Zhou Hailun, Xiang Rong, Chen Wenjin, Peng Yuanyuan, Chen Zhiyong, Chen Wenxia, Tang Li
Guangxi Medical University, Nanning, 530021, China.
Guangxi Key Laboratory of the Rehabilitation and Reconstruction of Oral and Maxillofacial Research, Nanning, 530021, China.
Eur J Med Res. 2024 Dec 19;29(1):594. doi: 10.1186/s40001-024-02153-3.
Performing a comprehensive study on the differential expression of mRNAs, miRNAs, and circRNAs in the context of peri-implantitis and periodontitis has beneficial advantages to identify unique molecular signatures and pathways that may contribute to our understanding of these conditions.
Gingival tissues from healthy individuals and peri-implantitis and periodontitis patients were obtained to identify differential expression genes (DEG) by Illumina HiSeq 2500 instrument. Differential expression analysis was conducted using R statistical software, with significance set at P < 0.05 and fold greater than 2. Functional enrichment analysis of the DEGs was conducted using the Reactome, Gene ontology and KEGG databases.
Significant differences in mRNA, miRNA, and circRNA profiles were identified between healthy gingival tissues. The top DEGs comprising 6 circRNAs, 2 miRNAs, and 4 mRNAs were identified and the constructed ceRNA network, elucidates their involvement in key signaling pathways such as ErbB, Wnt, and mTOR, which are crucial for understanding the inflammatory progression of these conditions.
This study highlights a heterogeneous circRNA-mediated ceRNA regulatory mechanism in peri-implantitis and periodontitis, activating signaling pathways and regulating gene expression. Key findings including a detailed analysis of the transcriptional landscape and identification of unique molecular signatures, pathways and cellular components in gingival tissues, offering insights into the molecular differences between peri-implantitis and periodontitis. The study may contribute to the understanding of the pathological mechanisms of these diseases and may aid in the development of targeted therapies.
在种植体周围炎和牙周炎背景下对mRNA、miRNA和circRNA的差异表达进行全面研究,对于识别可能有助于我们理解这些病症的独特分子特征和途径具有有益优势。
获取健康个体以及种植体周围炎和牙周炎患者的牙龈组织,通过Illumina HiSeq 2500仪器鉴定差异表达基因(DEG)。使用R统计软件进行差异表达分析,显著性设定为P < 0.05且倍数大于2。使用Reactome、基因本体论和KEGG数据库对DEG进行功能富集分析。
在健康牙龈组织之间鉴定出mRNA、miRNA和circRNA谱的显著差异。鉴定出由6种circRNA、2种miRNA和4种mRNA组成的顶级DEG,并构建了ceRNA网络,阐明了它们参与如ErbB、Wnt和mTOR等关键信号通路,这些通路对于理解这些病症的炎症进展至关重要。
本研究突出了种植体周围炎和牙周炎中由circRNA介导的异质性ceRNA调控机制,激活信号通路并调节基因表达。主要发现包括对转录图谱的详细分析以及牙龈组织中独特分子特征、途径和细胞成分的鉴定,为种植体周围炎和牙周炎之间的分子差异提供了见解。该研究可能有助于理解这些疾病的病理机制,并可能有助于开发靶向治疗方法。