生物
竞争性内源性RNA
椎间盘
Wnt信号通路
细胞生物学
小RNA
核心
信号转导
PI3K/AKT/mTOR通路
小桶
长非编码RNA
微阵列
计算生物学
核糖核酸
生物信息学
遗传学
基因表达
基因
解剖
转录组
作者
Yanjiao Wu,Sen Li,Jianlin Shen,Zhiyun Wang,Huan Liu
出处
期刊:Genomics
[Elsevier BV]
日期:2023-02-04
卷期号:115 (2): 110570-110570
被引量:6
标识
DOI:10.1016/j.ygeno.2023.110570
摘要
In the present study, we aimed to have a comprehensive understanding of nucleus pulposus related long noncoding RNA (lncRNA) and mRNA expression profiles in intervertebral disc degeneration (IDD). In total, 2418 mRNAs and 528 lncRNAs were found to be differentially expressed in the IDD group compared with the Control group. Combining microarray datasets and sequencing data, 5 overlapping DEMs and 7 overlapping DELs were identified. NF-κB signaling pathway, PI3K-Akt signaling pathway and Wnt/β-catenin signaling pathway were strongly linked with enriched GO terms and KEGG pathways. The ceRNA network suggested that lnc-TMEM44-AS1-hsa-miR-206-HDAC4 may be one crucial axis in IDD. PPI network analysis was constructed with 309 nodes and 129 edges. And the highest connectivity degrees were ALB, APOB and CCL2. This study suggested that specific lncRNAs and ceRNA axes may be crucial in the development of IDD. It provides a new perspective for delaying IDD process and enhancing intervertebral disc repair.
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