Evidence map›Paper›PMID 42521489›Full record

ArticleInternational journal of stem cells2026

CXCL14 Enhances Myocyte Fusion and Activates the FAK-ERK5 Signaling Pathway in Skeletal Muscle Stem Cells and Myoblasts.

Nurkyz Alymkulova, Younjeong Oh, Jennifer Fransisca, Bagus Sarmito, Yongsung Hwang, Jeong Kyo Yoon

Abstract read
In one paragraph

Article in International journal of stem cells, 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

6 authors.

Nurkyz AlymkulovaDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0009-0008-8515-6640
Younjeong OhDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0009-0007-6501-2626
Jennifer FransiscaDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0009-0002-0140-7120
Bagus SarmitoDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0009-0009-8461-4045
Yongsung HwangDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0000-0001-5558-5171
Jeong Kyo YoonDepartment of Integrated Biomedical Science, Graduate School, Soonchunhyang University, Cheonan, Korea.ORCID https://orcid.org/0000-0002-1355-3806

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal muscle regeneration is essential for maintaining muscle function throughout life and is regulated by numerous growth factors, cytokines and their associated signaling pathways. In this study, we investigated the role of C-X-C motif chemokine ligand 14 (CXCL14) in myogenic differentiation using skeletal muscle stem cells (MuSC) and the mouse myoblast C2C12 cell line. Notably, CXCL14 significantly enhanced myocyte fusion. To elucidate the underlying regulatory mechanisms, we examined fusion-associated signaling pathways and found that CXCL14 activates the focal adhesion kinase-extracellular regulated protein kinase 5 (FAK-ERK5) signaling pathway. Our findings identify the CXCL14-FAK-ERK5 signaling axis as a positive regulator of myocyte fusion. Furthermore, by establishing fibro-adipogenic progenitors (FAPs) as the primary source of CXCL14 and demonstrating its pro-fusion activity, this study provides new insight into the paracrine regulation from FAPs to MuSCs during muscle regeneration.

Indexed as

CXCL14ERK5FAKMuscle regenerationSkeletal muscle satellite cells

Identifiers

PMID42521489
PMCPMC13519543

What OpenQuestion holds

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Registered trials

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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.