Cargando…

Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach

Aberrant microRNA (miRNA) expression is implicated in tumorigenesis. The underlying mechanisms are unclear because the regulations of each miRNA on potentially hundreds of mRNAs are sample specific. We describe a novel approach to infer Probabilistic MiRNA–mRNA Interaction Signature (‘ProMISe’) from...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Yue, Liang, Cheng, Wong, Ka-Chun, Jin, Ke, Zhang, Zhaolei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027195/
https://www.ncbi.nlm.nih.gov/pubmed/24609385
http://dx.doi.org/10.1093/nar/gku182
_version_ 1782316964205559808
author Li, Yue
Liang, Cheng
Wong, Ka-Chun
Jin, Ke
Zhang, Zhaolei
author_facet Li, Yue
Liang, Cheng
Wong, Ka-Chun
Jin, Ke
Zhang, Zhaolei
author_sort Li, Yue
collection PubMed
description Aberrant microRNA (miRNA) expression is implicated in tumorigenesis. The underlying mechanisms are unclear because the regulations of each miRNA on potentially hundreds of mRNAs are sample specific. We describe a novel approach to infer Probabilistic MiRNA–mRNA Interaction Signature (‘ProMISe’) from a single pair of miRNA–mRNA expression profile. Our model considers mRNA and miRNA competition as a probabilistic function of the expressed seeds (matches). To demonstrate ProMISe, we extensively exploited The Cancer Genome Atlas data. As a target predictor, ProMISe identifies more confidence/validated targets than other methods. Importantly, ProMISe confers higher cancer diagnostic power than using expression profiles alone. Gene set enrichment analysis on averaged ProMISe uniquely revealed respective target enrichments of oncomirs miR-21 and 145 in glioblastoma and ovarian cancers. Moreover, comparing matched breast (BRCA) and thyroid (THCA) tumor/normal samples uncovered thousands of tumor-related interactions. For example, ProMISe–BRCA network involves miR-155/183/21, which exhibits higher ProMISe coupled with coherently higher miRNA expression and lower target expression; oncomirs miR-221/222 in the ProMISe–THCA network engage with many downregulated target genes. Together, our probabilistic approach of integrating expression and sequence scores establishes a functional link between the aberrant miRNA and mRNA expression, which was previously under-appreciated due to the methodological differences.
format Online
Article
Text
id pubmed-4027195
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-40271952014-05-28 Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach Li, Yue Liang, Cheng Wong, Ka-Chun Jin, Ke Zhang, Zhaolei Nucleic Acids Res Methods Online Aberrant microRNA (miRNA) expression is implicated in tumorigenesis. The underlying mechanisms are unclear because the regulations of each miRNA on potentially hundreds of mRNAs are sample specific. We describe a novel approach to infer Probabilistic MiRNA–mRNA Interaction Signature (‘ProMISe’) from a single pair of miRNA–mRNA expression profile. Our model considers mRNA and miRNA competition as a probabilistic function of the expressed seeds (matches). To demonstrate ProMISe, we extensively exploited The Cancer Genome Atlas data. As a target predictor, ProMISe identifies more confidence/validated targets than other methods. Importantly, ProMISe confers higher cancer diagnostic power than using expression profiles alone. Gene set enrichment analysis on averaged ProMISe uniquely revealed respective target enrichments of oncomirs miR-21 and 145 in glioblastoma and ovarian cancers. Moreover, comparing matched breast (BRCA) and thyroid (THCA) tumor/normal samples uncovered thousands of tumor-related interactions. For example, ProMISe–BRCA network involves miR-155/183/21, which exhibits higher ProMISe coupled with coherently higher miRNA expression and lower target expression; oncomirs miR-221/222 in the ProMISe–THCA network engage with many downregulated target genes. Together, our probabilistic approach of integrating expression and sequence scores establishes a functional link between the aberrant miRNA and mRNA expression, which was previously under-appreciated due to the methodological differences. Oxford University Press 2014-05-01 2014-03-07 /pmc/articles/PMC4027195/ /pubmed/24609385 http://dx.doi.org/10.1093/nar/gku182 Text en © The Author(s) 2014. Published by Oxford University Press [on behalf of Nucleic Acids Research]. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Li, Yue
Liang, Cheng
Wong, Ka-Chun
Jin, Ke
Zhang, Zhaolei
Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title_full Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title_fullStr Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title_full_unstemmed Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title_short Inferring probabilistic miRNA–mRNA interaction signatures in cancers: a role-switch approach
title_sort inferring probabilistic mirna–mrna interaction signatures in cancers: a role-switch approach
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027195/
https://www.ncbi.nlm.nih.gov/pubmed/24609385
http://dx.doi.org/10.1093/nar/gku182
work_keys_str_mv AT liyue inferringprobabilisticmirnamrnainteractionsignaturesincancersaroleswitchapproach
AT liangcheng inferringprobabilisticmirnamrnainteractionsignaturesincancersaroleswitchapproach
AT wongkachun inferringprobabilisticmirnamrnainteractionsignaturesincancersaroleswitchapproach
AT jinke inferringprobabilisticmirnamrnainteractionsignaturesincancersaroleswitchapproach
AT zhangzhaolei inferringprobabilisticmirnamrnainteractionsignaturesincancersaroleswitchapproach