Evidence map›Paper›PMID 22227207›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2012

miR-21 regulates chronic hypoxia-induced pulmonary vascular remodeling.

Shanzhong Yang, Sami Banerjee, Andressa de Freitas, Huachun Cui, Na Xie, Edward Abraham, Gang Liu

Abstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 177 citations in OpenAlex.

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  15. Effects of microRNA-21 on endothelial-to-mesenchymal transition and its role in the pathogenesis of chronic obstructive pulmonary disease.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Hydrogen sulfide and miR21 are suitable biomarkers of hypoxic exposure.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  20. Review

44 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

7 authors at 1 institution in 1 country.

Shanzhong YangDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Alabama, Birmingham, USA.
Sami Banerjee
Andressa de Freitas
Huachun Cui
Na Xie
Edward Abraham
Gang Liu
University of Alabama at Birmingham · US

Funding

Urokinase, Neutrophil Activation and Acute Lung Injury.R01HL076206 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI LIU, GANG · 2005 to 2013
$2.8M
miR-21 and lung fibrosisR01HL105473 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, GANG · 2011 to 2015
$1.8M
MicroRNAs, inflammation, and acute lung injury.R21HL097218 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, GANG · 2010 to 2011
$403k
NHLBI NIH HHS HL-076206NHLBI NIH HHS HL-097218NHLBI NIH HHS HL-105473NHLBI NIH HHS R01 HL105473
6 · The paper itself

Abstract

Chronic hypoxia causes pulmonary vascular remodeling leading to pulmonary hypertension (PH) and right ventricle (RV) hypertrophy. Aberrant expression of microRNA (miRNA) is closely associated with a number of pathophysiologic processes. However, the role of miRNAs in chronic hypoxia-induced pulmonary vascular remodeling and PH has not been well characterized. In this study, we found increased expression of miR-21 in distal small arteries in the lungs of hypoxia-exposed mice. Putative miR-21 targets, including bone morphogenetic protein receptor (BMPR2), WWP1, SATB1, and YOD1, were downregulated in the lungs of hypoxia-exposed mice and in human pulmonary artery smooth muscle cells (PASMCs) overexpressing miR-21. We found that sequestration of miR-21, either before or after hypoxia exposure, diminished chronic hypoxia-induced PH and attenuated hypoxia-induced pulmonary vascular remodeling, likely through relieving the suppressed expression of miR-21 targets in the lungs of hypoxia-exposed mice. Overexpression of miR-21 enhanced, whereas downregulation of miR-21 diminished, the proliferation of human PASMCs in vitro and the expression of cell proliferation associated proteins, such as proliferating cell nuclear antigen, cyclin D1, and Bcl-xL. Our data suggest that miR-21 plays an important role in the pathogenesis of chronic hypoxia-induced pulmonary vascular remodeling and also suggest that miR-21 is a potential target for novel therapeutics to treat chronic hypoxia associated pulmonary diseases.

Indexed as

Airway RemodelingAnimalsApoptosisbcl-X ProteinBone Morphogenetic Protein Receptors, Type IICell Cycle ProteinsCell LineCell ProliferationCyclin D1Down-RegulationHumansHypertension, PulmonaryHypertrophy, Right VentricularHypoxiaLungMatrix Attachment Region Binding ProteinsBCL2L1 protein, humanbcl-X ProteinBmpr2 protein, mouseBone Morphogenetic Protein Receptors, Type IICCND1 protein, humanCell Cycle ProteinsCyclin D1Matrix Attachment Region Binding ProteinsMicroRNAsMIRN21 microRNA, mouseSatb1 protein, mouseUbiquitin-Protein LigasesWWP1 protein, mouse

Identifiers

PMID22227207
PMCPMC3311531
OpenAlexW2076256652

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.