在贫血糖尿病足的LncRNA和mRNA表达特征和生物信息分析
Jiayu Lin1, Jingying Wang1, Bo Liang1
1Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian, China.
Frontiers in genetics
|October 14, 2025
概括
这项研究揭示了糖尿病足 (DFU) 中的新型长非编码RNA (lncRNA) -信使RNA (mRNA) 网络与血红蛋白缺乏相关. 这些网络突出突出破坏铁代谢和炎症,为贫血的DFU提供潜在的诊断标记.
科学领域:
- 生物化学 生化学
- 基因组学就是基因组学.
- 分子生物学分子生物学
背景情况:
- 糖尿病足 (DFU) 是一种严重的并发症,通常与血红蛋白缺乏有关.
- 转录基因变化与DFU的发病有关,但长非编码RNAs (lncRNAs) 在将血红蛋白异常与铁炎症失调联系中的作用尚不清楚.
研究的目的:
- 确定与铁代谢和炎症相关的DFU特定的lncRNA-mRNA联合表达网络.
- 评估这些网络在DFU患者中的诊断潜力.
主要方法:
- 在DFU患者和对照患者的皮肤组织上进行了RNA测序.
- 使用DESeq2.2识别了差异表达的lncRNA和mRNA.
- 用基因组丰富分析 (GSEA) 和共同表达网络构建来分析功能途径和相互作用.
主要成果:
- 在DFU组织中发现了21种差异表达的lncRNA和368种差异表达的mRNA.
- GSEA揭示了与血红蛋白相关的途径的显著丰富,包括铁代谢,氧化应激和炎症.
- 一个共同表达网络绘制了关键的lncRNAs和mRNAs之间的相互作用,这些相互作用与铁失调和慢性炎症有关.
结论:
- 在DFU中发现了与血红蛋白缺乏相关的明显的lncRNA-mRNA联合表达网络.
- 关键的lncRNA与参与铁处理和炎症的mRNA有很强的相关性,这表明它们对DFU病理的贡献.
- 这些发现突出了lncRNAs在贫血的DFU中的潜在调节作用,并为诊断开发提供了途径.
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