Evidence map›Paper›PMID 22745231›Full record

ArticleGenome research2012

A miRNA-regulatory network explains how dysregulated miRNAs perturb oncogenic processes across diverse cancers.

Christopher L Plaisier, Min Pan, Nitin S Baliga

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing 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

111 citing papers in PubMed, 201 citations in OpenAlex.

  1. Review
  2. Article
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  7. Review
  8. Article
  9. A gene set enrichment analysis for cancer hallmarks.Journal of pharmaceutical analysis · 2025
    Article
  10. Article
  11. Article
  12. REMR: Identification of RNA Editing-mediated MiRNA Regulation in Cancers.Computational and structural biotechnology journal · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Animal cells and systems · 2024
    Article
  18. Article
  19. Article
  20. Regulation of ERα-dependent breast cancer metastasis by a miR-29a signaling.Journal of experimental & clinical cancer research : CR · 2023
    Article

51 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Christopher L PlaisierInstitute for Systems Biology, Seattle, WA 98109-5234, USA.
Min Pan
Nitin S Baliga
Institute for Systems Biology · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
Interrogation of systems level mechanisms controlling DNA repair processesR01GM077398 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2007 to 2010
$1.3M
NIGMS NIH HHS 1R01GM077398-01A2NIGMS NIH HHS P50 GM076547NIGMS NIH HHS P50GM076547NIGMS NIH HHS R01 GM077398
6 · The paper itself

Abstract

Genes regulated by the same miRNA can be discovered by virtue of their coexpression at the transcriptional level and the presence of a conserved miRNA-binding site in their 3' UTRs. Using this principle we have integrated the three best performing and complementary algorithms into a framework for inference of regulation by miRNAs (FIRM) from sets of coexpressed genes. We demonstrate the utility of FIRM by inferring a cancer-miRNA regulatory network through the analysis of 2240 gene coexpression signatures from 46 cancers. By analyzing this network for functional enrichment of known hallmarks of cancer we have discovered a subset of 13 miRNAs that regulate oncogenic processes across diverse cancers. We have performed experiments to test predictions from this miRNA-regulatory network to demonstrate that miRNAs of the miR-29 family (miR-29a, miR-29b, and miR-29c) regulate specific genes associated with tissue invasion and metastasis in lung adenocarcinoma. Further, we highlight the specificity of using FIRM inferences to identify miRNA-regulated genes by experimentally validating that miR-767-5p, which partially shares the miR-29 seed sequence, regulates only a subset of miR-29 targets. By providing mechanistic linkage between miRNA dysregulation in cancer, their binding sites in the 3'UTRs of specific sets of coexpressed genes, and their associations with known hallmarks of cancer, FIRM, and the inferred cancer miRNA-regulatory network will serve as a powerful public resource for discovery of potential cancer biomarkers.

Indexed as

Gene Expression Regulation, NeoplasticGene Regulatory Networks3' Untranslated RegionsAdenocarcinomaAlgorithmsBinding SitesDNA, NeoplasmHumansLung NeoplasmsMicroRNAsNeoplasm MetastasisSequence Analysis, RNATranscriptome3' Untranslated RegionsDNA, NeoplasmMicroRNAsMIRN29a microRNA, human

Identifiers

PMID22745231
PMCPMC3483559
OpenAlexW2112012611

What OpenQuestion holds

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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.