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Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery

Recent studies have uncovered microRNAs (miRNAs) that have been overlooked in early genomic explorations, which show remarkable tissue- and context-specific expression. Here, we aim to identify and characterize previously unannotated miRNAs expressed in gastric adenocarcinoma (GA). Raw small RNA-seq...

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Autores principales: Pewarchuk, Michelle E., Barros-Filho, Mateus C., Minatel, Brenda C., Cohn, David E., Guisier, Florian, Sage, Adam P., Marshall, Erin A., Stewart, Greg L., Rock, Leigha D., Garnis, Cathie, Lam, Wan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6888638/
https://www.ncbi.nlm.nih.gov/pubmed/31739401
http://dx.doi.org/10.3390/ijms20225697
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author Pewarchuk, Michelle E.
Barros-Filho, Mateus C.
Minatel, Brenda C.
Cohn, David E.
Guisier, Florian
Sage, Adam P.
Marshall, Erin A.
Stewart, Greg L.
Rock, Leigha D.
Garnis, Cathie
Lam, Wan L.
author_facet Pewarchuk, Michelle E.
Barros-Filho, Mateus C.
Minatel, Brenda C.
Cohn, David E.
Guisier, Florian
Sage, Adam P.
Marshall, Erin A.
Stewart, Greg L.
Rock, Leigha D.
Garnis, Cathie
Lam, Wan L.
author_sort Pewarchuk, Michelle E.
collection PubMed
description Recent studies have uncovered microRNAs (miRNAs) that have been overlooked in early genomic explorations, which show remarkable tissue- and context-specific expression. Here, we aim to identify and characterize previously unannotated miRNAs expressed in gastric adenocarcinoma (GA). Raw small RNA-sequencing data were analyzed using the miRMaster platform to predict and quantify previously unannotated miRNAs. A discovery cohort of 475 gastric samples (434 GA and 41 adjacent nonmalignant samples), collected by The Cancer Genome Atlas (TCGA), were evaluated. Candidate miRNAs were similarly assessed in an independent cohort of 25 gastric samples. We discovered 170 previously unannotated miRNA candidates expressed in gastric tissues. The expression of these novel miRNAs was highly specific to the gastric samples, 143 of which were significantly deregulated between tumor and nonmalignant contexts (p-adjusted < 0.05; fold change > 1.5). Multivariate survival analyses showed that the combined expression of one previously annotated miRNA and two novel miRNA candidates was significantly predictive of patient outcome. Further, the expression of these three miRNAs was able to stratify patients into three distinct prognostic groups (p = 0.00003). These novel miRNAs were also present in the independent cohort (43 sequences detected in both cohorts). Our findings uncover novel miRNA transcripts in gastric tissues that may have implications in the biology and management of gastric adenocarcinoma.
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spelling pubmed-68886382019-12-09 Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery Pewarchuk, Michelle E. Barros-Filho, Mateus C. Minatel, Brenda C. Cohn, David E. Guisier, Florian Sage, Adam P. Marshall, Erin A. Stewart, Greg L. Rock, Leigha D. Garnis, Cathie Lam, Wan L. Int J Mol Sci Communication Recent studies have uncovered microRNAs (miRNAs) that have been overlooked in early genomic explorations, which show remarkable tissue- and context-specific expression. Here, we aim to identify and characterize previously unannotated miRNAs expressed in gastric adenocarcinoma (GA). Raw small RNA-sequencing data were analyzed using the miRMaster platform to predict and quantify previously unannotated miRNAs. A discovery cohort of 475 gastric samples (434 GA and 41 adjacent nonmalignant samples), collected by The Cancer Genome Atlas (TCGA), were evaluated. Candidate miRNAs were similarly assessed in an independent cohort of 25 gastric samples. We discovered 170 previously unannotated miRNA candidates expressed in gastric tissues. The expression of these novel miRNAs was highly specific to the gastric samples, 143 of which were significantly deregulated between tumor and nonmalignant contexts (p-adjusted < 0.05; fold change > 1.5). Multivariate survival analyses showed that the combined expression of one previously annotated miRNA and two novel miRNA candidates was significantly predictive of patient outcome. Further, the expression of these three miRNAs was able to stratify patients into three distinct prognostic groups (p = 0.00003). These novel miRNAs were also present in the independent cohort (43 sequences detected in both cohorts). Our findings uncover novel miRNA transcripts in gastric tissues that may have implications in the biology and management of gastric adenocarcinoma. MDPI 2019-11-14 /pmc/articles/PMC6888638/ /pubmed/31739401 http://dx.doi.org/10.3390/ijms20225697 Text en © 2019 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/).
spellingShingle Communication
Pewarchuk, Michelle E.
Barros-Filho, Mateus C.
Minatel, Brenda C.
Cohn, David E.
Guisier, Florian
Sage, Adam P.
Marshall, Erin A.
Stewart, Greg L.
Rock, Leigha D.
Garnis, Cathie
Lam, Wan L.
Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title_full Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title_fullStr Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title_full_unstemmed Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title_short Upgrading the Repertoire of miRNAs in Gastric Adenocarcinoma to Provide a New Resource for Biomarker Discovery
title_sort upgrading the repertoire of mirnas in gastric adenocarcinoma to provide a new resource for biomarker discovery
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6888638/
https://www.ncbi.nlm.nih.gov/pubmed/31739401
http://dx.doi.org/10.3390/ijms20225697
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