Suppr超能文献

青少年特发性脊柱侧凸中长链非编码RNA的表达特征

Expression Signatures of Long Noncoding RNAs in Adolescent Idiopathic Scoliosis.

作者信息

Liu Xiao-Yang, Wang Liang, Yu Bin, Zhuang Qian-Yu, Wang Yi-Peng

机构信息

Department of Orthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Shuaifuyuan, Wangfujing, Dongcheng District, Beijing 100730, China ; Department of Spine Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong 250000, China.

Department of Orthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Shuaifuyuan, Wangfujing, Dongcheng District, Beijing 100730, China.

出版信息

Biomed Res Int. 2015;2015:276049. doi: 10.1155/2015/276049. Epub 2015 Sep 1.

Abstract

PURPOSE

Adolescent idiopathic scoliosis (AIS), the most common pediatric spinal deformity, is considered a complex genetic disease. Causing genes and pathogenesis of AIS are still unclear. This study was designed to identify differentially expressed long noncoding RNAs (lncRNAs) involving the pathogenesis of AIS.

METHODS

We first performed comprehensive screening of lncRNA and mRNA in AIS patients and healthy children using Agilent human lncRNA + mRNA Array V3.0 microarray. LncRNAs expression in different AIS patients was further evaluated using quantitative PCR.

RESULTS

A total of 139 lncRNAs and 546 mRNAs were differentially expressed between AIS patients and healthy control. GO and Pathway analysis showed that these mRNAs might be involved in bone mineralization, neuromuscular junction, skeletal system morphogenesis, nucleotide and nucleic acid metabolism, and regulation of signal pathway. Four lncRNAs (ENST00000440778.1, ENST00000602322.1, ENST00000414894.1, and TCONS_00028768) were differentially expressed between different patients when grouped according to age, height, classification, severity of scoliosis, and Risser grade.

CONCLUSIONS

This study demonstrates the abnormal expression of lncRNAs and mRNAs in AIS, and the expression of some lncRNAs was related to clinical features. This study is helpful for further understanding of lncRNAs in pathogenesis, treatment, and prognosis of AIS.

摘要

目的

青少年特发性脊柱侧凸(AIS)是最常见的儿童脊柱畸形,被认为是一种复杂的遗传性疾病。AIS的致病基因和发病机制仍不清楚。本研究旨在鉴定与AIS发病机制相关的差异表达长链非编码RNA(lncRNA)。

方法

我们首先使用安捷伦人类lncRNA + mRNA Array V3.0芯片对AIS患者和健康儿童进行lncRNA和mRNA的全面筛选。使用定量PCR进一步评估不同AIS患者中lncRNA的表达。

结果

AIS患者与健康对照之间共有139个lncRNA和546个mRNA差异表达。基因本体(GO)和通路分析表明,这些mRNA可能参与骨矿化、神经肌肉接头、骨骼系统形态发生、核苷酸和核酸代谢以及信号通路调节。根据年龄、身高、分类、脊柱侧凸严重程度和Risser分级分组时,不同患者之间有4个lncRNA(ENST00000440778.1、ENST00000602322.1、ENST00000414894.1和TCONS_00028768)差异表达。

结论

本研究证明了AIS中lncRNA和mRNA的异常表达,且一些lncRNA的表达与临床特征相关。本研究有助于进一步了解lncRNA在AIS发病机制、治疗和预后中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabc/4569756/356738103db0/BMRI2015-276049.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验