Chen Jindong, Zhang Shilong, Cai Dixin, Yin Qing, Xie Qian, Xu Pengfang, Zhu Junling
Department of Orthopedics, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Qingyuan, 511518, China.
Department of Orthopedics and Traumatology, Shanghai Fengxian District Hospital of Traditional Chinese Medicine, Shanghai, 201499, China.
Hereditas. 2025 Jul 10;162(1):124. doi: 10.1186/s41065-025-00494-5.
Numerous long noncoding RNAs (lncRNAs) have been proven to participate in osteogenesis and postmenopausal osteoporosis (PMOP). We measured serum SDCBP2-AS1 expression changes in patients with PMOP and investigated its effects on osteoblast differentiation in human bone marrow-derived mesenchymal stem cells (hBMSC) cells.
RT-qPCR was used to measure SDCBP2-AS1 levels and the expression of osteogenic differentiation indicators. The diagnostic efficacy of SDCBP2-AS1 was assessed using a receiver operating characteristic (ROC) analysis. CCK-8 and flow cytometry methods were employed to investigate the functional impact of SDCBP2-AS1 on hBMSC cell proliferation and apoptosis during osteoblast differentiation. The bioinformatics, dual-luciferase reporter assay, and RNA Immunoprecipitation (RIP) assay were used to identify and confirm SDCBP2-AS1/miR-361-3p interaction.
Serum SDCBP2-AS1 was decreased in patients with PMOP, especially in those with fractures. The SDCBP2-AS1 levels were positively correlated with patients' T scores and BMDs. Decreased SDCBP2-AS1 had a certain high area under the ROC curve (AUC) value (AUC = 0.81) in distinguishing PMOP patients with fractures from those without fractures. SDCBP2-AS1 levels gradually increased after four weeks of treatment in PMOP patients and hBMSCs during cell differentiation. Enhanced SDCBP2-AS1 promoted cell proliferation and the levels of osteoblast differentiation markers, including ALP, OCN, RUNX2, and Collagen I, while decreasing cell apoptosis. miR-361-3p was a direct target of SDCBP2-AS1. The influence of SDCBP2-AS1 on cell activities and hBMSCs differentiation was diminished by miR-361-3p.
SDCBP2-AS1 might be a diagnostic biomarker in predicting PMOP patients with fractures. By measuring the levels of SDCBP2-AS1 in patient samples, clinicians may be able to identify those who are more susceptible to bone fractures, enabling earlier and more targeted preventive measures. SDCBP2-AS1 targeting miR-361-3p regulates the osteogenic differentiation of hBMSCs, which might be a new target for the treatment of PMOP.
大量长链非编码RNA(lncRNAs)已被证明参与骨生成和绝经后骨质疏松症(PMOP)。我们检测了PMOP患者血清中SDCBP2-AS1的表达变化,并研究了其对人骨髓间充质干细胞(hBMSC)成骨细胞分化的影响。
采用RT-qPCR检测SDCBP2-AS1水平和成骨分化指标的表达。使用受试者工作特征(ROC)分析评估SDCBP2-AS1的诊断效能。采用CCK-8和流式细胞术方法研究SDCBP2-AS1对成骨细胞分化过程中hBMSC细胞增殖和凋亡的功能影响。运用生物信息学、双荧光素酶报告基因检测和RNA免疫沉淀(RIP)检测来鉴定和确认SDCBP2-AS1/miR-361-3p相互作用。
PMOP患者血清中SDCBP2-AS1降低,尤其是骨折患者。SDCBP2-AS1水平与患者的T值和骨密度呈正相关。在区分有骨折和无骨折的PMOP患者方面,SDCBP2-AS1水平降低具有一定的曲线下面积(AUC)值(AUC = 0.81)。在PMOP患者和细胞分化过程中的hBMSC中,治疗四周后SDCBP2-AS1水平逐渐升高。增强的SDCBP2-AS1促进细胞增殖和成骨分化标志物的水平,包括碱性磷酸酶(ALP)、骨钙素(OCN)、RUNX2和I型胶原蛋白,同时减少细胞凋亡。miR-361-3p是SDCBP2-AS1的直接靶点。miR-361-3p减弱了SDCBP2-AS1对细胞活性和hBMSC分化的影响。
SDCBP2-AS1可能是预测有骨折的PMOP患者的诊断生物标志物。通过检测患者样本中SDCBP2-AS1的水平,临床医生或许能够识别出那些更易发生骨折的患者,从而采取更早且更具针对性的预防措施。SDCBP2-AS1靶向miR-361-3p调节hBMSC的成骨分化,这可能是治疗PMOP的新靶点。