Evidence map›Paper›PMID 22911455›Full record

ArticlePhysiological genomics2012

Identification of microRNAs changed in the neonatal lungs in response to hyperoxia exposure.

Manoj Bhaskaran, Dong Xi, Yang Wang, Chaoqun Huang, Telugu Narasaraju, Weiqun Shu, Chunling Zhao, Xiao Xiao, Sunil More, Melanie Breshears and 1 more

Abstract read
In one paragraph

Article in Physiological genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  5. [Expression and regulatory mechanism of miR-34a in neonatal rat model of bron-chopulmonary dysplasia induced by hyperoxia].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
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  15. Glycoprotein nonmetastatic melanoma protein B: A key mediator and an emerging therapeutic target in autoimmune diseases.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 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

11 authors at 2 institutions in 2 countries.

Manoj BhaskaranThe Lundberg-Kienlen Lung Biology and Toxicology Laboratory, Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, OK 74078, USA.
Dong Xi
Yang Wang
Chaoqun Huang
Telugu Narasaraju
Weiqun Shu
Chunling Zhao
Xiao Xiao
Sunil More
Melanie Breshears
Lin Liu
Oklahoma State University · USArmy Medical University · CN

Funding

Mechanisms of Alveolar Fluid TransportR01HL083188 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2006 to 2009
$1.4M
Role of MicroRNAs in Bronchopulmonary DysplasiaR21HL087884 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2009 to 2010
$406k
MicroRNA Expression Profiling in Idiopathic Pulmonary FibrosisR03HL095383 · NHLBI · OKLAHOMA STATE UNIVERSITY STILLWATER · PI LIU, LIN · 2009 to 2010
$148k
NHLBI NIH HHS HL-083188NHLBI NIH HHS HL-087884NHLBI NIH HHS HL-095383NHLBI NIH HHS R01 HL083188NHLBI NIH HHS R03 HL095383NHLBI NIH HHS R21 HL087884
6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a multifactorial chronic lung disease of premature infants. BPD can be attributed to the dysregulation of normal lung development due to ventilation and oxygen toxicity, resulting in pathologic complications of impaired alveolarization and vascularization. MicroRNAs (miRNA) are small noncoding RNAs that regulate gene expression posttranscriptionally and are implicated in diverse biological processes and diseases. The objectives of this study are to identify the changed miRNAs and their target genes in neonatal rat lungs in response to hyperoxia exposure. Using miRNA microarray and real-time PCR analyses, we found downregulation of five miRNAs, miR-342, miR-335, miR-150, miR-126*, and miR-151*, and upregulation of two miRNAs, miR-21 and miR-34a. Some of these miRNAs had the highest expression during embryonic and early postnatal development. DNA microarray analysis yielded several genes with conserved binding sites for these altered miRNAs. Glycoprotein nonmetastatic melanoma protein b (GPNMB) was experimentally verified as a target of miR-150. In summary, we identified seven miRNAs that were changed in hyperoxia-exposed neonatal lungs. These results provide a basis for deciphering the mechanisms involved in the spatial and temporal regulation of proteins that contribute to the pathogenesis of BPD.

Indexed as

3' Untranslated RegionsAnimalsAnimals, NewbornBinding SitesBronchopulmonary DysplasiaCell LineDisease Models, AnimalGenes, ReporterHumansHyperoxiaInfant, NewbornLungMembrane GlycoproteinsMicroRNAsModels, BiologicalOligonucleotide Array Sequence Analysis3' Untranslated RegionsGpnmb protein, ratMembrane GlycoproteinsMicroRNAs

Identifiers

PMID22911455
PMCPMC3472467
OpenAlexW2132349221

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.