Evidence map›Paper›PMID 31852219›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2020

MicroRNA-144 Silencing Protects Against Atherosclerosis in Male, but Not Female Mice.

Joan Cheng, Angela Cheng, Bethan L Clifford, Xiaohui Wu, Ulf Hedin, Lars Maegdefessel, Nathalie Pamir, Tamer Sallam, Elizabeth J Tarling, Thomas Q de Aguiar Vallim

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  5. Review
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  9. Review
  10. Review
  11. MicroRNAs Regulate Function in Atherosclerosis and Clinical Implications.Oxidative medicine and cellular longevity · 2023
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. MicroRNA-mediated regulation of glucose and lipid metabolism.Nature reviews. Molecular cell biology · 2021
    Review
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

10 authors at 2 institutions in 3 countries.

Joan ChengFrom the Department of Biological Chemistry (J.C., A.C., T.Q.d.A.V.), University of California Los Angeles.
Angela ChengFrom the Department of Biological Chemistry (J.C., A.C., T.Q.d.A.V.), University of California Los Angeles.
Bethan L CliffordDepartment of Medicine (B.L.C., X.W., T.S., E.J.T., T.Q.d.A.V.), University of California Los Angeles.
Xiaohui WuDepartment of Medicine (B.L.C., X.W., T.S., E.J.T., T.Q.d.A.V.), University of California Los Angeles.
Ulf HedinDepartment of Molecular Medicine and Surgery (U.H.), Karolinska Institute, Solna, Sweden.
Lars MaegdefesselDepartment of Medicine (L.M.), Karolinska Institute, Solna, Sweden.
Nathalie PamirDepartment of Medicine, Knight Cardiovascular Institute, Oregon Health & Sciences University, Portland (N.P.).
Tamer SallamDepartment of Medicine (B.L.C., X.W., T.S., E.J.T., T.Q.d.A.V.), University of California Los Angeles.
Elizabeth J TarlingDepartment of Medicine (B.L.C., X.W., T.S., E.J.T., T.Q.d.A.V.), University of California Los Angeles.
Thomas Q de Aguiar VallimFrom the Department of Biological Chemistry (J.C., A.C., T.Q.d.A.V.), University of California Los Angeles.
University of California, Los Angeles · USKarolinska Institutet · SE

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Systems genomics of metabolic syndrome traitsP01HL028481 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DAVIS, RICHARD C · 1985 to 2019
$50.2M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MILES Frome WILKINSON · 2003 to 2026
$40.4M
RNA-binding proteins in atherosclerosisR01HL139549 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Tamer Sallam · 2018 to 2026
$3.3M
Novel FXR-dependent Molecular Mechanisms in the Regulation of Liver MetabolismR01DK118064 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EDWARDS, PETER A, VALLIM, THOMAS A · 2019 to 2022
$2.1M
Post-Translational Regulation of Lipid MetabolismR01HL136543 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TARLING, ELIZABETH JOANNA · 2017 to 2021
$1.9M
Transcriptional control of microRNAs in lipid metabolism and atherosclerosisR01HL122677 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI VALLIM, THOMAS A · 2016 to 2020
$1.9M
Long Non-coding RNAs in the Regulation of Adipogenesis and ObesityR01DK118086 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SALLAM, TAMER · 2018 to 2022
$1.9M
Novel Post-Transcriptional Regulators of Lipid MetabolismR01DK112119 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI VALLIM, THOMAS A · 2017 to 2020
$1.7M
Novel transcriptional regulators of bile acid metabolism and hepatotoxicityR01DK102559 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EDWARDS, PETER A · 2014 to 2017
$1.3M
Role of ABCG1 in lipid homeostasis, inflammation and innate immunityR00HL118161 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TARLING, ELIZABETH JOANNA · 2015 to 2017
$740k
NCATS NIH HHS UL1 TR000124NHLBI NIH HHS K99 HL118161NHLBI NIH HHS P01 HL028481NHLBI NIH HHS R00 HL118161NHLBI NIH HHS R01 HL122677NHLBI NIH HHS R01 HL136543NHLBI NIH HHS R01 HL139549NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK102559NIDDK NIH HHS R01 DK112119NIDDK NIH HHS R01 DK118064NIDDK NIH HHS R01 DK118086
6 · The paper itself

Abstract

objectiveAtherosclerosis is a leading cause of death in developed countries. MicroRNAs act as fine-tuners of gene expression and have been shown to have important roles in the pathophysiology and progression of atherosclerosis. We, and others, previously demonstrated that microRNA-144 (miR-144) functions to post-transcriptionally regulate ABCA1 (ATP binding cassette transporter A1) and plasma HDL (high-density lipoprotein) cholesterol levels. Here, we explore how miR-144 inhibition may protect against atherosclerosis. Approach and Results: We demonstrate that miR-144 silencing reduced atherosclerosis in male, but not female low-density lipoprotein receptor null (

conclusionsOur data demonstrate silencing miR-144 has sex-specific effects and that treatment with antisense oligonucleotides to target miR-144 might result in enhancements in reverse cholesterol transport and oxysterol metabolism in patients with cardiovascular disease.

Indexed as

Gene SilencingAnimalsAtherosclerosisBlotting, WesternCholesterolDisease Models, AnimalFemaleMaleMiceMice, KnockoutMicroRNAsRNASex FactorsCholesterolMicroRNAsMIRN144 microRNA, mouseRNAantisense oligonucleotidesatherosclerosiscardiovascular diseasecholesterolmicroRNA

Identifiers

PMID31852219
PMCPMC7018399
OpenAlexW2996582458

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.