Evidence map›Paper›PMID 41278551›Full record

ArticleInternational journal of genomics2025

Discovery Potential Hub Genes and Pathways in Keloid Fibroblast Development Based on Bioinformatics Analysis.

Boao Zhao, Wei Zhang, Wende Yao, Xinyi Li, Tao Yang, Hui Cheng, Xiaojing Li

Abstract read
In one paragraph

Article in International journal of genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Boao ZhaoDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0009-0008-6373-7794
Wei ZhangDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0000-0002-4032-0768
Wende YaoDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0009-0005-5454-4710
Xinyi LiDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0009-0007-5403-4432
Tao YangDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0009-0006-1677-1936
Hui ChengDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0009-0007-0226-4287
Xiaojing LiDepartment of Plastic Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China, ahmu.edu.cn.ORCID https://orcid.org/0000-0002-2609-0572

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Keloid is a common pathological scar tissue, which invades the surrounding normal skin and leads to symptoms such as pain, pruritus, erythema, and edema, thereby impacting the quality of life. In this study, we conducted bioinformatics analysis of keloid fibroblasts and normal skin tissue to identify DEGs and the pathways involved in the mechanism of keloid fibroblast proliferation. Methods: GSE145725 was downloaded from the Gene Expression Omnibus (GEO) database, including nine keloid fibroblasts and 10 normal tissue fibroblast samples. GSE158395 included four lesional and three nonlesional samples from keloid patients, and six normal skin tissue samples were also evaluated. Through bioinformatics analysis, we established diagnosis model, and at the same time, we predicted therapeutic targets in the DSigDB database. Results: Six key genes were screened out by bioinformatics analysis, including BMP4, SPP1, HIF1 Conclusions: This study identified three hub genes-BMP4, POSTN, and WNT5A-that are closely linked to keloid fibroblast hyperplasia and may serve as potential biomarkers for inhibiting keloid fibroblast hyperplasia. Further molecular and animal studies are needed to fully understand the mechanisms of keloid development.

Indexed as

bioinformaticsGEOhub geneskeloid

Identifiers

PMID41278551
PMCPMC12635863

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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.