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胃癌中DNA甲基化对miR-200c 141表达影响的研究
引用本文:周欣亮,张璁,王玉栋,赵连梅,桑梅香,单保恩.胃癌中DNA甲基化对miR-200c 141表达影响的研究[J].中国肿瘤临床,2017,44(2):73-77.
作者姓名:周欣亮  张璁  王玉栋  赵连梅  桑梅香  单保恩
作者单位:①.河北医科大学第四医院肿瘤内科(石家庄市 050011)
摘    要:  目的  探讨胃癌组织中miR-200c/141CpG岛的甲基化水平与miR-200c/141表达水平和临床病理特征的相关性。  方法  运用实时定量PCR(qRT-PCR)和BS-MSP方法检测胃癌组织和癌旁组织中miR-200c/141CpG岛的表达与其基因甲基化水平。统计学分析miR-200c/141CpG岛的甲基化水平与miR-200c/141水平和临床病理特征的关系。  结果  miR-200c/141CpG岛的甲基化水平在胃癌组织中显著升高,miR-200c和miR-141的水平显著降低,miR-200c/141CpG岛的甲基化水平与miR-200c和miR-141的水平呈负相关。  结论  胃癌组织中升高的miR-200c/141CpG岛的甲基化水平诱导miR-200c和miR-141表达降低。 

关 键 词:胃癌    甲基化    miR-200c    miR-141    临床病理特征
收稿时间:2016-09-23

MiR-200c/141 methylation inhibits the expression of miR-200c and miR-141 in gastric cancer
Xinliang ZHOU,Cong ZHANG,Yudong WANG,Lianmei ZHAO,Meixiang SANG,Baoen SHAN.MiR-200c/141 methylation inhibits the expression of miR-200c and miR-141 in gastric cancer[J].Chinese Journal of Clinical Oncology,2017,44(2):73-77.
Authors:Xinliang ZHOU  Cong ZHANG  Yudong WANG  Lianmei ZHAO  Meixiang SANG  Baoen SHAN
Institution:①.Oncology Department, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China②.Research Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China③.Tumor Research Institute of Hebei, Shijiazhuang 050011, China
Abstract:Objective:This work aims to detect the levels of miR-200c/141 methylation and miR-200c/141 in gastric cancer tissue and investigate the relationship between miR-200c/141 expression and clinical parameters. Methods:The methylation status of miR-200c/141 CpG island and miR-200c/141 in gastric cancer tissue specimens was evaluated by qRT-PCR or BS-MSP method. We analyzed the relationship among the methylation status of miR-200c/141 CpG island, expression level of miR-200c or miR-141, and clinical parame-ters. Results:The status of miR-200c/141 CpG island methylation in gastric cancer tissue was significantly higher compared with that in paracarcinoma tissue. MiR-200c and miR-141 were markedly decreased in gastric cancer tissue compared with those in adjacent tis-sue. MiR-200c/141 CpG island methylation was negatively related with the expression of miR-200c and miR-141 in gastric cancer speci-mens. Conclusion:The upregulation of miR-200c/141 CpG methylation inhibits miR-200c/141 expression in gastric cancer tissue.
Keywords:gastric cancer  methylation  miR-200c  miR-141  clinicopathological feature
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