Evidence map›Paper›PMID 42256527›Full record

ArticleJournal of cell communication and signaling2026

Species-specific roles of cellular communication network proteins in cartilage development: A comparative study using in vitro chondrogenic models.

Zhangzheng Wang, Judit Vágó, Roland Takács, Szilárd Póliska, Ee Hyun Kim, Eun-Jung Jin, Satoshi Kubota, Celina G Kleer, Bernard Perbal, Csaba Matta

Abstract read
In one paragraph

Article in Journal of cell communication and signaling, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zhangzheng WangDepartment of Anatomy, Histology and Embryology Faculty of Medicine University of Debrecen Debrecen Hungary.ORCID https://orcid.org/0000-0003-3871-5143
Judit VágóDepartment of Anatomy, Histology and Embryology Faculty of Medicine University of Debrecen Debrecen Hungary.ORCID https://orcid.org/0000-0003-4379-6734
Roland TakácsDepartment of Anatomy, Histology and Embryology Faculty of Medicine University of Debrecen Debrecen Hungary.ORCID https://orcid.org/0000-0002-1598-3922
Szilárd PóliskaGenomic Medicine and Bioinformatics Core Facility Department of Biochemistry and Molecular Biology Faculty of Medicine University of Debrecen Debrecen Hungary.ORCID https://orcid.org/0000-0002-9722-251X
Ee Hyun KimDepartment of Biomedical Materials Science Graduate School of JABA Wonkwang University Iksan Republic of Korea.ORCID https://orcid.org/0009-0001-5013-9313
Eun-Jung JinDepartment of Biomedical Materials Science Graduate School of JABA Wonkwang University Iksan Republic of Korea.ORCID https://orcid.org/0000-0002-6874-3017
Satoshi KubotaDepartment of Biochemistry and Molecular Dentistry Okayama University, Faculty of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.ORCID https://orcid.org/0000-0003-0795-5072
Celina G KleerDepartment of Pathology University of Michigan Medical School Ann Arbor Michigan USA.ORCID https://orcid.org/0000-0001-8195-185X
Bernard PerbalInternational CCN Society Nice France.ORCID https://orcid.org/0000-0002-6517-2669
Csaba MattaDepartment of Anatomy, Histology and Embryology Faculty of Medicine University of Debrecen Debrecen Hungary.ORCID https://orcid.org/0000-0002-9678-7420

Funding

Role of EZH2 in Breast Cancer ProgressionR01CA107469 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Celina G Kleer · 2005 to 2026
$5.9M
Role of CCN6 (WISP3) in the Progression and Metastasis of Breast Cancer.R01CA125577 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Celina G Kleer · 2008 to 2026
$5.5M
NCI NIH HHS R01 CA107469NCI NIH HHS R01 CA125577
6 · The paper itself

Abstract

Cellular communication network (CCN) proteins are key matricellular regulators of cartilage development, yet their species-specific roles and network-level context remain unclear. This study integrated bulk RNA sequencing from chicken and mouse embryonic limb bud micromass cultures and human mesenchymal stem cell chondrogenesis with co-expression, protein-protein interaction, and ortholog analyses to construct CCN-centered regulatory networks across models. CCN1 and CCN2 emerged as dominant, conserved hubs enriched in collagen-containing extracellular matrix, cartilage development, and growth factor signaling modules, whereas CCN3-CCN6 showed lower context-dependent expression and connectivity. Functional and ortholog analyses revealed moderate pathway conservation, with high conservation of IGF, EGFR, and HIF-1 signaling, but reduced overlap in hypoxia and mechanosensing/Hippo categories, indicating species-specific tuning of environmental sensing. A focused ortholog screen identified multifunctional conserved hubs, including

Indexed as

cartilage regenerationCCNchondrogenesisosteoarthritisregulatory networktranscriptomics

Identifiers

PMID42256527
PMCPMC13240526

What OpenQuestion holds

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LicenceCC BY
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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.