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先天性巨结肠长链非编码RNA差异表达谱研究

田姣 郝丽军 王娅 陈鹏德 张薇 林燕 王宝西 江逊

中国实用儿科杂志2017,Vol.32Issue(6):458-462,5.
中国实用儿科杂志2017,Vol.32Issue(6):458-462,5.DOI:10.19538/j.ek2017060614

先天性巨结肠长链非编码RNA差异表达谱研究

Expression profile of long non-coding RNA in Hirschsprung's disease

田姣 1郝丽军 1王娅 1陈鹏德 1张薇 1林燕 1王宝西 1江逊1

作者信息

  • 1. 第四军医大学唐都医院儿科,陕西西安710038
  • 折叠

摘要

Abstract

Objective To investigate the long non-coding RNAs (lncRNAs) expression profiles in the bowels of patients with Hirschsprung disease (HSCR),and to explore the role of dysregulated lncRNAs in the pathogenesis of HSCR.Methods Thirty pairs of tissue samples,including aganglionic segments and ganglionic segments,were obtained from patients with HSCR during operation.Then lncRNA microarrays were used to investigate the expression profiles in 3 pairs of specimens coupled as HSCR tissues compared with matched normal colon tissues.Candidate genes were selected from these differentially expressed lncRNAs based on artificial criterion (raw signal intensity≥ 100;fold change≥ 3) and then validated by quantitative real-time polymerase chain reaction (qRT-PCR) in 27 pairs of tissues.Results A total of 217 lncRNAs in aganglionic colon segment were found to be more than two fold greater than that in ganglionic segment tissues,including 13 up-regulated and 204 down-regulated (P< 0.05).The expression of two lncRNAs were significantly changed in aganglionic tissues compared with the ganglionic tissues after qRT-PCR validation (P < 0.05),whereas the change of other lncRNAs selected from artificial criterion were without statistical difference (P>0.05).Conclusion Abnormal expression of lncRNAs is found in HSCR aganglionic segments,suggesting that lncRNAs may be involved in the pathogenesis of HSCR.

关键词

Hirschsprung病/基因表达谱/长链非编码RNA/基因芯片

Key words

Hirschsprung's disease/gene expression profiling/lncRNA/microarray

分类

医药卫生

引用本文复制引用

田姣,郝丽军,王娅,陈鹏德,张薇,林燕,王宝西,江逊..先天性巨结肠长链非编码RNA差异表达谱研究[J].中国实用儿科杂志,2017,32(6):458-462,5.

基金项目

国家自然科学基金资助项目(81170331 ()

81370490) ()

中国实用儿科杂志

OA北大核心CSCDCSTPCD

1005-2224

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