Evidence map›Paper›PMID 25378249›Full record

ArticleGenome research2015

Cupid: simultaneous reconstruction of microRNA-target and ceRNA networks.

Hua-Sheng Chiu, David Llobet-Navas, Xuerui Yang, Wei-Jen Chung, Alberto Ambesi-Impiombato, Archana Iyer, Hyunjae Ryan Kim, Elena G Seviour, Zijun Luo, Vasudha Sehgal and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing 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

63 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Modeling ncRNA Synergistic Regulation in Cancer.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Competing endogenous RNAs (ceRNAs) and drug resistance to cancer therapy.Cancer drug resistance (Alhambra, Calif.) · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Computational Detection of MicroRNA Targets.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  14. Article
  15. Bioinformatics Methods for Modeling microRNA Regulatory Networks in Cancer.Advances in experimental medicine and biology · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

3 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

17 authors at 7 institutions in 2 countries.

Hua-Sheng ChiuDepartment of Systems Biology, Center for Computational Biology and Bioinformatics, Department of Biomedical Informatics, Columbia University, New York, New York 10032, USA; Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA;
David Llobet-NavasDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA;
Xuerui YangMOE Key Laboratory of Bioinformatics, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China;
Wei-Jen ChungDepartment of Systems Biology, Center for Computational Biology and Bioinformatics, Department of Biomedical Informatics, Columbia University, New York, New York 10032, USA;
Alberto Ambesi-ImpiombatoInstitute for Cancer Genetics, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York 10032, USA;
Archana IyerDepartment of Systems Biology.
Hyunjae Ryan KimLaboratory of RNA Molecular Biology, Rockefeller University, New York, New York 10065, USA;
Elena G SeviourDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
Zijun LuoDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
Vasudha SehgalDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
Tyler MossDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
Yiling LuDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA; califano@c2b2.columbia.edu sumazin@bcm.edu.
Prahlad RamDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
José SilvaDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA;
Gordon B MillsDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA;
Andrea CalifanoDepartment of Systems Biology, Center for Computational Biology and Bioinformatics, Department of Biomedical Informatics, Columbia University, New York, New York 10032, USA; Institute for Cancer Genetics, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, New York 10032, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York 10032, USA califano@c2b2.columbia.edu sumazin@bcm.edu.
Pavel SumazinTexas Children's Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA;
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USCenter for Systems Biology · USColumbia University Irving Medical Center · USIcahn School of Medicine at Mount Sinai · USKing Center · USRockefeller University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
Systems-Based Predictions of Responses to Cancer TherapyU54CA112970 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI MILLS, GORDON B. · 2004 to 2014
$27.1M
Profiling Signatures of synergistic Chemical Perturbations in Diverse Cellular CU01CA164184 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2011 to 2013
$2.1M
Genetic Network Inference with Combinational PhenotypesR01CA109755 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2009
$1.9M
A Systems Approach to Elucidate Mechanisms od Drug Activity and SensivityU01HL111566 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2011 to 2013
$1.1M
NCI NIH HHS 5U01CA164184-02NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA109755NCI NIH HHS R01CA109755NCI NIH HHS U01 CA164184NCI NIH HHS U54 CA112970NCI NIH HHS U54 CA121852NCI NIH HHS U54CA121852NHLBI NIH HHS 1U01HL111566-01NHLBI NIH HHS U01 HL111566
6 · The paper itself

Abstract

We introduce a method for simultaneous prediction of microRNA-target interactions and their mediated competitive endogenous RNA (ceRNA) interactions. Using high-throughput validation assays in breast cancer cell lines, we show that our integrative approach significantly improves on microRNA-target prediction accuracy as assessed by both mRNA and protein level measurements. Our biochemical assays support nearly 500 microRNA-target interactions with evidence for regulation in breast cancer tumors. Moreover, these assays constitute the most extensive validation platform for computationally inferred networks of microRNA-target interactions in breast cancer tumors, providing a useful benchmark to ascertain future improvements.

Indexed as

Epistasis, GeneticGene Regulatory NetworksRNA Interference3' Untranslated RegionsAlgorithmsBinding SitesBreast NeoplasmsCell Line, TumorCluster AnalysisComputational BiologyEstrogen Receptor alphaFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMicroRNAs3' Untranslated RegionsESR1 protein, humanEstrogen Receptor alphaMicroRNAsRNA, Messenger

Identifiers

PMID25378249
PMCPMC4315299
OpenAlexW2096381177

What OpenQuestion holds

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LicenceCC BY-NC
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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.