Evidence map›Paper›PMID 41684555›Full record

ArticleArchives of medical science : AMS2025

Unveiling the immune-related ceRNA network in osteoarthritis: key biomarkers and therapeutic targets.

Jia-Qi Shi, Li Chen, Xu Wang, Xin Ma

Abstract read
In one paragraph

Article in Archives of medical science : AMS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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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

4 authors.

Jia-Qi ShiDepartment of Orthopedic, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Li ChenDepartment of Orthopedic, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Xu WangDepartment of Orthopedic, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Xin MaDepartment of Orthopedic, Huashan Hospital Affiliated to Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The aim of this study was to explore the immune-related competitive endogenous RNA (ceRNA) network in osteoarthritis (OA), focusing on identifying differentially expressed long non-coding RNAs (lncRNAs), constructing a classification model, and examining the associations between these lncRNAs and immune cell subsets in OA. Material and methods: Microarray data from the Gene Expression Omnibus (GEO) database were used to identify differentially expressed genes (DEGs) in synovial tissue of OA patients. A classification model was constructed using the Least Absolute Shrinkage and Selection Operator (LASSO) regression with selected lncRNAs. Computational methods such as CIBERSORT were employed to quantify immune cell infiltration patterns, and weighted gene co-expression network analysis (WGCNA) was conducted to delineate co-expression modules. Finally, a ceRNA network was constructed to elucidate the regulatory interactions among lncRNAs, miRNAs, and mRNAs. Results: We identified 5927 DEGs, among which 47 were differentially expressed long non-coding RNAs (DELs). Seven DELs (DGCR11, FAM215A, HCG9, PART1, FAM106A, NOP14-AS1, PRORY) formed the basis of a classification model with an area under the receiver operating characteristic (ROC) curve of 1. We also examined the infiltration patterns of immune cells in OA tissues and found significant differences compared to healthy controls, indicating a strong immunological component in OA pathogenesis. WGCNA identified a turquoise module showing a strong correlation with OA traits. Conclusions: The study highlights the importance of ceRNA networks in understanding the complex pathogenesis of OA and offers a comprehensive framework for future research into potential diagnostic biomarkers and therapeutic targets.

Indexed as

biomarkerscompetitive endogenous RNAimmune cell infiltrationlong non-coding RNAosteoarthritistherapeutic targets

Identifiers

PMID41684555
PMCPMC12892265

What Socratic holds

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