Evidence map›Paper›PMID 25639276›Full record

ArticleBiometrics2015

miRNA-target gene regulatory networks: A Bayesian integrative approach to biomarker selection with application to kidney cancer.

Thierry Chekouo, Francesco C Stingo, James D Doecke, Kim-Anh Do

Abstract readValidation Study
In one paragraph

Article in Biometrics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Bayesian graphical models for modern biological applications.Statistical methods & applications · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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.

Thierry ChekouoDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, 1400 Pressler Street, Unit 1411, Texas, 77030-3722, U.S.A.
Francesco C StingoDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, 1400 Pressler Street, Unit 1411, Texas, 77030-3722, U.S.A.
James D DoeckeCSIRO Computational Informatics/Australian e-Health Research Centre Level 5, UQ Health Sciences Building, 901/16 Royal Brisbane, Queensland, 4029, Australia.
Kim-Anh DoDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, 1400 Pressler Street, Unit 1411, Texas, 77030-3722, U.S.A.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The availability of cross-platform, large-scale genomic data has enabled the investigation of complex biological relationships for many cancers. Identification of reliable cancer-related biomarkers requires the characterization of multiple interactions across complex genetic networks. MicroRNAs are small non-coding RNAs that regulate gene expression; however, the direct relationship between a microRNA and its target gene is difficult to measure. We propose a novel Bayesian model to identify microRNAs and their target genes that are associated with survival time by incorporating the microRNA regulatory network through prior distributions. We assume that biomarkers involved in regulatory networks are likely associated with survival time. We employ non-local prior distributions and a stochastic search method for the selection of biomarkers associated with the survival outcome. We use KEGG pathway information to incorporate correlated gene effects within regulatory networks. Using simulation studies, we assess the performance of our method, and apply it to experimental data of kidney renal cell carcinoma (KIRC) obtained from The Cancer Genome Atlas. Our novel method validates previously identified cancer biomarkers and identifies biomarkers specific to KIRC progression that were not previously discovered. Using the KIRC data, we confirm that biomarkers involved in regulatory networks are more likely to be associated with survival time, showing connections in one regulatory network for five out of six such genes we identified.

Indexed as

Gene Regulatory NetworksAlgorithmsBayes TheoremBiomarkers, TumorBiometryCarcinoma, Renal CellComputer SimulationHumansKidney NeoplasmsMarkov ChainsMicroRNAsModels, GeneticModels, StatisticalMonte Carlo MethodRNA, NeoplasmBiomarkers, TumorMicroRNAsRNA, NeoplasmBayesian variable selectionGenomic dataMiRNA Regulatory networkNon-local prior

Identifiers

PMID25639276
PMCPMC4499566

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.