Evidence map›Paper›PMID 31425002›Full record

ArticleRNA biology2019

Transcriptomic studies provide insights into the tumor suppressive role of miR-146a-5p in non-small cell lung cancer (NSCLC) cells.

Joseph R Iacona, Nicholas J Monteleone, Alexander D Lemenze, Ashley L Cornett, Carol S Lutz

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Review
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  7. Cell Behavior of Non-Small Cell Lung Cancer Is at EGFR and MicroRNAs Hands.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Review
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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 1 institution in 2 countries.

Joseph R IaconaDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.ORCID 0000-0001-6382-0207
Nicholas J MonteleoneDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.ORCID 0000-0001-6576-0324
Alexander D LemenzeNewark Health Sciences Campus, Rutgers University School of Graduate Studies, Newark, NJ, USA.ORCID 0000-0003-3053-0849
Ashley L CornettDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.
Carol S LutzDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.ORCID 0000-0002-7283-072X
Rutgers, The State University of New Jersey · US

Funding

COX-2 Functions in Bone Fracture HealingR01AR069044 · NIAMS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI O'CONNOR, J PATRICK · 2016 to 2020
$2.1M
NIAMS NIH HHS R01 AR069044
6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is a complex disease in need of new methods of therapeutic intervention. Recent interest has focused on using microRNAs (miRNAs) as a novel treatment method for various cancers. miRNAs negatively regulate gene expression post-transcriptionally, and have become attractive candidates for cancer treatment because they often simultaneously target multiple genes of similar biological function. One such miRNA is miR-146a-5p, which has been described as a tumor suppressive miRNA in NSCLC cell lines and tissues. In this study, we performed RNA-Sequencing (RNA-Seq) analysis following transfection of synthetic miR-146a-5p in an NSCLC cell line, A549, and validated our data with Gene Ontology and qRT-PCR analysis of known miR-146a-5p target genes. Our transcriptomic data revealed that miR-146a-5p exerts its tumor suppressive function beyond previously reported targeting of EGFR and NF-κB signaling. miR-146a-5p mimic transfection downregulated arachidonic acid metabolism genes, the RNA-binding protein HuR, and many HuR-stabilized pro-cancer mRNAs, including TGF-β, HIF-1α, and various cyclins. miR-146a-5p transfection also reduced expression and cellular release of the chemokine CCL2, and this effect was mediated through the 3' untranslated region of its mRNA. Taken together, our work reveals that miR-146a-5p functions as a tumor suppressor in NSCLC by controlling various metabolic and signaling pathways through direct and indirect mechanisms.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptomeA549 CellsAdenocarcinoma of LungAnimalsArachidonic AcidAtlases as TopicCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellChemokine CCL2CyclinsELAV-Like Protein 1Gene Expression ProfilingHumansHypoxia-Inducible Factor 1, alpha SubunitLung NeoplasmsArachidonic AcidCCL2 protein, humanChemokine CCL2CyclinsELAVL1 protein, humanELAV-Like Protein 1HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN146 microRNA, humanTGFB1 protein, humanTransforming Growth Factor beta1CCL2gene expressionHuRInflammationlung adenocarcinomamicroRNApost-transcriptional regulationRNA-Seq

Identifiers

PMID31425002
PMCPMC6844565
OpenAlexW2969453015

What OpenQuestion holds

Textmetadata
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.