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RNA 测序鉴定全髋关节置换术后和骨关节炎中的溶骨关键基因和长链非编码 RNA。

Identification of Critical Genes and lncRNAs in Osteolysis after Total Hip Arthroplasty and Osteoarthritis by RNA Sequencing.

机构信息

Department of Joint Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250000, China.

Department of Orthopaedics, Shandong Provincial Hospital (Group) Ludong Hospital, Yantai 264000, China.

出版信息

Biomed Res Int. 2021 Mar 13;2021:6681925. doi: 10.1155/2021/6681925. eCollection 2021.

Abstract

Total hip arthroplasty (THA) is a cost-effective treatment for osteoarthritis (OA), and osteolysis is a common complication of THA. This study was aimed at exploring the relevant molecular biomarkers for osteolysis after THA. We performed RNA sequence to identify and characterize expressed mRNAs and lncRNAs in OA and osteolysis. Differentially expressed mRNAs (DEmRNAs) and lncRNAs (DElncRNAs) in OA and osteolysis were acquired, as well as shared DEmRNAs/DElncRNAs in OA and osteolysis and osteolysis-specific DEmRNAs/DElncRNAs. Then, shared and osteolysis-specific DElncRNA-DEmRNA coexpression networks were constructed to further investigate the function of DElncRNAs and DEmRNAs in OA and osteolysis. In total, 343 DEmRNAs and 25 DElncRNAs in OA, 908 DEmRNAs and 107 DElncRNAs in osteolysis, and 406 DEmRNAs and 46 DElncRNAs between OA and osteolysis were acquired. A total of 136 shared DEmRNAs and 9 shared DElncRNAs in OA and osteolysis and 736 osteolysis-specific DEmRNAs and 103 osteolysis-specific DElncRNAs were acquired. Then, 128 shared DElncRNA-DEmRNA coexpression pairs and 522 osteolysis-specific DElncRNA-DEmRNA coexpression pairs were identified. The present study highlighted the roles of four interaction pairs, including two shared lncRNA-mRNA interaction pairs in OA and osteolysis (AC111000.4 and AC016831.6), which may function in the immune process of OA and osteolysis by regulating CD8A and CD8B, respectively, and two osteolysis-specific interaction pairs (AC090607.4-FOXO3 and TAL1-ABALON), which may play an important role in osteoclastogenesis.

摘要

全髋关节置换术 (THA) 是治疗骨关节炎 (OA) 的一种具有成本效益的方法,而溶骨是 THA 的常见并发症。本研究旨在探讨 THA 后溶骨的相关分子生物标志物。我们进行了 RNA 测序,以鉴定和描述 OA 和溶骨中表达的 mRNAs 和 lncRNAs。获得了 OA 和溶骨中的差异表达 mRNAs (DEmRNAs) 和 lncRNAs (DElncRNAs),以及 OA 和溶骨中共享的 DEmRNAs/DElncRNAs 和溶骨特异性 DEmRNAs/DElncRNAs。然后,构建了共享和溶骨特异性 DElncRNA-DEmRNA 共表达网络,以进一步研究 DElncRNAs 和 DEmRNAs 在 OA 和溶骨中的功能。总共获得了 OA 中的 343 个 DEmRNAs 和 25 个 DElncRNAs,溶骨中的 908 个 DEmRNAs 和 107 个 DElncRNAs,以及 OA 和溶骨之间的 406 个 DEmRNAs 和 46 个 DElncRNAs。获得了 OA 和溶骨中共有 136 个 DEmRNAs 和 9 个共有 DElncRNAs,以及 736 个溶骨特异性 DEmRNAs 和 103 个溶骨特异性 DElncRNAs。然后,鉴定了 128 个共享 DElncRNA-DEmRNA 共表达对和 522 个溶骨特异性 DElncRNA-DEmRNA 共表达对。本研究强调了四个相互作用对的作用,包括 OA 和溶骨中两个共有 lncRNA-mRNA 相互作用对(AC111000.4 和 AC016831.6),它们分别通过调节 CD8A 和 CD8B 可能在 OA 和溶骨的免疫过程中发挥作用,以及两个溶骨特异性相互作用对(AC090607.4-FOXO3 和 TAL1-ABALON),它们可能在破骨细胞发生中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc59/7984875/4a11359b0146/BMRI2021-6681925.001.jpg

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