miRNA―181a及其靶基因共济失调―毛细血管扩张突变基因在胃癌组织中表达及意义.docVIP

miRNA―181a及其靶基因共济失调―毛细血管扩张突变基因在胃癌组织中表达及意义.doc

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miRNA―181a及其靶基因共济失调―毛细血管扩张突变基因在胃癌组织中表达及意义

miRNA―181a及其靶基因共济失调―毛细血管扩张突变基因在胃癌组织中表达及意义   [摘要] 目的 观察胃癌组织中微小RNA-181a(miR-181a)与其靶基因共济失调-毛细血管扩张突变基因(ATM)的表达与异常情况,初步研究其意义。 方法 收集2009年4月~2011年12月广州市第一人民医院外科手术切除的胃癌组织标本9例,同时选取其癌旁非癌组织标本作为对照,分析胃癌组织中miR-181a与ATM蛋白表达的相关性。提取其蛋白质及总RNA,采用实时荧光定量PCR(qRT-PCR)检测标本的miR-181a,Western blot检测ATM蛋白。比较胃癌组织及癌旁非癌组织中miR-181a、ATM蛋白表达量。 结果 miR-181a在胃癌组织中的表达量为(1.981±1.800),miR-181a在邻近非癌组织中的表达量为(0.394±0.093);灰度值检测:癌组织ATM蛋白为(0.2539±0.0046);非癌组织为(0.5525±0.0660),癌及非癌组织中miR-181a、ATM蛋白表达量比较,差异均有高度统计学意义(P 0.01);miR-181a与ATM蛋白表达呈负相关(r=-0.539,P 0.01)。 结论 miR-181a在胃癌组织中表达明显增高,ATM蛋白表达明显下降;究其原因可能是通过基因沉默机制miR-181a降低ATM蛋白表达量,从而在胃癌的发生及发展中起促进作用。   [关键词] 共济失调-毛细血管扩张突变基因;胃癌;微小RNA;miR-181a   [中图分类号] R735.2 [文献标识码] A [文章编号] 1673-7210(2015)05(c)-0024-05   [Abstract] Objective To investigate the expression and significance of microRNA (miRNA)-181a (miR-181a) and its target gene ATM in gastric carcinoma tissues. Methods Tissues of gastric carcinoma and adjacent non-tumorous were collected respectively from 9 patients given surgical operation in Guangzhou First Peoples Hospital from April 2009 to December 2011. The total RNA and protein were extracted routinely, the miR-181a was detected by Real-time quantitative PCR, ATM protein was detected by Western blot. The expression of miR-181a and ATM protein between gastric carcinoma and adjacent non-tumorous were compared, and the correlation between miR-181a and ATM protein levels in gastric carcinoma was analyzed. Results In gastric carcinoma tissues, the expression of miR-181a and ATM protein were (1.981±1.800), (0.2539±0.0046) respectively, whereas in the adjacent non-tumorous tissues, the expression of miR-181a and ATM protein were (0.394±0.093), (0.5525±0.0660) respectively. The differences between the expression of miR-181a and ATM protein in these two tissues were statistically significant (P 0.01). There was a negative correlation between miR-181a and ATM protein levels (r=-0.539, P 0.01). Conclusion The expression of miR-181a is significantly up-regulat

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