Evidence map›Paper›PMID 29976687›Full record

ReviewCirculation research2018

Extracellular Vesicles and the Application of System Biology and Computational Modeling in Cardiac Repair.

Venkata Naga Srikanth Garikipati, Farnaz Shoja-Taheri, Michael E Davis, Raj Kishore

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

48 citing papers in PubMed, 90 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Inhalable exosomes to target cardiac repair.Extracellular vesicles and circulating nucleic acids · 2025
    Article
  10. Role of Exosomes in Cardiovascular Diseases.Reviews in cardiovascular medicine · 2024
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Deciphering the Cardiovascular Potential of Human CD34International journal of molecular sciences · 2023
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Extracellular Vesicles in Cancer Drug Resistance: Roles, Mechanisms, and Implications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    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

4 authors at 3 institutions in 2 countries.

Venkata Naga Srikanth GarikipatiFrom the Center for Translational Medicine (V.N.S.G., R.K.).
Farnaz Shoja-TaheriLewis Katz School of Medicine, Temple University, Philadelphia, PA; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta (F.S.-T., M.E.D.).
Michael E DavisLewis Katz School of Medicine, Temple University, Philadelphia, PA; Wallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta (F.S.-T., M.E.D.).
Raj KishoreFrom the Center for Translational Medicine (V.N.S.G., R.K.) raj.kishore@temple.edu Michael.davis@bme.emory.edu.
Center for Translational Molecular Medicine · NLGeorgia Institute of Technology · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Small and large animal surgery, physiology and histologyP01HL134608 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI Raj Kishore · 2017 to 2026
$21.0M
TNF mRNA stability and restenosisR01HL091983 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2009 to 2022
$5.3M
Pluripotent cell-derived exosomes as mediators of myocardial regenerationR01HL126186 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2015 to 2018
$1.6M
CPC Excosomes for Cardiac TherapyR56HL124380 · NHLBI · EMORY UNIVERSITY · PI DAVIS, MICHAEL E · 2014 to 2014
$436k
NHLBI NIH HHS P01 HL134608NHLBI NIH HHS R01 HL091983NHLBI NIH HHS R01 HL126186NHLBI NIH HHS R56 HL124380
6 · The paper itself

Abstract

Recent literature suggests that extracellular vesicles (EVs), secreted from most cells and containing cell-specific cargo of proteins, lipids, and nucleic acids, are major driver of intracellular communication in normal physiology and pathological conditions. The recent evidence on stem/progenitor cell EVs as potential therapeutic modality mimicking their parental cell function is exciting because EVs could possibly be used as a surrogate for the stem cell-based therapy, and this regimen may overcome certain roadblocks identified with the use of stem/progenitor cell themselves. This review provides a comprehensive update on our understanding on the role of EVs in cardiac repair and emphasizes the applications of stem/progenitor cell-derived EVs as therapeutics and discusses the current challenges associated with the EV therapy.

Indexed as

AnimalsCardiovascular DiseasesExtracellular VesiclesHumansMicroRNAsStem Cell TransplantationSystems BiologyMicroRNAsbiologyexosomesextracellular vesicleslipidsstem cells

Identifiers

PMID29976687
PMCPMC6512976
OpenAlexW2829895505

What OpenQuestion holds

Textmetadata
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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.