Evidence map›Paper›PMID 33003617›Full record

ReviewBiomolecules2020

Large Animal Models of Cell-Free Cardiac Regeneration.

Andreas Spannbauer, Julia Mester-Tonczar, Denise Traxler, Nina Kastner, Katrin Zlabinger, Ena Hašimbegović, Martin Riesenhuber, Noemi Pavo, Georg Goliasch, Mariann Gyöngyösi

Abstract readReview
In one paragraph

Review in Biomolecules, 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
–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

15 citing papers in PubMed.

  1. Review
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  15. New Developments in Exosomal lncRNAs in Cardiovascular Diseases.Frontiers in cardiovascular medicine · 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.

Andreas SpannbauerCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-9819-0361
Julia Mester-TonczarCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-1426-6670
Denise TraxlerCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0001-8679-1525
Nina KastnerCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-1576-9029
Katrin ZlabingerCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-3855-7643
Ena HašimbegovićCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.
Martin RiesenhuberCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-5061-7354
Noemi PavoCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.
Georg GoliaschCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.
Mariann GyöngyösiCardiology, Department of Medicine II, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-7083-2107

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The adult mammalian heart lacks the ability to sufficiently regenerate itself, leading to the progressive deterioration of function and heart failure after ischemic injuries such as myocardial infarction. Thus far, cell-based therapies have delivered unsatisfactory results, prompting the search for cell-free alternatives that can induce the heart to repair itself through cardiomyocyte proliferation, angiogenesis, and advantageous remodeling. Large animal models are an invaluable step toward translating basic research into clinical applications. In this review, we give an overview of the state-of-the-art in cell-free cardiac regeneration therapies that have been tested in large animal models, mainly pigs. Cell-free cardiac regeneration therapies involve stem cell secretome- and extracellular vesicles (including exosomes)-induced cardiac repair, RNA-based therapies, mainly regarding microRNAs, but also modified mRNA (modRNA) as well as other molecules including growth factors and extracellular matrix components. Various methods for the delivery of regenerative substances are used, including adenoviral vectors (AAVs), microencapsulation, and microparticles. Physical stimulation methods and direct cardiac reprogramming approaches are also discussed.

Indexed as

Cell-Free SystemAnimalsDisease Models, AnimalHeartHumansMyocardial InfarctionMyocytes, CardiacRegenerationSwinecardiac regenerationcardiac reprogrammingcell-freeexosomesextracellular vesiclesgene therapygrowth factorlarge animal modelmicroRNAporcine

Identifiers

PMID33003617
PMCPMC7600588

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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.