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作 者:张俊和[1] 张军[2] 杨东波[1] 李洋[1] 明键光[1] 韩煊烨[1] 蒋传路[1]
机构地区:[1]哈尔滨医科大学附属第二医院神经外科,150086 [2]齐齐哈尔市第一医院神经外科,161000
出 处:《中国微侵袭神经外科杂志》2015年第1期33-36,共4页Chinese Journal of Minimally Invasive Neurosurgery
基 金:黑龙江省卫生厅科研课题(编号:2013048);黑龙江省自然科学基金面上项目(编号:H201417)
摘 要:目的探讨mi R-410在胶质瘤细胞的作用机制。方法收集50例人胶质瘤标本以及胶质母细胞瘤U251和U87细胞系。采用mi Randa靶基因预测软件对mi R-410的靶基因预测分析,初步判断其与MET基因的相关性;利用免疫组化和原位杂交技术检测人脑胶质瘤标本中mi R-410和MET的表达;荧光素酶报告基因实验检测mi R-410对MET的靶向作用;Western blot检测mi R-410模拟物转染肿瘤细胞后MET蛋白的变化。结果经mi Randa靶基因分析:MET m RNA的3’非编码区(3’UTR)与mi R-410的种子序列存在理论上的互补匹配序列。免疫组化和原位杂交技术检测:肿瘤标本中mi R-410和MET具有负相关性(r=-0.69783,P<0.001)。荧光素酶实验进一步证实胶质母细胞瘤中MET基因是mi R-410的直接靶点。肿瘤细胞转染mi R-410模拟物后对MET蛋白的表达具有明显的抑制作用(P<0.05)。结论在胶质瘤细胞中mi R-410靶向作用MET,可能是胶质瘤治疗的新靶点。Objective To explore the functional mechanism of miR-410 in glioma cells.Methods Fifty human glioma samples and glioblastoma cell lines U251 and U87 were collected.The genetic analysis of correlation of miR-410 and MET gene was judged by the miRanda target gene prediction software.Immunohistochemistry and in situ hybridization technique were used to confirm the expressions of miR-410 and MET in the human brain glioma samples.Further,Luciferase experimental method was used to test the targeting effect of miR-410 on MET.Western blot was used to detect the change of MET protein after the transfection of miR-410 analogue into U87 and U251 tumor cells.Results The matching sequences between 3'untranslated region(3'UTR) of MET m RNA and seed sequences of miR-410 existed theoretically,which were confirmed by miRanda target gene analysis.The negative correlation of miR-410 and MET in tumor samples was confirmed by immunohistochemistry and in situ hybridization(r =-0.69783,P〈0.001).Luciferase experiments further confirmed that MET gene was the direct target of miR-410 in human glioblastoma.After the tumor cells were transfected with miR-410 simulation,the MET expression was inhibited significantly(P〈0.05).Conclusion miR-410 targets on MET in gliomas,and may be the new target for glioma treatment.
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