Evidence map›Paper›PMID 22454450›Full record

ArticlePhysiological genomics2012

Dynamic microRNA expression during the transition from right ventricular hypertrophy to failure.

Sushma Reddy, Mingming Zhao, Dong-Qing Hu, Giovanni Fajardo, Shijun Hu, Zhumur Ghosh, Viswanathan Rajagopalan, Joseph C Wu, Daniel Bernstein

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 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Epigenetic Mechanisms in Heart Diseases.Reviews in cardiovascular medicine · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Posttranscriptional Regulation by Proteins and Noncoding RNAs.Advances in experimental medicine and biology · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

10 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

9 authors at 1 institution in 1 country.

Sushma ReddyDepartment of Pediatrics, Stanford University School of Medicine, Stanford, California 94305, USA. sureddy@stanford.edu
Mingming Zhao
Dong-Qing Hu
Giovanni Fajardo
Shijun Hu
Zhumur Ghosh
Viswanathan Rajagopalan
Joseph C Wu
Daniel Bernstein
Stanford University · US

Funding

ROLE OF BETA-RECEPTOR SIGNALING IN CARDIOMYOPATHYR01HL061535 · NHLBI · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL · 2000 to 2010
$3.3M
09: Inducing Pluripotency with MiRNAs: New Paradigm Shif in Cell ReprogrammingDP2OD004437 · OD · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2008 to 2008
$2.4M
Integrated Strategies for Novel Treatment of Myocardial IschemiaR01HL095571 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2010 to 2014
$2.0M
NHLBI NIH HHS HL-061535NHLBI NIH HHS R01 HL095571NHLBI NIH HHS R01HL-095571NIH HHS DP2 OD004437NIH HHS DP2OD004437
6 · The paper itself

Abstract

MicroRNAs (miRs) are small, noncoding RNAs that are emerging as crucial regulators of cardiac remodeling in left ventricular hypertrophy (LVH) and failure (LVF). However, there are no data on their role in right ventricular hypertrophy (RVH) and failure (RVF). This is a critical question given that the RV is uniquely at risk in patients with congenital right-sided obstructive lesions and in those with systemic RVs. We have developed a murine model of RVH and RVF using pulmonary artery constriction (PAC). miR microarray analysis of RV from PAC vs. control demonstrates altered miR expression with gene targets associated with cardiomyocyte survival and growth during hypertrophy (miR 199a-3p) and reactivation of the fetal gene program during heart failure (miR-208b). The transition from hypertrophy to heart failure is characterized by apoptosis and fibrosis (miRs-34, 21, 1). Most are similar to LVH/LVF. However, there are several key differences between RV and LV: four miRs (34a, 28, 148a, and 93) were upregulated in RVH/RVF that are downregulated or unchanged in LVH/LVF. Furthermore, there is a corresponding downregulation of their putative target genes involving cell survival, proliferation, metabolism, extracellular matrix turnover, and impaired proteosomal function. The current study demonstrates, for the first time, alterations in miRs during the process of RV remodeling and the gene regulatory pathways leading to RVH and RVF. Many of these alterations are similar to those in the afterload-stressed LV. miRs differentially regulated between the RV and LV may contribute to the RVs increased susceptibility to heart failure.

Indexed as

Gene Expression ProfilingAnimalsBlotting, WesternCalcium-Calmodulin-Dependent Protein Kinase Type 2Cluster AnalysisDisease Models, AnimalDisease ProgressionHeart FailureHumansHypertrophy, Right VentricularMaleMiceMicroRNAsOligonucleotide Array Sequence AnalysisProto-Oncogene Proteins c-aktReverse Transcriptase Polymerase Chain ReactionCalcium-Calmodulin-Dependent Protein Kinase Type 2MicroRNAsMirn148 microRNA, mouseMirn93 microRNA, mouseProto-Oncogene Proteins c-akt

Identifiers

PMID22454450
PMCPMC3426410
OpenAlexW1980402405

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.