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dc.contributor.authorStrauss, Philipp
dc.contributor.authorMarti, Hans-Peter
dc.contributor.authorBeisland, Christian
dc.contributor.authorScherer, Andreas
dc.contributor.authorLysne, Vegard
dc.contributor.authorLeh, Sabine Maria
dc.contributor.authorFlatberg, Arnar
dc.contributor.authorKoch, Even Evjen
dc.contributor.authorBeisvag, Vidar
dc.contributor.authorLandolt, Lea Zoe
dc.contributor.authorSkogstrand, Trude
dc.contributor.authorEikrem, Øystein Solberg
dc.date.accessioned2019-02-18T08:49:22Z
dc.date.available2019-02-18T08:49:22Z
dc.date.created2018-06-10T14:34:00Z
dc.date.issued2018
dc.identifier.citationInternational Journal of Molecular Sciences. 2018, 19:803 (3), 1-18.nb_NO
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/11250/2585820
dc.description.abstractNovel predictive tools for clear cell renal cell carcinoma (ccRCC) are urgently needed. MicroRNAs (miRNAs) have been increasingly investigated for their predictive value, and formalin-fixed paraffin-embedded biopsy archives may potentially be a valuable source of miRNA sequencing material, as they remain an underused resource. Core biopsies of both cancerous and adjacent normal tissues were obtained from patients (n = 12) undergoing nephrectomy. After small RNA-seq, several analyses were performed, including classifier evaluation, obesity-related inquiries, survival analysis using publicly available datasets, comparisons to the current literature and ingenuity pathway analyses. In a comparison of tumour vs. normal, 182 miRNAs were found with significant differential expression; miR-155 was of particular interest as it classified all ccRCC samples correctly and correlated well with tumour size (R2 = 0.83); miR-155 also predicted poor survival with hazard ratios of 2.58 and 1.81 in two different TCGA (The Cancer Genome Atlas) datasets in a univariate model. However, in a multivariate Cox regression analysis including age, sex, cancer stage and histological grade, miR-155 was not a statistically significant survival predictor. In conclusion, formalin-fixed paraffin-embedded biopsy tissues are a viable source of miRNA-sequencing material. Our results further support a role for miR-155 as a promising cancer classifier and potentially as a therapeutic target in ccRCC that merits further investigation.nb_NO
dc.language.isoengnb_NO
dc.publisherMDPInb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleExpanding the utilization of formalin-fixed, paraffin-embedded archives: Feasibility of miR-Seq for disease exploration and biomarker development from biopsies with clear cell renal cell Carcinomanb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1-18nb_NO
dc.source.volume19:803nb_NO
dc.source.journalInternational Journal of Molecular Sciencesnb_NO
dc.source.issue3nb_NO
dc.identifier.doi10.3390/ijms19030803
dc.identifier.cristin1590269
dc.description.localcode© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal