Evidence map›Paper›PMID 32485073›Full record

ArticleJournal of cellular and molecular medicine2020

Analysis of extracellular vesicle miRNA profiles in heart failure.

Jae Gyun Oh, Philyoung Lee, Ronald E Gordon, Susmita Sahoo, Changwon Kho, Dongtak Jeong

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  8. Review
  9. Updated Methods of Extracellular Vesicles Isolation.Advances in experimental medicine and biology · 2023
    Article
  10. Review
  11. Article
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  14. Article
  15. Analysis of extracellular vesicle miRNA profiles in heart failure.Journal of cellular and molecular medicine · 2020
    Article
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

6 authors at 2 institutions in 2 countries.

Jae Gyun OhCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Philyoung LeeCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Ronald E GordonPathology Department, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Susmita SahooCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Changwon KhoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Dongtak JeongCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0003-4153-3498
Icahn School of Medicine at Mount Sinai · USPusan National University · KR

Funding

Extracellular Vesicle-Encapsulated AAVs for Therapeutic Gene Delivery to the HeartR01HL148786 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kiyotake Ishikawa, Susmita Sahoo · 2019 to 2026
$4.1M
Therapeutic Mechanisms of Human CD34 ExosomesR01HL124187 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SAHOO, SUSMITA · 2014 to 2018
$2.1M
Dysregulated Adenosine Methylation of mRNA as a Novel Mechanism of Heart FailureR01HL140469 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SAHOO, SUSMITA · 2018 to 2021
$1.7M
American Heart Association-American Stroke Association 18TPA34170460NHLBI NIH HHS R01 HL124187NHLBI NIH HHS R01 HL140469NHLBI NIH HHS R01 HL148786
6 · The paper itself

Abstract

Extracellular vesicles (EVs) have recently emerged as an important carrier for various genetic materials including microRNAs (miRs). Growing evidences suggested that several miRs transported by EVs were particularly involved in modulating cardiac function. However, it has remained unclear what miRs are enriched in EVs and play an important role in the pathological condition. Therefore, we established the miR expression profiles in EVs from murine normal and failing hearts and consecutively identified substantially altered miRs. In addition, we have performed bioinformatics approach to predict potential cardiac outcomes through the identification of miR targets. Conclusively, we observed approximately 63% of predicted targets were validated with previous reports. Notably, the predicted targets by this approach were often involved in both beneficial and malicious signalling pathways, which may reflect heterogeneous cellular origins of EVs in tissues. Lastly, there has been an active debate on U6 whether it is a proper control. Through further analysis of EV miR profiles, miR-676 was identified as a superior reference control due to its consistent and abundant expressions. In summary, our results contribute to identifying specific EV miRs for the potential therapeutic targets in heart failure and suggest that miR-676 as a new reference control for the EV miR studies.

Indexed as

Gene Expression ProfilingAnimalsDown-RegulationExtracellular VesiclesHeart FailureMaleMice, Inbred C57BLMicroRNAsProteomicsReproducibility of ResultsUp-RegulationMicroRNAsbioinformaticsextracellular vesicleheart failuremicroRNAmicroRNA arraymicroRNA controlmiR-676U6

Identifiers

PMID32485073
PMCPMC7339231
OpenAlexW3031767553

What OpenQuestion holds

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LicenceCC BY
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.