Whole-transcriptome sequencing and ceRNA interaction network of temporomandibular joint osteoarthritis.
Whole-transcriptome sequencing and ceRNA interaction network of temporomandibular joint osteoarthritis.
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颞下颌关节骨关节炎的全转录组测序和ceRNA相互作用网络
DOI:
10.3389/fgene.2022.962574
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发表时间:
2022
影响因子:
3.7
通讯作者:
Wu, Gaoyi
中科院分区:
文献类型:
--
作者:
Wu, Fan;An, Yanxin;Zhou, Libo;Zhao, Yuqing;Chen, Lei;Wang, Jing;Wu, Gaoyi
关键词:
Purpose: The aim of this study was to conduct a comprehensive transcriptomic analysis to explore the potential biological functions of noncoding RNA (ncRNAs) in temporomandibular joint osteoarthritis (TMJOA). Methods: Whole transcriptome sequencing was performed to identify differentially expressed genes (DEGs) profiles between the TMJOA and normal groups. The functions and pathways of the DEGs were analyzed using Metascape, and a competitive endogenous RNA (ceRNA) network was constructed using Cytoscape software. Results: A total of 137 DEmRNAs, 65 DEmiRNAs, 132 DElncRNAs, and 29 DEcircRNAs were identified between the TMJOA and normal groups. Functional annotation of the DEmRNAs revealed that immune response and apoptosis are closely related to TMJOA and also suggested key signaling pathways related to TMJOA, including chronic depression and PPAR signaling pathways. We identified vital mRNAs, including Klrk1, Adipoq, Cryab, and Hspa1b. Notably, Adipoq expression in cartilage was significantly upregulated in TMJOA compared with normal groups (10-fold, p < 0.001). According to the functional analysis of DEmRNAs regulated by the ceRNA network, we found that ncRNAs are involved in the regulation of autophagy and apoptosis. In addition, significantly DEncRNAs (lncRNA-COX7A1, lncRNA-CHTOP, lncRNA-UFM1, ciRNA166 and circRNA1531) were verified, and among these, circRNA1531 (14.5-fold, p < 0.001) and lncRNA-CHTOP (14.8-fold, p < 0.001) were the most significantly downregulated ncRNAs. Conclusion: This study showed the potential of lncRNAs, circRNAs, miRNAs, and mRNAs may as clinical biomarkers and provides transcriptomic insights into their functional roles in TMJOA. This study identified the transcriptomic signatures of mRNAs associated with immunity and apoptosis and the signatures of ncRNAs associated with autophagy and apoptosis and provides insight into ncRNAs in TMJOA.
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影响因子:
3.4
作者:
He P;Zhang Z;Liao W;Xu D;Fu M;Kang Y
通讯作者:
Kang Y
DOI:
10.1016/j.clim.2012.12.011
发表时间:
2013-03
期刊:
Clinical immunology (Orlando, Fla.)
影响因子:
--
作者:
Haseeb A;Haqqi TM
通讯作者:
Haqqi TM
影响因子:
12.3
作者:
Marchese FP;Raimondi I;Huarte M
通讯作者:
Huarte M
影响因子:
5.6
作者:
Musumeci G;Castrogiovanni P;Trovato FM;Weinberg AM;Al-Wasiyah MK;Alqahtani MH;Mobasheri A
通讯作者:
Mobasheri A
DOI:
10.1111/febs.12005
发表时间:
2012-11
期刊:
The FEBS journal
影响因子:
--
作者:
Oh DH;Rigas D;Cho A;Chan JY
通讯作者:
Chan JY