Evidence map›Paper›PMID 42157878›Full record

ArticleInternational journal of general medicine2026

Identification of Key Genes and Exploration of Therapeutic Targets for Chronic Tendon Injury Based on Bioinformatics and Machine Learning.

Zishen Cheng, Weina Ren, Yuqing Wang, Huidong Zhao, Liangliang Jiang, Xiaopeng Pu, Yaxing Zhang, Yantao Wang, Qiangjun Kang

Abstract read
In one paragraph

Article in International journal of general medicine, 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

9 authors.

Zishen Cheng *Department of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Weina Ren *Department of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Yuqing WangDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Huidong ZhaoDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Liangliang JiangDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Xiaopeng PuDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Yaxing ZhangDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Yantao WangDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.
Qiangjun KangDepartment of Orthopaedics, Bethune International Peace Hospital, Shijiazhuang, 050082, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic tendon injury (CTI) is a common musculoskeletal disorder with complex molecular mechanisms, and currently lacks effective targeted therapeutic strategies. A comprehensive analysis of its key pathogenic genes and regulatory networks is crucial for the precise diagnosis and treatment of CTI. Methods: Differentially expressed genes (DEGs) in CTI and normal tendon tissue were identified using the GEO database, and intersected with genes derived from WGCNA to identify candidate genes. Subsequently, functional enrichment analysis was performed, and four machine learning algorithms were employed to further determine key genes. Finally, a systematic functional analysis of the key genes was performed, including assessments of diagnostic value, regulatory network construction, computational drug prediction and molecular docking. Results: A total of 271 candidate genes were identified, which were significantly enriched in focal adhesion, ECM-receptor interaction, and p53 signaling pathway. Subsequently, three key genes ( Conclusion: This study systematically revealed three key genes in CTI through comprehensive bioinformatics analysis. The diagnostic model, regulatory network, and predicted targeted drugs constructed based on these findings laid a solid theoretical foundation for subsequent translational medical research.

Indexed as

bioinformatic analysischronic tendon injurymachine learningnatural killer T cellsTF-mRNA-miRNA molecular network

Identifiers

PMID42157878
PMCPMC13182836

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.