Evidence map›Paper›PMID 24906430›Full record

ArticleBreast cancer research and treatment2014

HITS-CLIP reveals key regulators of nuclear receptor signaling in breast cancer.

Manoj M Pillai, Austin E Gillen, Tomomi M Yamamoto, Enos Kline, Joseph Brown, Kale Flory, Jay R Hesselberth, Peter Kabos

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  4. Review
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  7. Article
  8. Article
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  11. Upregulated miRNAs on theFrontiers in genetics · 2022
    Article
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  14. Review
  15. Article
  16. Article
  17. Genes · 2020
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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

8 authors at 2 institutions in 1 country.

Manoj M PillaiSection of Hematology, Yale Cancer Center, New Haven, CT, USA.
Austin E Gillen
Tomomi M Yamamoto
Enos Kline
Joseph Brown
Kale Flory
Jay R Hesselberth
Peter Kabos
University of Colorado Denver · USYale Cancer Center · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Role of microRNAs in regulation of the marrow microenvironmentR01HL104070 · NHLBI · YALE UNIVERSITY · PI PILLAI, MANOJ M. · 2011 to 2015
$2.2M
Regulation of anti-endocrine resistance of breast cancer by a network of non-codiK08CA164048 · NCI · UNIVERSITY OF COLORADO DENVER · PI KABOS, PETER · 2012 to 2016
$859k
Monocyte derived CXCL7 in the marrow microenvironmentK08DK073701 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI PILLAI, MANOJ M. · 2006 to 2010
$641k
NCATS NIH HHS UL1 TR001082NCI NIH HHS CA164048NCI NIH HHS K08 CA164048NCI NIH HHS P30 CA046934NHLBI NIH HHS HL104070NHLBI NIH HHS R01 HL104070NIDDK NIH HHS DK073701NIDDK NIH HHS K08 DK073701
6 · The paper itself

Abstract

miRNAs regulate the expression of genes in both normal physiology and disease. While miRNAs have been demonstrated to play a pivotal role in aspects of cancer biology, these reports have generally focused on the regulation of single genes. Such single-gene approaches have significant limitations, relying on miRNA expression levels and heuristic predictions of mRNA-binding sites. This results in only circumstantial evidence of miRNA-target interaction and typically leads to large numbers of false positive predictions. Here, we used a genome-wide approach (high-throughput sequencing of RNA isolated by crosslinking immunoprecipitation, HITS-CLIP) to define direct miRNA-mRNA interactions in three breast cancer subtypes (estrogen receptor positive, Her2 amplified, and triple negative). Focusing on steroid receptor signaling, we identified two novel regulators of the ER pathway (miR-9-5p and miR-193a/b-3p), which together target multiple genes involved in ER signaling. Moreover, this approach enabled the definition of miR-9-5p as a global regulator of steroid receptor signaling in breast cancer. We show that miRNA targets and networks defined by HITS-CLIP under physiologic conditions are predictive of patient outcomes and provide global insight into miRNA regulation in breast cancer.

Indexed as

Signal TransductionBreast NeoplasmsCell Line, TumorCluster AnalysisEstrogensFemaleGene Expression ProfilingGene Regulatory NetworksHigh-Throughput Nucleotide SequencingHumansImmunoprecipitationMicroRNAsNeoplasm GradingPrognosisReceptors, Cytoplasmic and NuclearReceptors, EstrogenEstrogensMicroRNAsMIRN92 microRNA, humanReceptors, Cytoplasmic and NuclearReceptors, EstrogenReceptors, SteroidRNA, Messenger

Identifiers

PMID24906430
PMCPMC4115274
OpenAlexW2022725285

What OpenQuestion holds

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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.