Evidence map›Paper›PMID 36232943›Full record

ReviewInternational journal of molecular sciences2022

Multicellular 3D Models for the Study of Cardiac Fibrosis.

Vittorio Picchio, Erica Floris, Yuriy Derevyanchuk, Claudia Cozzolino, Elisa Messina, Francesca Pagano, Isotta Chimenti, Roberto Gaetani

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Dressed in Collagen: 2D and 3D Cardiac Fibrosis Models.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Recent Advances in 3D Cultures.International journal of molecular sciences · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Global hotspots and emerging trends in 3D bioprinting research.Frontiers in bioengineering and biotechnology · 2023
    Article
  14. 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

8 authors.

Vittorio PicchioDepartment of Medical Surgical Sciences and Biotechnologies, Sapienza University, 04100 Latina, Italy.ORCID 0000-0003-1591-5118
Erica FlorisDepartment of Medical Surgical Sciences and Biotechnologies, Sapienza University, 04100 Latina, Italy.
Yuriy DerevyanchukDepartment of Molecular Medicine, Sapienza University, 00161 Rome, Italy.
Claudia CozzolinoDepartment of Medical Surgical Sciences and Biotechnologies, Sapienza University, 04100 Latina, Italy.
Elisa MessinaDepartment of Molecular Medicine, Sapienza University, 00161 Rome, Italy.ORCID 0000-0002-1654-9001
Francesca PaganoInstitute of Biochemistry and Cell Biology, National Council of Research (IBBC-CNR), 00015 Monterotondo, Italy.
Isotta ChimentiDepartment of Medical Surgical Sciences and Biotechnologies, Sapienza University, 04100 Latina, Italy.ORCID 0000-0002-0865-8814
Roberto GaetaniDepartment of Molecular Medicine, Sapienza University, 00161 Rome, Italy.

Funding

Regione Lazio A0375-2020-36621Sapienza University of Rome RG11916B85CDBF76Sapienza University of Rome RM12117A805ED2FD
6 · The paper itself

Abstract

Ex vivo modelling systems for cardiovascular research are becoming increasingly important in reducing lab animal use and boosting personalized medicine approaches. Integrating multiple cell types in complex setups adds a higher level of significance to the models, simulating the intricate intercellular communication of the microenvironment in vivo. Cardiac fibrosis represents a key pathogenetic step in multiple cardiovascular diseases, such as ischemic and diabetic cardiomyopathies. Indeed, allowing inter-cellular interactions between cardiac stromal cells, endothelial cells, cardiomyocytes, and/or immune cells in dedicated systems could make ex vivo models of cardiac fibrosis even more relevant. Moreover, culture systems with 3D architectures further enrich the physiological significance of such in vitro models. In this review, we provide a summary of the multicellular 3D models for the study of cardiac fibrosis described in the literature, such as spontaneous microtissues, bioprinted constructs, engineered tissues, and organs-on-chip, discussing their advantages and limitations. Important discoveries on the physiopathology of cardiac fibrosis, as well as the screening of novel potential therapeutic molecules, have been reported thanks to these systems. Future developments will certainly increase their translational impact for understanding and modulating mechanisms of cardiac fibrosis even further.

Indexed as

Endothelial CellsTissue EngineeringAnimalsCell CommunicationFibrosisMyocytes, Cardiac3D culturescardiac fibroblastscardiac fibrosiscardiac stromal cellsorganoidsorgans-on-chiptissue engineering

Identifiers

PMID36232943
PMCPMC9569892

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.