<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(12)</volume><submitter>Ali A</submitter><pubmed_abstract>Despite progress in genomic characterization, no single prognostic marker that can be evaluated using an easy-to-perform and relatively inexpensive method is available for pancreatic ductal adenocarcinoma (PDAC). MicroRNAs, which are stable, tumor- and tissue-specific molecules, are potentially ideal biomarkers, and we established an inter-laboratory validated method to investigate miR-21 as a prognostic biomarker in PDAC. The study samples of PDAC patients were recruited from a test cohort of Glasgow (n = 189) and three validation cohorts of Pisa (n = 69), Sydney (n = 249), and International Cancer Genome Consortium (ICGC) (n = 249). Tissue microarrays were used for miR-21 staining by chromogenic in situ hybridization (CISH). The patients were subdivided into no/low and high miR-21 staini</pubmed_abstract><journal>American journal of cancer research</journal><pagination>5668-5683</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9827095</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prognostic implications of microRNA-21 overexpression in pancreatic ductal adenocarcinoma: an international multicenter study of 686 patients.</pubmed_title><pmcid>PMC9827095</pmcid><pubmed_authors>Morton J</pubmed_authors><pubmed_authors>Duthie F</pubmed_authors><pubmed_authors>Giovannetti E</pubmed_authors><pubmed_authors>Oien KA</pubmed_authors><pubmed_authors>Funel N</pubmed_authors><pubmed_authors>Gill AJ</pubmed_authors><pubmed_authors>Khan IN</pubmed_authors><pubmed_authors>Frampton AE</pubmed_authors><pubmed_authors>Evans TRJ</pubmed_authors><pubmed_authors>McKay CJ</pubmed_authors><pubmed_authors>Samra J</pubmed_authors><pubmed_authors>Ali A</pubmed_authors><pubmed_authors>Chang D</pubmed_authors><pubmed_authors>Jamieson NB</pubmed_authors><pubmed_authors>Sansom O</pubmed_authors><pubmed_authors>Biankin A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic implications of microRNA-21 overexpression in pancreatic ductal adenocarcinoma: an international multicenter study of 686 patients.</name><description>Despite progress in genomic characterization, no single prognostic marker that can be evaluated using an easy-to-perform and relatively inexpensive method is available for pancreatic ductal adenocarcinoma (PDAC). MicroRNAs, which are stable, tumor- and tissue-specific molecules, are potentially ideal biomarkers, and we established an inter-laboratory validated method to investigate miR-21 as a prognostic biomarker in PDAC. The study samples of PDAC patients were recruited from a test cohort of Glasgow (n = 189) and three validation cohorts of Pisa (n = 69), Sydney (n = 249), and International Cancer Genome Consortium (ICGC) (n = 249). Tissue microarrays were used for miR-21 staining by chromogenic in situ hybridization (CISH). The patients were subdivided into no/low and high miR-21 staini</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T07:22:33.322Z</modification><creation>2025-04-04T07:22:33.322Z</creation></dates><accession>S-EPMC9827095</accession><cross_references><pubmed>36628279</pubmed></cross_references></HashMap>