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冠状动脉支架内再狭窄相关miRNA的表达谱分析和意义

魏广和 蔺跃栋 苏强 刘立新 张韶辉 杨国良 郭莹 张淑芳

中国动脉硬化杂志2017,Vol.25Issue(8):800-806,7.
中国动脉硬化杂志2017,Vol.25Issue(8):800-806,7.

冠状动脉支架内再狭窄相关miRNA的表达谱分析和意义

MicroRNA profiling and significance in coronary in-stent restenosis

魏广和 1蔺跃栋 2苏强 1刘立新 2张韶辉 3杨国良 1郭莹 2张淑芳1

作者信息

  • 1. 济宁医学院附属医院心内科,山东省济宁市272029
  • 2. 济宁医学院附属医院山东省心脏疾病诊疗重点实验室,山东省济宁市272029
  • 3. 济宁医学院附属医院健康管理中心,山东省济宁市272029
  • 折叠

摘要

Abstract

Aim To screen out the specific expression of miRNA in ISR,and its significance was analyzed by bioinformatics method.Methods The expression profiles of miRNA in ISR patients were screened by miRNA gene chip to screen out ISR related miRNA.The relative expression of miRNA and ISR was verfied by Real-time PCR.miRNA target genes were predicted by bioinformatics,and data mining of the downstream target genes of miRNA was carried out,and the ISR related miRNA-Gene-Network was constructed,the possible mechanism of ISR was discussed.Results The difference expression of miRNA in ISR patients was detected by high throughput miRNA microarray,43 genes were down regulated and 10 genes were up-regulated.Bioinformatics and Real-time PCR were used to verfy the result of microarray.A number of miRNA and target genes related to ISR were obtained,and the regulatory networks of miRNA and target genes were constructed miRNA-Gene-Network.Quantitative detection of Real-time PCR quantitative detection showed that miR-126 in group ISR was significantly lower than that in group non-ISR (0.507±0.131 vs.1.427±0.337,P<0.05).Conclusion The expression of miRNA in ISR patients is different from no-ISR,these miRNA and target genes may be related to the occurrence of ISR,the decrease of miR-126 level tended to occur in ISR.

关键词

冠心痛/支架内再狭窄/miRNA/生物信息学

Key words

Coronary artery disease/In-stent restenosis/miRNA/Bioinformatics

分类

医药卫生

引用本文复制引用

魏广和,蔺跃栋,苏强,刘立新,张韶辉,杨国良,郭莹,张淑芳..冠状动脉支架内再狭窄相关miRNA的表达谱分析和意义[J].中国动脉硬化杂志,2017,25(8):800-806,7.

基金项目

山东省医药卫生科技发展项目(2014WS0515) (2014WS0515)

济宁医学院重点项目(JY2013KJ005) (JY2013KJ005)

中国动脉硬化杂志

OACSTPCD

1007-3949

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