摘要
目的探讨miR-140-5p介导Jagged1对肾透明细胞癌(ccRCC)迁移、侵袭及血管生成能力的影响。方法选取福建省漳州市医院泌尿外科2019年4月至2020年12月经肾癌根治术患者的肾透明细胞癌及癌旁组织标本17例, 选取购自美国菌种保藏中心肾透明细胞癌细胞系(786-0)和肾皮质近曲小管上皮细胞(HK-2), 荧光定量聚合酶链反应(RT-qPCR)检测miR-140-5p的表达。免疫组织化学检测ccRCC组织中Jagged1的表达。将786-0细胞分为miRNA阴性对照组(miR-NC组)、过表达miR-140-5p组(miR-140-5p组)、Jagged1阴性对照组(Jagged1-NC组)、敲减Jagged1组(si-Jagged1组)。使用划痕、transwell小室和血管生成实验, 分别检测细胞迁移、侵袭和血管生成的改变。RT-qPCR检测miR-140-5p过表达后Jagged1 mRNA的表达, 蛋白质印迹法(Western blot)检测Notch/Jagged1信号通路中Jagged 1蛋白的表达。计量资料比较采用t检验, 计数资料采用χ^(2)检验。结果 ccRCC组织(0.318±0.144)中miR-140-5p的表达量显著低于正常肾组织(1.028±0.033), 差异有统计学意义(t=-19.787, P<0.01);786-0肾癌细胞(0.295±0.064)中miR-140-5p的表达量显著低于HK-2正常肾细胞(1.009±0.157), 差异有统计学意义(t=-8.366, P<0.01);在体外, miR-140-5p组的细胞迁移率(0.394±0.015)、侵袭细胞数(142.000±17.874)和血管管腔样结构的形成数(46.000±5.291)显著少于miR-NC组的细胞迁移率(0.548±0.020)、侵袭细胞数(267.000±26.357)和血管管腔样结构的形成数(74.000±8.000), 差异有统计学意义(t=-10.362、-14.445、-5.056, P<0.01);与miR-140-5p相反, ccRCC组织中Jagged1的表达(92.30%)显着高于正常肾组织(36.67%), 差异有统计学意义(χ^(2)=5.356, P<0.05);si-Jagged1组的细胞迁移率(0.429±0.011)、侵袭细胞数(130.533±19.379)和血管管腔样结构的形成数(45.333±3.214, )都显著少于Jagged1-NC组的细胞迁移率(0.495±0.025)、侵袭细胞数(252.466±19.231)和血管管腔样结构的形成数(66.000±3.605), 差异有统计学意义(t=-3.999、-17.297、-7.410, P<0.05);miR-140-5p组中Jagged1 mRNA的相对表达量(0.434±0.150)显著低于miR-NC组(1.026±0.265), 差异有统计学意义(t=-3.425, P<0.05)。miR-140-5p组(0.336±0.159)中Jagged1蛋白的表达较miR-NC组(0.900±0.121)降低, 差异有统计学意义(t=-4.901, P<0.01)。结论 miR-140-5p可抑制ccRCC的进展, miR-140-5p可能下调Jagged1抑制ccRCC迁移、侵袭及血管生成。
Objective To investigate the effects of microRNA(miR)-140-5p mediated Jagged1 on migration,invasion and angiogenesis of renal clear cell carcinoma(ccRCC).Methods Totally,17 cases of ccRCC and renal tissue samples were selected.The ccRCC cell line(786-0)and renal cortical proximal tubular epithelial cells(HK-2)were selected and the expression of miR-140-5p was detected by fluorescence quantitative polymerase chain reaction(RT-qPCR).The expression of Jagged1 in ccRCC tissues was detected by immunohistochemistry.The 786-0 cells were divided into miRNA negative control group(miR-NC group),overexpression miR-140-5p group(miR-140-5p group),Jagged1 negative control group(Jagged1-NC group),and knockdown Jagged1 group(si-Jagged1 group).Using scratch,Transwell inserts and angiogenesis assays,alterations in cell migration,invasion and angiogenesis were detected,respectively.The expression of Jagged1 mRNA after miR-140-5p overexpression was detected by RT-qPCR,and the expression of Jagged 1 protein in the Notch/Jagged1 signaling pathway was detected by Western blotting.Measurement data were compared using the t-test,and enumeration data were analyzed using theχ^(2) test.Results The expression of miR-140-5p in ccRCC tissues(0.318±0.144)was significantly lower than that in normal renal tissues(1.028±0.033),and the difference was statistically significant(t=-19.787,P<0.01);the expression of miR-140-5p in 786-0 renal carcinoma cells(0.295±0.064)was significantly lower than that in HK-2 normal renal cells(1.009±0.157),and the difference was statistically significant(t=-8.366,P<0.01);in vitro,the cell migration rate(0.394±0.015),the number of invasive cells(142.000±17.874),and the number of vascular tube-like structure formation(46.000±5.291)in the miR-140-5p group were significantly reduced as compared with those in the miR-NC group(0.548±0.020,267.000±26.357 and 74.000±8.000 respectively),and the difference was statistically significant(t=-10.362,-14.445,-5.056,P<0.01);in contrast to miR-140-5p,the expression rate of Jagged1 in ccRCC tissues(92.30%)was significantly higher than that in normal renal tissues(36.67%),and the difference was statistically significant(χ^(2)=5.356,P<0.05);the cell migration rate(0.429±0.011),the number of invasive cells(130.533±19.379)and the formation of vascular tube-like structures(45.333±3.214)in the si-Jagged1 group were significantly reduced as compared with those in the Jagged1-NC group(0.495±0.025,252.466±19.231 and 66.000±3.605,respectively),and the difference was statistically significant(t=-3.999,-17.297,-7.410,P<0.05);The relative expression of miR-140-5p Jagged1 mRNA(0.434±0.150)was significantly lower than that of the miR-NC group(1.026±0.265),and the difference was statistically significant(t=-3.425,P<0.05).The expression of Jagged1 protein was decreased in the miR-140-5p group(0.620±0.000)as compared with the miR-NC group(0.991±0.013),and the difference was statistically significant(t=-39.389,P<0.05).Conclusion MiR-140-5p can inhibit the progression of ccRCC,and miR-140-5p may down-regulate Jagged1 to inhibit ccRCC migration,invasion and angiogenesis.
作者
吴国森
徐林熙
许振强
林建贵
刘洪杰
庄志明
Wu Guosen;Xu Linxi;Xu Zhenqiang;Lin Jiangui;Liu Hongjie;Zhuang Zhiming(Department of Urology,Zhangzhou Municipal Hospital,Zhangzhou 363000,China)
出处
《中华实验外科杂志》
CAS
北大核心
2022年第6期1038-1041,共4页
Chinese Journal of Experimental Surgery
关键词
微小RNA
肾癌
迁移
侵袭
血管生成
MicroRNA
Renal carcinoma
Migration
Invasion
Angiogenesis