运行x2
成骨细胞
转录因子
Wnt信号通路
细胞生物学
小RNA
细胞分化
生物
骨重建
内分泌学
信号转导
遗传学
基因
体外
作者
Akshaya Muthuswamy Narayanan,N. Srinaath,M. Rohini,N. Selvamurugan
出处
期刊:Life Sciences
[Elsevier BV]
日期:2019-07-21
卷期号:232: 116676-116676
被引量:104
标识
DOI:10.1016/j.lfs.2019.116676
摘要
Bone is one of the most dynamic organs in the body that continuously undergoes remodeling through bone formation and resorption. A cascade of molecules and pathways results in the osteoblast differentiation that is attributed to osteogenesis, or bone formation. The process of osteogenesis is achieved through participation of the Wnt pathway, FGFs, BMPs/TGF-β, and transcription factors such as Runx2 and Osx. The activity and function of the master transcription factor, Runx2, is of utmost significance as it can induce the function of osteoblast differentiation markers. A number of microRNAs [miRNAs] have been recently identified in the regulation of Runx2 expression/activity, thus affecting the process of osteogenesis. miRNAs that target Runx2 corepressors favor osteogenesis, while miRNAs that target Runx2 coactivators inhibit osteogenesis. In this review, we focus on the regulation of Runx2 by miRNAs in osteoblast differentiation and their potential for treating bone and bone-related diseases.
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