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[非编码RNA调控骨关节炎的分子生物学研究进展]

[Molecular biological research progress of non-coding RNAs modulating osteoarthritis].

作者信息

Jia Di, Li Yanlin, Wang Kun, Cai Guofeng, Yang Lingjian, Meng Xuhan

机构信息

Department of Sports Medicine, First Affiliated Hospital of Kunming Medical University, Kunming Yunnan, 650000, P.R.China.

Department of Sports Medicine, First Affiliated Hospital of Kunming Medical University, Kunming Yunnan, 650000,

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Mar 15;31(3):374-378. doi: 10.7507/1002-1892.201610123.

Abstract

OBJECTIVE

To summarize the molecular biological research progress of non-coding RNAs modulating osteoarthritis (OA), and provide a reference basis for biological study and clinical treatment of OA.

METHODS

Recent domestic and foreign related literature about the regulation of OA pathological process by non-coding RNAs was widely reviewed.

RESULTS

Non-coding RNAs can be divided into three types based on the length of RNA. A lot of non-coding RNAs participating in OA pathological process are screened out by high throughput sequencing technology and microarray technology, and it is verified that these non-coding RNAs involve in the regulation of OA by RT-PCR. The mechanism of OA mediated target is clarified by knocking-down and overexpressing of the most prominent expressed non-coding RNAs in OA. There are the complicated gene expressed network topology in non-coding RNAs, and between non-coding RNAs and coding RNAs. It provides a basis for clearing the effect of gene structure and function, and finding the definite therapeutic target of OA.

CONCLUSION

There is preliminary study on molecular biological mechanism of non-coding RNAs mediating OA, but the key structure or sequence of non-coding RNAs, formation and interaction of effecting composite structure about mediating OA are unknown, and it needs further study.

摘要

目的

总结非编码RNA调控骨关节炎(OA)的分子生物学研究进展,为OA的生物学研究及临床治疗提供参考依据。

方法

广泛查阅国内外近期关于非编码RNA调控OA病理过程的相关文献。

结果

非编码RNA根据RNA长度可分为三类。通过高通量测序技术和基因芯片技术筛选出许多参与OA病理过程的非编码RNA,并通过逆转录聚合酶链反应(RT-PCR)验证这些非编码RNA参与OA的调控。通过敲低和过表达OA中表达最突出的非编码RNA来阐明OA介导靶点的机制。非编码RNA之间以及非编码RNA与编码RNA之间存在复杂的基因表达网络拓扑结构。这为明确基因结构和功能的作用以及寻找OA确切的治疗靶点提供了依据。

结论

关于非编码RNA介导OA的分子生物学机制已有初步研究,但非编码RNA的关键结构或序列、介导OA的效应复合结构的形成及相互作用尚不清楚,有待进一步研究。

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