microarrays. Using Kaplan-Meier analysis both SLUG (p = 0.029) and SNAIL (p = 0.024) (log rank Mantel-Cox) were significantly associated with prolonged progression free survival (PFS). Using Cox regression univariate and multivariate analysis none of the biomarkers were significantly correlated with outcome. 14 of the 61 patients expressed the gene expression analysis predicted EMT-protein signature [E-cadherin high/SLUG low/SNAIL low], which was not found to be associated to PFS when measured at the protein level. A combination of high expression of SNAIL and low stage was able to stratify patients with greater significance (p = 0.001) then either variable alone (high SNAIL p = 0.024, low stage p = 0.029). Conclusions: AQUA has been shown to have the potential to identify EMT related protein targets in RCC allowing for stratification of patients into high and low risk groups, as well the ability to assess the association of reputed EMT signatures to progression of the disease.
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofPLoS ONEen
dc.rights© 2012 O'Mahony et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectEpithelial-to-mesenchymal transition (EMT)en
dc.subjectRenal cell carcinoma (RCC)en
dc.subjectmRNA gene expressionen
dc.subjectAutomated quantitative analysis immunofluorescence (AQUA)en
dc.subjectR Medicineen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccRen
dc.titleThe use of automated quantitative analysis to evaluate epithelial-to-mesenchymal transition associated proteins in clear cell renal cell carcinomaen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0031557
dc.description.statusPeer revieweden


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