变应性鼻炎继发哮喘患者血浆microRNA表达谱的改变
作者:
作者简介:

胡陟, Email:jhcw001@163.com

基金项目:

江苏省自然科学基金(BK20161388)


Changes of plasma microRNAs expression profiles in allergic rhinitis patients with secondary asthma
  • 摘要
  • | |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
    摘要:

    目的应用microRNA表达谱芯片技术,选取临床明确诊断的变应性鼻炎(allergic rhinitis, AR)及变应性鼻炎罹患哮喘(asthma, AS)患者相应血浆,分析变应性鼻炎患者罹患哮喘后血浆microRNA的差异性表达。方法选取AR及AR+AS各3例,使用miRCURY LNATM芯片,筛选出两组患者血浆中差异表达的microRNA并进行聚类分析;最后通过生物信息学分析预测其靶基因。结果与AR组相比较,AR+AS组差异表达的microRNA共有9个,其中表达下调的有4个,表达上调的有5个。靶基因预测显示,以黏附连接、Wnt和MAPK信号传导通路靶基因的差异表达最为显著。结论通过microRNA芯片发现的相关差异性表达的microRNA,有可能成为AR患者罹患AS的易感性生物标志物及临床可能的治疗靶点,但是尚需要进一步靶基因验证及功能学分析。

    Abstract:

    ObjectiveTo detect the differential expressions of plasma microRNAs in allergic rhinitis (AR) patients with secondary asthma (AS) via microRNA expression profile chip technology.MethodsPlasma samples were collected from patients suffering from AR (AR group)and AR patients with secondary AS (AR+AS group) respectively, and each group had 3 cases. The plasma microRNAs differentially expressed in AR+AS group were screened out by miRCURY LNATM chip and analyzed with cluster analysis. Finally, target genes were predicted by biological informatics technology.ResultsCompared with AR group, 9 microRNAs were differentially expressed in AR+AS group. Of them, the expression was upregulated in 4 and downregulated in 5. Target gene prediction showed that target genes of adherens junction, Wnt and mitogenactivated protein kinase (MAPK) signaling pathways were differentially expressed most predominately.ConclusionThe differentially expressed plasma microRNAs screened out by microRNA chip technology may be biomarkers of susceptibility in AR patients to AS and therapeutic targets for this disease.

    参考文献
    相似文献
    引证文献
引用本文

吴昆旻,李泽卿,马莉,陈伟,安静娟,沈洁,杨祁,朱春晖,胡陟.变应性鼻炎继发哮喘患者血浆microRNA表达谱的改变[J].中国耳鼻咽喉颅底外科杂志,2017,23(1):16-19

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
历史
  • 在线发布日期: 2017-02-28
温馨提示

本刊唯一投稿网址:www.xyosbs.com
唯一办公邮箱:xyent@126.com
编辑部联系电话:0731-84327210,84327469
本刊从未委托任何单位、个人及其他网站代理征稿及办理其他业务联系,谨防上当受骗!

关闭