Evidence map›Paper›PMID 29987817›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2018

Cardiac Tissue Engineering Models of Inherited and Acquired Cardiomyopathies.

Irene C Turnbull, Joshua Mayourian, Jack F Murphy, Francesca Stillitano, Delaine K Ceholski, Kevin D Costa

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2018. 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
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Engineering and Assessing Cardiac Tissue Complexity.International journal of molecular sciences · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. 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

6 authors.

Irene C TurnbullCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Joshua MayourianCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jack F MurphyCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Francesca StillitanoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Delaine K CeholskiCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Kevin D CostaCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA. kevin.costa@mssm.edu.

Funding

Harnessing Paracrine Mechanisms of Stem Cell-mediated Cardiac Contractile EnhancementR01HL132226 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI COSTA, KEVIN D · 2017 to 2020
$1.7M
Harnessing the Benefits of Adult Stem Cell Exosomes for Enhancing Cardiac Contractile FunctionK01HL133424 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAL Y MAYOR-TURNBULL, IRENE · 2016 to 2020
$701k
The Role of Exosomes in Mesenchymal Stem Cell-Mediated Enhancement of Cardiac ContractilityF30HL134283 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MAYOURIAN, JOSHUA · 2017 to 2018
$81k
American Heart Association-American Stroke Association 15POST25090116NHLBI NIH HHS F30 HL134283NHLBI NIH HHS K01 HL133424NHLBI NIH HHS R01 HL132226
6 · The paper itself

Abstract

The lack of biomimetic in vitro models of the human heart has posed a critical barrier to progress in the field of modeling cardiac disease. Human engineered cardiac tissues (hECTs)-autonomous, beating structures that recapitulate key aspects of native cardiac muscle physiology-offer an attractive alternative to traditional in vitro models. Here we describe the use of hECTs to advance our understanding and modeling of cardiac diseases in order to test therapeutic interventions, with a focus on contractile dysfunction in the setting of inherited and acquired forms of cardiomyopathies. Four major procedures are discussed in this chapter: (1) preparation of hECTs from human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) on single-tissue and multitissue bioreactors; (2) data acquisition of hECT contractile function on both of these platforms; (3) hECT modeling of hereditary phospholamban-R14 deletion-dilated cardiomyopathy; and (4) cryo-injury and doxorubicin-induced hECT models of acquired cardiomyopathy.

Indexed as

Cell DifferentiationBioreactorsCardiomyopathiesCardiomyopathy, DilatedDoxorubicinEquipment DesignFreezingHumansInduced Pluripotent Stem CellsMyocardial ContractionMyocardiumMyocytes, CardiacTissue EngineeringDoxorubicinAcquired cardiomyopathyContractilityGenetic cardiomyopathyModels of diseaseStem cellsTissue engineering

Identifiers

PMID29987817
PMCPMC6561092

What OpenQuestion holds

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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.