Evidence map›Paper›PMID 31842627›Full record

ArticleHuman gene therapy2020

Exosome-Mediated Transfer of Anti-miR-33a-5p from Transduced Endothelial Cells Enhances Macrophage and Vascular Smooth Muscle Cell Cholesterol Efflux.

Alexis Stamatikos, Ethan Knight, Lucia Vojtech, Lianxiang Bi, Bradley K Wacker, Chongren Tang, David A Dichek

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

39 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  9. Review
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  12. Inhibition of miR-33a-5p in Macrophage-like Cells In Vitro Promotes apoAI-Mediated Cholesterol Efflux.Pathophysiology : the official journal of the International Society for Pathophysiology · 2024
    Article
  13. Article
  14. Review
  15. Apolipoprotein A-I vascular gene therapy reduces vein-graft atherosclerosis.Molecular therapy. Methods & clinical development · 2023
    Article
  16. Article
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  19. Review
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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 at 1 institution in 1 country.

Alexis StamatikosDepartment of Medicine, University of Washington, Seattle, Washington.
Ethan KnightDepartment of Medicine, University of Washington, Seattle, Washington.
Lucia VojtechDepartment of Obstetrics and Gynecology, University of Washington, Seattle, Washington.
Lianxiang BiDepartment of Medicine, University of Washington, Seattle, Washington.
Bradley K WackerDepartment of Medicine, University of Washington, Seattle, Washington.
Chongren TangDepartment of Medicine, University of Washington, Seattle, Washington.
David A DichekDepartment of Medicine, University of Washington, Seattle, Washington.
University of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
CARDIOVASCULAR RESEARCH TRAINING PROGRAMT32HL007828 · NHLBI · UNIVERSITY OF WASHINGTON · PI Francis Kim, Farid Moussavi-Harami · 1997 to 2026
$10.2M
Atheroprotective Gene TherapyR01HL114541 · NHLBI · UNIVERSITY OF WASHINGTON · PI DICHEK, DAVID A · 2013 to 2022
$4.9M
NCI NIH HHS P30 CA015704NHLBI NIH HHS R01 HL114541NHLBI NIH HHS T32 HL007828
6 · The paper itself

Abstract

Atherosclerosis is a disease of large- and medium-sized arteries that is caused by cholesterol accumulation in arterial intimal cells, including macrophages and smooth muscle cells (SMC). Cholesterol accumulation in these cells can be prevented or reversed in preclinical models-and atherosclerosis reduced-by transgenesis that increases expression of molecules that control cholesterol efflux, including apolipoprotein AI (apoAI) and ATP-binding cassette subfamily A, member 1 (ABCA1). In a previous work, we showed that transduction of arterial endothelial cells (EC)-with a helper-dependent adenovirus (HDAd) expressing apoAI-enhanced EC cholesterol efflux

Indexed as

RNA InterferenceAntagomirsApolipoprotein A-IATP Binding Cassette Transporter 1Biological TransportCholesterolEndothelial CellsExosomesExtracellular VesiclesHumansMacrophagesMicroRNAsMyocytes, Smooth MuscleRNA, Small UntranslatedRNA TransportABCA1 protein, humanAntagomirsAPOA1 protein, humanApolipoprotein A-IATP Binding Cassette Transporter 1CholesterolMicroRNAsMIRN33a microRNA, humanRNA, Small UntranslatedantagomiRscholesterol effluxendothelial cellsexosomeshelper-dependent adenovirus

Identifiers

PMID31842627
PMCPMC7047121
OpenAlexW2996273488

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.