Dysregulation of circRNA-0076906 and circRNA-0134944 is Correlated with Susceptibility to Osteoporosis and Osteoporotic Fracture in Postmenopausal Females from the Chinese Han Population.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacogenomics & Personalized Medicine Pub Date : 2023-01-01 DOI:10.2147/PGPM.S394757
Weijie Yang, Wei Zhang, Fengqian Li, Ning Xu, Ping Sun
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Abstract

Introduction: Many circRNAs, such as circRNA-0076906 and circRNA-0134944, have been reported to participate in the pathogenesis of osteoporosis via sponging miRNAs in postmenopausal female patients. In this study, we aimed to study potential signaling pathways underlying the role of certain circRNAs, miRNAs and their target genes in the pathogenesis of osteoporotic fracture in postmenopausal females.

Methods: Quantitative real-time PCR was performed to analyze the expression of circRNAs, miRNAs and their targets genes. Luciferase assays were carried out to explore the regulatory relationship between circ_0076906/miR-548i/OGN and circ_0134944/miR-630/TLR4.

Results: Osteoporosis and fracture were positively correlated to the expression of circ_0134944, miR-548i and TLR4, but negatively correlated to the expression of circ_0076906, miR-630 and OGN in the peripheral blood and bone tissue samples of postmenopausal women. Luciferase activities of wild-type circ_0076906 and OGN were inhibited by miR-548i, and the luciferase activities of wild-type circ_0134944 and TLR4 were suppressed by miR-630 in MG-63 and U-2 OS cells. Inhibition of circ_0076906 expression in MG-63 and U-2 OS cells activated the expression of miR-548i and inhibited the expression of OGN. Moreover, the overexpression of circ_0134944 in MG-63 and U-2 OS cells suppressed the expression of miR-630 and enhanced the expression of TLR4.

Conclusion: This study implied that the dysregulation of circRNA-0076906 and circRNA-0134944 modulated their specific signaling and thus contributed to the severity of osteoporosis, increasing the risk of osteoporotic fracture.

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circRNA-0076906和circRNA-0134944基因异常与中国汉族绝经后女性骨质疏松和骨质疏松性骨折易感性相关
许多circrna,如circRNA-0076906和circRNA-0134944,已被报道通过海绵mirna参与绝经后女性患者骨质疏松的发病机制。在这项研究中,我们旨在研究某些circRNAs、miRNAs及其靶基因在绝经后女性骨质疏松性骨折发病机制中的潜在信号通路。方法:采用实时荧光定量PCR方法分析circrna、mirna及其靶基因的表达情况。通过荧光素酶测定来探索circ_0076906/miR-548i/OGN与circ_0134944/miR-630/TLR4之间的调控关系。结果:绝经后妇女外周血和骨组织样本中,骨质疏松和骨折与circ_0134944、miR-548i、TLR4的表达呈正相关,与circ_0076906、miR-630、OGN的表达呈负相关。在MG-63和U-2 OS细胞中,miR-548i抑制野生型circ_0076906和OGN的荧光素酶活性,miR-630抑制野生型circ_0134944和TLR4的荧光素酶活性。抑制MG-63和U-2 OS细胞中circ_0076906的表达可激活miR-548i的表达,抑制OGN的表达。此外,circ_0134944在MG-63和U-2 OS细胞中的过表达抑制了miR-630的表达,增强了TLR4的表达。结论:本研究提示circRNA-0076906和circRNA-0134944的异常调节了它们的特异性信号,从而导致了骨质疏松的严重程度,增加了骨质疏松性骨折的风险。
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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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