Evidence map›Paper›PMID 35110584›Full record

ArticleNPJ Regenerative medicine2022

CDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cells.

Julia Junghof, Yuta Kogure, Tian Yu, Eva María Verdugo-Sivianes, Megumi Narita, Antonio Lucena-Cacace, Yoshinori Yoshida

Open access · goldAbstract read
In one paragraph

Article in NPJ Regenerative medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Epicardium-myocardium crosstalk orchestrates heart development.Frontiers in cell and developmental biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. LncRNAs in theInternational journal of molecular sciences · 2024
    Article
  14. Epicardial EMT and cardiac repair: an update.Stem cell research & therapy · 2024
    Review
  15. Genomic structural variation contributes to evolved changes in gene expression in high-altitude Tibetan sheep.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. 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

7 authors at 2 institutions in 2 countries.

Julia JunghofCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.ORCID http://orcid.org/0000-0002-2674-4361
Yuta KogureCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Tian YuCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Eva María Verdugo-SivianesInstituto de Biomedicina de Sevilla, IBIS, Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Consejo Superior de Investigaciones Científicas, Avda. Manuel Siurot s/n, 41013, Seville, Spain.ORCID http://orcid.org/0000-0002-0922-0371
Megumi NaritaCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.ORCID http://orcid.org/0000-0002-8198-4042
Antonio Lucena-CacaceCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan. a.lucena@cira.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-1181-2683
Yoshinori YoshidaCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan. yoshinor@cira.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0001-5511-9090
Kyoto University · JPConsejo Superior de Investigaciones Científicas · ES

Funding

Fondation Leducq 18CVD05Japan Agency for Medical Research and Development (AMED) JP19bk0104095Japan Agency for Medical Research and Development (AMED) JP19bm0104001Japan Agency for Medical Research and Development (AMED) JP19bm0804008Japan Agency for Medical Research and Development (AMED) JP19mk0104117Japan Agency for Medical Research and Development (AMED) JP20bm0204003Japan Agency for Medical Research and Development (AMED) JP20bm0804022MEXT | Japan Society for the Promotion of Science (JSPS) 17H04176MEXT | Japan Society for the Promotion of Science (JSPS) 20K17078MEXT | Japan Society for the Promotion of Science (JSPS) 21H02912
6 · The paper itself

Abstract

The epicardium is a mesothelial layer covering the myocardium serving as a progenitor source during cardiac development. The epicardium reactivates upon cardiac injury supporting cardiac repair and regeneration. Fine-tuned balanced signaling regulates cell plasticity and cell-fate decisions of epicardial-derived cells (EPCDs) via epicardial-to-mesenchymal transition (EMT). However, powerful tools to investigate epicardial function, including markers with pivotal roles in developmental signaling, are still lacking. Here, we recapitulated epicardiogenesis using human induced pluripotent stem cells (hiPSCs) and identified type II classical cadherin CDH18 as a biomarker defining lineage specification in human active epicardium. The loss of CDH18 led to the onset of EMT and specific differentiation towards cardiac smooth muscle cells. Furthermore, GATA4 regulated epicardial CDH18 expression. These results highlight the importance of tracing CDH18 expression in hiPSC-derived epicardial cells, providing a model for investigating epicardial function in human development and disease and enabling new possibilities for regenerative medicine.

Identifiers

PMID35110584
PMCPMC8810917
OpenAlexW4210480240

What OpenQuestion holds

Textmetadata
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.