# Identification of SDC4 as a potential target for obesity via integrated analysis of the lncRNA-miRNA-mRNA network in visceral adipose tissue

**Authors:** Yuancheng Shao, Feng Ju, Jun Qian, Liming Tang, Shuai Chen

PMC · DOI: 10.1080/21623945.2025.2583542 · Adipocyte · 2025-11-06

## TL;DR

This study identifies SDC4 as a potential target for obesity by analyzing RNA interactions in fat tissue.

## Contribution

The study introduces SDC4 as a novel potential therapeutic target for obesity through an integrated RNA network analysis.

## Key findings

- 118, 92, and 227 differentially expressed lncRNAs, miRNAs, and mRNAs were identified in obese individuals.
- SDC4 was found to be significantly upregulated in obese subjects and correlated with BMI and triglyceride levels.

## Abstract

Obesity is a major global health issue. This study aimed to elucidate its molecular mechanisms by analysing the expression of lncRNAs, miRNAs, and mRNAs in visceral adipose tissue. Through integrated transcriptome sequencing and bioinformatics analysis of obese and normal groups, we observed 118, 92 and 227 differentially expressed lncRNAs, miRNAs and mRNAs, respectively. Functional enrichment analysis revealed these genes were primarily involved in immune response and inflammation-related pathways. A competing endogenous RNA (ceRNA) network was constructed, identifying key interactions among five target genes, including SDC4. Validation confirmed SDC4 was significantly upregulated in obese subjects, and this expression level positively correlated with body mass index and triglyceride. These findings suggest that SDC4 offers the possibility of being a therapeutic target for obesity.

## Linked entities

- **Genes:** SDC4 (syndecan 4) [NCBI Gene 6385]
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** SDC4 (syndecan 4) [NCBI Gene 6385] {aka SYND4}
- **Diseases:** inflammation (MESH:D007249), Obesity (MESH:D009765)
- **Chemicals:** triglyceride (MESH:D014280)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12599498/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12599498/full.md

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Source: https://tomesphere.com/paper/PMC12599498