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软骨衰老中的微小RNA分析

MicroRNA Profiling in Cartilage Ageing.

作者信息

Balaskas Panagiotis, Goljanek-Whysall Katarzyna, Clegg Peter, Fang Yongxiang, Cremers Andy, Emans Pieter, Welting Tim, Peffers Mandy

机构信息

Institute of Ageing and Chronic Disease, William Henry Duncan Building, 6 West Derby Street, Liverpool L7 8TX, UK.

Centre for Genomic Research, Institute of Integrative Biology, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, UK.

出版信息

Int J Genomics. 2017;2017:2713725. doi: 10.1155/2017/2713725. Epub 2017 Aug 14.

Abstract

Osteoarthritis (OA) is the most common age-related joint disorder in man. MicroRNAs (miRNA), a class of small noncoding RNAs, are potential therapeutic targets for regulating molecular mechanisms in both disease and ageing. Whilst there is an increasing amount of research on the roles of miRNAs in ageing, there has been scant research on age-related changes in miRNA in a cartilage. We undertook a microarray study on young and old human cartilages. Findings were validated in an independent cohort. Contrasts between these samples identified twenty differentially expressed miRNAs in a cartilage from old donors, derived from an OA environment which clustered based on OA severity. We identified a number of recognised and novel miRNAs changing in cartilage ageing and OA including miR-126: a potential new candidate with a role in OA pathogenesis. These analyses represent important candidates that have the potential as cartilage ageing and OA biomarkers and therapeutic targets.

摘要

骨关节炎(OA)是人类最常见的与年龄相关的关节疾病。微小RNA(miRNA)是一类小的非编码RNA,是调节疾病和衰老分子机制的潜在治疗靶点。虽然关于miRNA在衰老中的作用的研究越来越多,但关于软骨中miRNA与年龄相关变化的研究却很少。我们对年轻和年老的人类软骨进行了微阵列研究。研究结果在一个独立队列中得到验证。这些样本之间的对比确定了来自老年供体软骨中的20种差异表达的miRNA,这些miRNA来自基于OA严重程度聚类的OA环境。我们鉴定出了一些在软骨衰老和OA中发生变化的已知和新型miRNA,包括miR-126:一种在OA发病机制中起作用的潜在新候选物。这些分析代表了具有作为软骨衰老和OA生物标志物及治疗靶点潜力的重要候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c615/5584353/743a0e505a8e/IJG2017-2713725.001.jpg

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