Evidence map›Paper›PMID 26817421›Full record

ArticleBMC genomics2016

Identification of miRNA-mRNA regulatory modules by exploring collective group relationships.

S M Masud Karim, Lin Liu, Thuc Duy Le, Jiuyong Li

Abstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. A review on methods for predicting miRNA-mRNA regulatory modules.Journal of integrative bioinformatics · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. MicroRNA heterogeneity in melanoma progression.Seminars in cancer biology · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Review
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

4 authors.

S M Masud KarimSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Adelaide, 5095, SA, Australia. masud.karim@mymail.unisa.edu.au.
Lin LiuSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Adelaide, 5095, SA, Australia. Lin.Liu@unisa.edu.au.
Thuc Duy LeSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Adelaide, 5095, SA, Australia. Thuc.Le@unisa.edu.au.
Jiuyong LiSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Adelaide, 5095, SA, Australia. Jiuyong.Li@unisa.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundmicroRNAs (miRNAs) play an essential role in the post-transcriptional gene regulation in plants and animals. They regulate a wide range of biological processes by targeting messenger RNAs (mRNAs). Evidence suggests that miRNAs and mRNAs interact collectively in gene regulatory networks. The collective relationships between groups of miRNAs and groups of mRNAs may be more readily interpreted than those between individual miRNAs and mRNAs, and thus are useful for gaining insight into gene regulation and cell functions. Several computational approaches have been developed to discover miRNA-mRNA regulatory modules (MMRMs) with a common aim to elucidate miRNA-mRNA regulatory relationships. However, most existing methods do not consider the collective relationships between a group of miRNAs and the group of targeted mRNAs in the process of discovering MMRMs. Our aim is to develop a framework to discover MMRMs and reveal miRNA-mRNA regulatory relationships from the heterogeneous expression data based on the collective relationships.

resultsWe propose DIscovering COllective group RElationships (DICORE), an effective computational framework for revealing miRNA-mRNA regulatory relationships. We utilize the notation of collective group relationships to build the computational framework. The method computes the collaboration scores of the miRNAs and mRNAs on the basis of their interactions with mRNAs and miRNAs, respectively. Then it determines the groups of miRNAs and groups of mRNAs separately based on their respective collaboration scores. Next, it calculates the strength of the collective relationship between each pair of miRNA group and mRNA group using canonical correlation analysis, and the group pairs with significant canonical correlations are considered as the MMRMs. We applied this method to three gene expression datasets, and validated the computational discoveries.

conclusionsAnalysis of the results demonstrates that a large portion of the regulatory relationships discovered by DICORE is consistent with the experimentally confirmed databases. Furthermore, it is observed that the top mRNAs that are regulated by the miRNAs in the identified MMRMs are highly relevant to the biological conditions of the given datasets. It is also shown that the MMRMs identified by DICORE are more biologically significant and functionally enriched.

Indexed as

Computational BiologyAlgorithmsAnimalsDatabases, GeneticGene Regulatory NetworksHumansMicroRNAsNeoplasmsRNA, MessengerTranscriptomeMicroRNAsRNA, Messenger

Identifiers

PMID26817421
PMCPMC4895272

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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.