Evidence map›Paper›PMID 19147652›Full record

ArticleCardiovascular research2009

MicroRNA expression in response to murine myocardial infarction: miR-21 regulates fibroblast metalloprotease-2 via phosphatase and tensin homologue.

Sashwati Roy, Savita Khanna, Syed-Rehan A Hussain, Sabyasachi Biswas, Ali Azad, Cameron Rink, Surya Gnyawali, Shani Shilo, Gerard J Nuovo, Chandan K Sen

Open access · bronzeAbstract read
In one paragraph

Article in Cardiovascular research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 297 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
297citing papers in PubMed, 2 pooled it
19.6field-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

297 citing papers in PubMed, 2 syntheses or guidelines pooled it, 611 citations in OpenAlex.

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  7. Mapping GlycoRNAs on an Exosomal Surface.Journal of the American Chemical Society · 2026
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237 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Sashwati RoyDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University Medical Center, 473 West 12th Avenue, Columbus, OH 43210, USA.
Savita Khanna
Syed-Rehan A Hussain
Sabyasachi Biswas
Ali Azad
Cameron Rink
Surya Gnyawali
Shani Shilo
Gerard J Nuovo
Chandan K Sen
The Ohio State University Wexner Medical Center · USThe Ohio State University · US

Funding

Redox Control of Wound HealingR01GM069589 · NIGMS · OHIO STATE UNIVERSITY · PI SEN, CHANDAN K · 2004 to 2013
$2.3M
Oxygen Sensitive Signaling in Primary Cardiac FibroblastR01HL073087 · NHLBI · OHIO STATE UNIVERSITY · PI SEN, CHANDAN K · 2004 to 2007
$1.3M
Mechanisms underlying impaired diabetic wound healingR01DK076566 · NIDDK · OHIO STATE UNIVERSITY · PI ROY, SASHWATI · 2008 to 2011
$1.2M
NHLBI NIH HHS R01-HL073087NIDDK NIH HHS R01 DK076566NIGMS NIH HHS R01 GM069589
6 · The paper itself

Abstract

aimsMicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level by either degradation or translational repression of a target mRNA. Encoded in the genome of most eukaryotes, miRNAs have been proposed to regulate specifically up to 90% of human genes through a process known as miRNA-guided RNA silencing. For the first time, we sought to test how myocardial ischaemia-reperfusion (IR) changes miR expression. METHODS AND

resultsFollowing 2 and 7 h of IR or sham operation, myocardial tissue was collected and subjected to miRNA expression profiling and quantification using a Bioarray system that screens for human-, mice-, rat-, and Ambi-miR. Data mining and differential analyses resulted in 13 miRs that were up-regulated on day 2, 9 miRs that were up-regulated on day 7, and 6 miRs that were down-regulated on day 7 post-IR. Results randomly selected from expression profiling were validated using real-time PCR. Tissue elements laser-captured from the infarct site showed marked induction of miR-21. In situ hybridization studies using locked nucleic acid miR-21-specific probe identified that IR-inducible miR-21 was specifically localized in the infarct region of the IR heart. Immunohistochemistry data show that cardiac fibroblasts (CFs) are the major cell type in the infarct zone. Studies with isolated CFs demonstrated that phosphatase and tensin homologue (PTEN) is a direct target of miR-21. Modulation of miR-21 regulated expression of matrix metalloprotease-2 (MMP-2) via a PTEN pathway. Finally, we noted a marked decrease in PTEN expression in the infarct zone. This decrease was associated with increased MMP-2 expression in the infarct area.

conclusionThis work constitutes the first report describing changes in miR expression in response to IR in the mouse heart, showing that miR-21 regulates MMP-2 expression in CFs of the infarct zone via a PTEN pathway.

Indexed as

Gene Expression Regulation, EnzymologicAnimalsCells, CulturedCluster AnalysisDisease Models, AnimalFibroblastsGene Expression ProfilingImmunohistochemistryIn Situ HybridizationMaleMatrix Metalloproteinase 2MiceMice, Inbred C57BLMicroRNAsMyocardial InfarctionMyocardial Reperfusion InjuryMatrix Metalloproteinase 2MicroRNAsMIRN21 microRNA, mouseMmp2 protein, mouseProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, mouseRNA, Messenger

Identifiers

PMID19147652
PMCPMC2652741
OpenAlexW2097837136

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.