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作 者:王鑫[1] 王姗[1] 孟琰[1] 强冬霞 施磊[1] 苏艳国 赵尔杨[1]
机构地区:[1]哈尔滨医科大学第一临床医学院.口腔医学院口腔病理科,黑龙江哈尔滨150001
出 处:《口腔医学研究》2016年第5期470-473,共4页Journal of Oral Science Research
基 金:全国"重生行动"李嘉诚科研基金项目(无项目编号)
摘 要:目的:探讨非综合征性唇腭裂患者中microRNA表达谱差异及显著改变microRNA与WNT家族的关联性。方法:采用涵盖当前miRbase数据库中所有人类microRNA的miRCURY^(TM)探针的基因芯片对4例非综合征性唇腭裂患者的唇腭组织与4例正常新生儿脐带组织所提取的microRNA进行分析研究,并对差异性表达显著的microRNA进行生物信息学分析。结果:共筛选出254个与非综合征性唇腭裂相关的差异表达microRNA:181个在非综合征性唇腭裂组织中表达上调,73个表达下调(P<0.05)。根据差异倍数与P值大小,选取十个表达差异较大的microRNAs进行生物信息学靶基因预测,结果显示hsa-miR-1260b,hsa-miR-205-5p,hsa-miR-24-3p,hsa-miR-27b-3p和hsa-miR-720均靶向结合于Wnt5a、Wnt9b、Wnt10a等Wnt家族的信号分子。结论:差异表达较显著的microRNA通过与Wnt家族信号分子靶向结合参与调控唇腭裂的发育过程。Objective:To investigate the miRNA expression in nonsyndromic cleft lip patients with or without cleft palate and its correlation with Wnt family in nonsyndromic cleft lip patients with or without cleft palate.Methods:Gene chips of MiRCURYTM probe were used to detect and compare the microRNA expression of the lip and palate tissues in 4NSCL/P patients as well as umbilical cord tissues in 4normal newborns.Results:In total,254 differentially expressed miRNAs were detected,among which 181up-regulate and 73down-regulate(P〈0.05).According to the fold change and P value,the top ten different miRNAs were selected for target prediction.The results showed that hsa-miR-1260 b,hsa-miR-205-5p,hsa-miR-24-3p,hsa-miR-27b-3p and hsamiR-720 are combined with Wnt5 a,Wnt9band Wnt10 a.Conclusion:Differentially expressed miRNA may control the development of lip and palate by targeting Wnt family in embryonic period.
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