Evidence map›Paper›PMID 25012134›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2014

Role of flow-sensitive microRNAs in endothelial dysfunction and atherosclerosis: mechanosensitive athero-miRs.

Sandeep Kumar, Chan Woo Kim, Rachel D Simmons, Hanjoong Jo

Open access · bronzeAbstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed
8.2field-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

156 citing papers in PubMed, 267 citations in OpenAlex.

  1. Review
  2. Systemic Molecular Alterations ofInternational journal of molecular sciences · 2026
    Article
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96 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

4 authors at 1 institution in 1 country.

Sandeep KumarFrom the Wallace H. Coulter Department of Biomedical Engineering (S.K., C.W.K., R.D.S., H.J.) and Division of Cardiology (H.J.), Georgia Institute of Technology and Emory University, Atlanta, GA.
Chan Woo KimFrom the Wallace H. Coulter Department of Biomedical Engineering (S.K., C.W.K., R.D.S., H.J.) and Division of Cardiology (H.J.), Georgia Institute of Technology and Emory University, Atlanta, GA.
Rachel D SimmonsFrom the Wallace H. Coulter Department of Biomedical Engineering (S.K., C.W.K., R.D.S., H.J.) and Division of Cardiology (H.J.), Georgia Institute of Technology and Emory University, Atlanta, GA.
Hanjoong JoFrom the Wallace H. Coulter Department of Biomedical Engineering (S.K., C.W.K., R.D.S., H.J.) and Division of Cardiology (H.J.), Georgia Institute of Technology and Emory University, Atlanta, GA. hanjoong.jo@bme.gatech.edu.
The Wallace H. Coulter Department of Biomedical Engineering · US

Funding

T cell triggering events and hypertensionP01HL095070 · NHLBI · EMORY UNIVERSITY · PI JO, HANJOONG · 2009 to 2019
$20.5M
Shear stress, endothelial miRNAs, and AV calcificationR01HL119798 · NHLBI · EMORY UNIVERSITY · PI JO, HANJOONG, YOGANATHAN, AJIT P · 2013 to 2022
$4.7M
Metabolomics of subclinical and clinical cardiovascular diseaseP20HL113451 · NHLBI · EMORY UNIVERSITY · PI JONES, DEAN PAUL · 2012 to 2016
$4.3M
Graduate Training for Rationally Designed, Integrative Biomaterials - GT BioMATT32EB006343 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI TEMENOFF, JOHNNA S · 2008 to 2018
$2.2M
NHLBI NIH HHS HHSN268201000043CNHLBI NIH HHS HL095070NHLBI NIH HHS HL113451NHLBI NIH HHS HL114772NHLBI NIH HHS P01 HL095070NHLBI NIH HHS P20 HL113451NHLBI NIH HHS R01 HL119798NIBIB NIH HHS T32 EB006343
6 · The paper itself

Abstract

Atherosclerosis preferentially occurs in arterial regions exposed to disturbed flow, in part, due to alterations in gene expression. MicroRNAs (miRNAs) are small, noncoding genes that post-transcriptionally regulate gene expression by targeting messenger RNA transcripts. Emerging evidence indicates that alteration of flow conditions regulate expression of miRNAs in endothelial cells both in vitro and in vivo. These flow-sensitive miRNAs, known as mechano-miRs, regulate endothelial gene expression and can regulate endothelial dysfunction and atherosclerosis. MiRNAs such as, miR-10a, miR-19a, miR-23b, miR-17-92, miR-21, miR-663, miR-92a, miR-143/145, miR-101, miR-126, miR-712, miR-205, and miR-155, have been identified as mechano-miRs. Many of these miRNAs were initially identified as flow sensitive in vitro and were later found to play a critical role in endothelial function and atherosclerosis in vivo through either gain-of-function or loss-of-function approaches. The key signaling pathways that are targeted by these mechano-miRs include the endothelial cell cycle, inflammation, apoptosis, and nitric oxide signaling. Furthermore, we have recently shown that the miR-712/205 family, which is upregulated by disturbed flow, contributes to endothelial inflammation and vascular hyperpermeability by targeting tissue inhibitor of metalloproteinase-3, which regulates metalloproteinases and a disintegrin and metalloproteinases. The mechano-miRs that are implicated in atherosclerosis are termed as mechanosensitive athero-miRs and are potential therapeutic targets to prevent or treat atherosclerosis. This review summarizes the current knowledge of mechanosensitive athero-miRs and their role in vascular biology and atherosclerosis.

Indexed as

Mechanotransduction, CellularAnimalsAtherosclerosisEndothelial CellsEndothelium, VascularGene Expression RegulationHemodynamicsHumansMicroRNAsRegional Blood FlowStress, MechanicalMicroRNAsatherosclerosismatrix metalloproteinasesmicroRNAs

Identifiers

PMID25012134
PMCPMC4169332
OpenAlexW2118891188

What OpenQuestion holds

Textmetadata
LicenceTDM
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.