Evidence map›Paper›PMID 26169799›Full record

ArticleGenomics, proteomics & bioinformatics2015

Correlating bladder cancer risk genes with their targeting microRNAs using MMiRNA-Tar.

Yang Liu, Steve Baker, Hui Jiang, Gary Stuart, Yongsheng Bai

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. MMiRNA-ViewerBMC bioinformatics · 2020
    Article
  2. Article
  3. Article
  4. Sputum Exosomal microRNAs Profiling Reveals Critical Pathways Modulated ByInternational journal of chronic obstructive pulmonary disease · 2019
    Article
  5. Article
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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 at 3 institutions in 1 country.

Yang LiuDepartment of Electrical and Computer Engineering, Rose-Hulman Institute of Technology, Terre Haute, IN 47803, USA.
Steve BakerDepartment of Math and Computer Science, Indiana State University, Terre Haute, IN 47809, USA.
Hui JiangDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.
Gary StuartDepartment of Biology, Indiana State University, Terre Haute, IN 47809, USA; The Center for Genomic Advocacy, Indiana State University, Terre Haute, IN 47809, USA.
Yongsheng BaiDepartment of Biology, Indiana State University, Terre Haute, IN 47809, USA; The Center for Genomic Advocacy, Indiana State University, Terre Haute, IN 47809, USA. Electronic address: Yongsheng.Bai@indstate.edu.
Indiana State University · USRose–Hulman Institute of Technology · USUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Cancer Genome Atlas (TCGA) (http://cancergenome.nih.gov) is a valuable data resource focused on an increasing number of well-characterized cancer genomes. In part, TCGA provides detailed information about cancer-dependent gene expression changes, including changes in the expression of transcription-regulating microRNAs. We developed a web interface tool MMiRNA-Tar (http://bioinf1.indstate.edu/MMiRNA-Tar) that can calculate and plot the correlation of expression for mRNA-microRNA pairs across samples or over a time course for a list of pairs under different prediction confidence cutoff criteria. Prediction confidence was established by requiring that the proposed mRNA-microRNA pair appears in at least one of three target prediction databases: TargetProfiler, TargetScan, or miRanda. We have tested our MMiRNA-Tar tool through analyzing 53 tumor and 11 normal samples of bladder urothelial carcinoma (BLCA) datasets obtained from TCGA and identified 204 microRNAs. These microRNAs were correlated with the mRNAs of five previously-reported bladder cancer risk genes and these selected pairs exhibited correlations in opposite direction between the tumor and normal samples based on the customized cutoff criterion of prediction. Furthermore, we have identified additional 496 genes (830 pairs) potentially targeted by 79 significant microRNAs out of 204 using three cutoff criteria, i.e., false discovery rate (FDR)<0.1, opposite correlation coefficient between the tumor and normal samples, and predicted by at least one of three target prediction databases. Therefore, MMiRNA-Tar provides researchers a convenient tool to visualize the co-relationship between microRNAs and mRNAs and to predict their targeting relationship. We believe that correlating expression profiles for microRNAs and mRNAs offers a complementary approach for elucidating their interactions.

Indexed as

Databases, GeneticBiomarkers, TumorGene Expression ProfilingGenetic MarkersGenomeHumansMicroRNAsRNA, MessengerUrinary Bladder NeoplasmsBiomarkers, TumorGenetic MarkersMicroRNAsRNA, MessengerBladder cancerCorrelationMicroRNAmRNATarget predictionThe Cancer Genome Atlas

Identifiers

PMID26169799
PMCPMC4563352
OpenAlexW902285478

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.