Evidence map›Paper›PMID 35996406›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Identification of Potential Therapeutic Target Genes in Osteoarthritis.

Yang Hu, Yinteng Wu, Fu Gan, Mingyang Jiang, Dongxu Chen, Mingjing Xie, Yiji Jike, Zhandong Bo

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Yang HuDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Yinteng WuDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Fu GanDepartment of Urology Surgery, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise 533000, China.ORCID https://orcid.org/0000-0001-6165-7952
Mingyang JiangDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Dongxu ChenDepartment of Joint Surgery and Sports Medicine, Nanxishan Hospital of Guangxi Zhuang Autonomous Region, Guilin 541002, China.ORCID https://orcid.org/0000-0002-4357-2653
Mingjing XieDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Yiji JikeDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Zhandong BoDepartment of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.ORCID https://orcid.org/0000-0001-6827-4508
Guangxi Medical University · CNAffiliated Hospital of Youjiang Medical University for Nationalities · CNNanxi Mountain Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Osteoarthritis (OA), also known as joint failure, is characterized by joint pain and, in severe cases, can lead to loss of joint function in patients. Immune-related genes and immune cell infiltration play a crucial role in OA development. We used bioinformatics approaches to detect potential diagnostic markers and available drugs for OA while initially exploring the immune mechanisms of OA. Methods: The training set GSE55235 and validation set GSE51588 and GSE55457 were obtained from the Gene Expression Omnibus (GEO) database and differentially expressed genes (DEGs) were identified by the limma package. Gene set enrichment analysis (GSEA) was performed on the GSE55235 dataset using the cluster profiler package. At the same time, DEGs were analyzed by gene ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG). In addition, protein-protein interaction (PPI) analysis was performed on the common DEGs of the three datasets using the STRING database. Proteins with direct linkage were identified as hub genes, and the relation of hub genes was subsequently analyzed using the GOSemSim package. Hub genes' expression profiles and diagnostic capabilities (ROC curves) were analyzed and validated using three datasets. In addition, we performed RT-qPCR to validate the levels of hub genes. The immune microenvironment was analyzed using the CIBERSORT package, and the relationship between hub genes and immune cells was evaluated. In addition, we used a linkage map (CMAP) database to identify available drug candidates. Finally, the GSEA of hub genes was used to decipher the potential pathways corresponding to hub genes. Results: Three hub genes ( Conclusion: CX3CR1, MYC, and TLR7 are associated with various immune cells and are the potential diagnostic markers and therapeutic targets for OA.

Identifiers

PMID35996406
PMCPMC9392645
OpenAlexW4291247452

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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.