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Suv39h1 promotes facet joint chondrocyte proliferation by targeting miR-15a/Bcl2 in idiopathic scoliosis patients

机译:Suv39h1通过靶向miR-15a / Bcl2促进特发性脊柱侧弯患者的小关节软骨细胞增殖

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摘要

BackgroundIdiopathic scoliosis (IS) is a complex disease with an unclear etiology, and the worldwide prevalence is approximately 2–3%. As an important link between environmental factors and phenotypic differences, epigenetic changes, such as lncRNA, miRNA, and DNA methylation, have recently been reported to be associated with the development of IS. However, the correlation between histone methylation, another classical epigenetic mechanism, and IS has not been determined. In this study, we investigated the morphological changes, alterations in the levels of histone methylation, and cell proliferation-related pathway in inferior facet joint cartilage in 11 IS patients and 10 comparable controls.
机译:背景特发性脊柱侧凸(IS)是一种病因不明的复杂疾病,全世界的患病率约为2-3%。作为环境因素与表型差异之间的重要联系,最近有报道称表观遗传学变化(如lncRNA,miRNA和DNA甲基化)与IS的发展有关。但是,还没有确定组蛋白甲基化(另一种经典的表观遗传机制)与IS之间的相关性。在这项研究中,我们调查了11名IS患者和10名可比较对照组的下小关节软骨的形态变化,组蛋白甲基化水平的变化以及细胞增殖相关的途径。

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