Evidence map›Paper›PMID 23727269›Full record

ReviewFree radical biology & medicine2013

Mechanosensitive microRNAs-role in endothelial responses to shear stress and redox state.

Traci Marin, Brendan Gongol, Zhen Chen, Brian Woo, Shankar Subramaniam, Shu Chien, John Y-J Shyy

Abstract readReview
In one paragraph

Review in Free radical biology & medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
–field-weighted citation impact
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

67 citing papers in PubMed.

  1. Article
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  9. Role of blood flow in endothelial functionality: a review.Frontiers in cell and developmental biology · 2023
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  11. Article
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  13. Article
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7 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.

Traci MarinBiomedical Sciences, School of Medicine, University of California at Riverside, Riverside, CA 92521, USA.
Brendan Gongol
Zhen Chen
Brian Woo
Shankar Subramaniam
Shu Chien
John Y-J Shyy

Funding

Systems Biology Analyses for Hemodynamic Regulation of Vascular HomeostasisR01HL108735 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2012 to 2024
$13.4M
Shear Regulation of MicroRNA Transportomes and Targetomes in Vascular HomeostasisR01HL106579 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2011 to 2022
$8.3M
Shear Stress, AMPK, and Endothelial FunctionsR01HL089940 · NHLBI · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI SHYY, JOHN YJ · 2009 to 2013
$1.9M
NHLBI NIH HHS HL106579NHLBI NIH HHS HL108735NHLBI NIH HHS HL89940NHLBI NIH HHS R01 HL089940NHLBI NIH HHS R01 HL106579NHLBI NIH HHS R01 HL108735
6 · The paper itself

Abstract

Endothelial functions are highly regulated by imposed shear stress in vivo. The characteristics of shear stress determine mechanotransduction events that regulate phenotypic outcomes including redox and inflammatory states. Recent data indicate that microRNAs (miRs) in vascular endothelial cells play an essential role in shear stress-regulated endothelial responses. More specifically, atheroprotective pulsatile flow (PS) induces miRs that inhibit mediators of oxidative stress and inflammation while promoting those involved in maintaining vascular homeostasis. Conversely, oscillatory flow (OS) elicits the opposing networks. This is exemplified by the PS-responsive transcription factor Krüppel-like factor 2 (KLF2), which regulates miR expression but is also regulated by OS-sensitive miRs to ultimately regulate the oxidative and inflammatory state of the endothelium. In this review, we outline important findings demonstrating the multifaceted roles of shear stress-regulated miRs in endothelial redox and inflammatory balance. Furthermore, we discuss the use of algorithms in deciphering signaling networks differentially regulated by PS and OS.

Indexed as

Mechanotransduction, CellularEndothelial CellsEndothelium, VascularGene Expression RegulationHumansInflammationKruppel-Like Transcription FactorsMicroRNAsOxidation-ReductionOxidative StressPulsatile FlowStress, MechanicalKLF2 protein, humanKruppel-Like Transcription FactorsMicroRNAsACEAMP-activated protein kinaseAMPKangiotensin-converting enzymeCDK4ChIPchromatin immunoprecipitationc-Jun N-terminal kinasecyclin-dependent kinase 4ECELISAendothelial cellendothelial nitric oxide synthaseEndotheliumeNOSenzyme-linked immunosorbent assayFIRMFramework for the Inference of Regulation by MiRsFree radicalsglutathione peroxidaseGPxHDAChistone deacetylaseICAM-1ILInflammationintegrin α5intercellular adhesion molecule 1interleukinITGA5JNKKLF2Krüppel-like factor 2MAP3K7MEF2microRNAmiRMiRmitogen-activated protein kinase kinase kinase 7myocyte enhancer factor-2NADPH oxidaseNF-κBNOXnuclear factor κ-light-chain-enhancer of activated B cellsOSoscillatory shearOxidative stressp21-activated kinasePAKPSpulsatile shearreactive oxygen speciesRho-associated, coiled-coil-containing protein kinase 1ROCK1ROSShear stresssilent mating type information regulation 2 homolog 1SIRT1SODsuperoxide dismutasethioredoxin-dependent peroxidaseTrxR2vascular cell adhesion protein 1VCAM-1β-transducin repeat-containing E3 ubiquitin protein ligaseβTRC

Identifiers

PMID23727269
PMCPMC3762952

What OpenQuestion holds

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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.