基础医学与临床 ›› 2017, Vol. 37 ›› Issue (2): 197-201.

• 研究论文 • 上一篇    下一篇

miR-210对肾透明细胞癌血管生成的影响

朱国栋,杨龙,田野   

  1. 天津医科大学总医院
  • 收稿日期:2016-06-14 修回日期:2016-11-04 出版日期:2017-02-05 发布日期:2017-01-16
  • 通讯作者: 杨龙 E-mail:yanglonghospital@163.com
  • 基金资助:
    脑源性微粒在颅脑创伤相关凝血功能障碍发生中的机制研究

Effect of miR-210 on angiogenesis of renal clear cell carcinoma

  • Received:2016-06-14 Revised:2016-11-04 Online:2017-02-05 Published:2017-01-16

摘要: 目的 探讨miR-210对肾透明细胞癌血管生成的影响。方法 检测40例肾透明细胞癌组织标本中miR-210的表达,并分析其与相应癌组织中微血管密度(MVD)的关系。通过miR-210反义寡核苷酸(miR-210-ASO)技术抑制肾透明细胞癌细胞系786-O细胞中miR-210表达,RT-qPCR检测转染效果。三维培养实验观察对照组、阴性对照组和miR-210-ASO组肿瘤细胞上清液对人脐静脉内皮细胞(HUVEC)管腔形成数量的影响。建立裸鼠移植瘤模型,应用endomucin免疫荧光染色于激光共聚焦显微镜下观察抑制miR-210对移植瘤生长,血管形成和VEGF表达的影响。结果 肾透明细胞癌组织标本中miR-210的表达与微血管密度呈正相关(P<0.05),经miR-210-ASO转染的786-O细胞其miR-210表达明显下降(P<0.05)。miR-210-ASO组细胞上清液培养的HUVEC细胞管腔形成数量显著少于对照组和阴性对照组(P<0.05)。miR-210-ASO组细胞形成的移植瘤体积小于对照组,且微血管数量和VEGF的表达量显著少于对照组(P<0.05)。结论 抑制miR-210可降低肾透明细胞癌中血管生成数量。

关键词: miR-210, 肾透明细胞癌, 血管生成

Abstract: Objective To investigate the effect ofmiR-210 on angiogenesis of human renal clear cell carcinoma. Methods Detect the expression of miR-210 in 40 cases of renal clear cell carcinoma tissues, and analyze the relationship between the expression of miR-210 and microvessel density (MVD). MiR-210-ASO was lipotransfected into renal clear cell carcinoma cell line 786-O. RT-qPCR to verify the transfection effect. The effect of the supernatant of control group, negative control group and miR-210-ASO group tumor cells on the lumen formation of human umbilical vein endothelial cells (HUVEC) was observed in three dimensional culturesystems. The transplantation tumor model of nude mice was established, and the effect of miR-210 on the formation of the transplanted tumor micro vesselwas observed by endomucinand VEGF immunofluorescence staining under laser scanning confocal microscope. Results The expression of miR-210 was positively correlated with microvessel density in renal clear cell carcinoma (P<0.05).The expression of miR-210 was significantly decreased in 786-O cells transfected with miR-210-ASO(P<0.05). The lumen formation of HUVEC cells co cultured with miR-210-ASO group cell supernatant was significantly less than that of control group and negative control group(P<0.05). The tumor volume of miR-210-ASO group was less than that of the control group, and the number of the micro vesseland the VEGF expression were significantly less than that of the control group (P<0.05). Conclusions Inhibition of miR-210 can suppress the ability of blood vessel formation in renal clear cell carcinoma.

Key words: miR-210, renal clear cell carcinoma, Angiogenesis

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