Department of Clinical Pharmacology, College of Pharmacy, Dalian Medical University, 9 West Section, Lvshun South Road, Lvshunkou District, Dalian, 116044, China.
Department of Orthopaedics, The First Affiliated Hospital, Dalian Medical University, No. 222, Zhongshan Road, Xigang District, Dalian, 116011, China.
Sci Rep. 2022 Jun 9;12(1):9549. doi: 10.1038/s41598-022-13791-0.
Osteoporosis (OP) is a common bone disease of old age resulting from the imbalance between bone resorption and bone formation. CircRNAs are a class of endogenous non-coding RNAs (ncRNAs) involved in gene regulation and may play important roles in the development of OP. Here, we aimed to discover the OP‑related circRNA-miRNA-mRNA (ceRNA) network and the potential mechanisms. Six microarray datasets were obtained from the GEO database and the OP‑related differentially expressed genes (DEGs), circRNAs (DECs), and miRNAs (DEMs) were screened out from these datasets. Then, combined with the prediction of the relationships between DEGs, DEMs, and DECs, a ceRNA network containing 7 target circRNAs, 5 target miRNAs, and 38 target genes was constructed. Then the RNA-seq verification by using total RNAs isolated from the femurs of normal and ovariectomized Wistar rats indicated that MFAP5, CAMK2A, and RGS4 in the ceRNA network were closely associated with osteoporosis. Function enrichment analysis indicated that the target circRNAs, miRNAs, and genes were involved in the process of MAPK cascade, hormone stimulus, cadherin binding, rRNA methyltransferase, PI3K-Akt signaling pathway, and Vitamin digestion and absorption, etc. Then a circRNA-miRNA-hub gene subnetwork was constructed and the qRT-PCR analysis of human bone tissues from the femoral head was used to confirm that the transcription of hsa_circR_0028877, hsa_circR_0082916, DIRAS2, CAMK2A, and MAPK4 showed a significant correlation with osteogenic genes. Besides, the two axes of hsa_circR_0028877/hsa-miR-1273f/CAMK2A and hsa_circR_0028877/hsa-miR-1273f/DIRAS2 conformed to be closely associated with OP. Additionally, by constructing a drug-target gene network, RKI-1447, FRAX486, Hyaluronic, and Fostamatinib were identified as therapeutic options for OP. Our study revealed the potential links between circRNAs, miRNAs, and mRNAs in OP, suggesting that the ceRNA mechanism might contribute to the occurrence of OP.
骨质疏松症(OP)是一种常见的老年骨骼疾病,源于骨吸收和骨形成之间的失衡。circRNAs 是一类参与基因调控的内源性非编码 RNA(ncRNAs),可能在 OP 的发展中发挥重要作用。在这里,我们旨在发现与 OP 相关的 circRNA-miRNA-mRNA(ceRNA)网络和潜在机制。从 GEO 数据库中获取了六个微阵列数据集,并从这些数据集中筛选出与 OP 相关的差异表达基因(DEGs)、circRNAs(DECs)和 microRNAs(DEMs)。然后,结合 DEGs、DEMs 和 DECs 之间关系的预测,构建了一个包含 7 个靶 circRNA、5 个靶 miRNA 和 38 个靶基因的 ceRNA 网络。然后,使用从正常和去卵巢 Wistar 大鼠股骨中分离的总 RNA 进行 RNA-seq 验证表明,ceRNA 网络中的 MFAP5、CAMK2A 和 RGS4 与骨质疏松症密切相关。功能富集分析表明,靶 circRNAs、miRNAs 和基因参与了 MAPK 级联、激素刺激、钙粘蛋白结合、rRNA 甲基转移酶、PI3K-Akt 信号通路和维生素消化吸收等过程。然后构建了一个 circRNA-miRNA-枢纽基因子网络,并使用人股骨头骨组织的 qRT-PCR 分析证实 hsa_circR_0028877、hsa_circR_0082916、DIRAS2、CAMK2A 和 MAPK4 的转录与成骨基因呈显著相关性。此外,hsa_circR_0028877/hsa-miR-1273f/CAMK2A 和 hsa_circR_0028877/hsa-miR-1273f/DIRAS2 这两个轴与 OP 密切相关。此外,通过构建药物-靶基因网络,鉴定出 RKI-1447、FRAX486、透明质酸和 fostamatinib 是治疗 OP 的选择。我们的研究揭示了 OP 中 circRNAs、miRNAs 和 mRNAs 之间的潜在联系,表明 ceRNA 机制可能有助于 OP 的发生。