Evidence map›Paper›PMID 24609385›Full record

ArticleNucleic acids research2014

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

Yue Li, Cheng Liang, Ka-Chun Wong, Ke Jin, Zhaolei Zhang

Abstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Article
  2. Temporal Expression Analysis to Unravel Gene Regulatory Dynamics by microRNAs.Methods in molecular biology (Clifton, N.J.) · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yue LiDepartment of Computer Science, University of Toronto, Toronto, Ontario M5S 3G4, Canada The Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada.
Cheng LiangThe Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada.
Ka-Chun WongDepartment of Computer Science, University of Toronto, Toronto, Ontario M5S 3G4, Canada The Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada.
Ke JinThe Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A4, Canada.
Zhaolei ZhangDepartment of Computer Science, University of Toronto, Toronto, Ontario M5S 3G4, Canada The Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A4, Canada Banting and Best Department of Medical Research, University of Toronto, Toronto, ON M5S 3E1, Canada zhaolei.zhang@utoronto.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Models, GeneticAlgorithmsBiomarkers, TumorBreast NeoplasmsCell Line, TumorFemaleGene ExpressionGene Expression Regulation, NeoplasticGene Regulatory NetworksHEK293 CellsHumansMicroRNAsModels, StatisticalOncogenesRNA InterferenceRNA, MessengerBiomarkers, TumorMicroRNAsRNA, Messenger

Identifiers

PMID24609385
PMCPMC4027195

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.