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2023 年第 11 期 第 18 卷

多瘤病毒增强活化子3和红细胞生成素产生肝细胞受体A2在脑胶质母细胞瘤中的作用

The role of polyomavirus enhancer activator 3 and erythropoietin-producing hepatocellular receptor A2 in glioblastoma of the brain

作者:麦麦提依明·托合提张诚高峰王继超吴永刚

英文作者:Mamatemin Tohti Zhang Cheng Gao Feng Wang Jichao Wu Yonggang

单位:新疆维吾尔自治区人民医院神经外科,乌鲁木齐830001

英文单位:Department of Neurosurgery People′s Hospital of Xinjiang Uygur Autonomous Region Urumqi 830001 China

关键词:胶质母细胞瘤;多瘤病毒增强活化子3;红细胞生成素产生肝细胞受体A2

英文关键词:Glioblastoma;Polyomavirusenhanceractivator3;Erythropoietin-producinghepatocellularreceptorA2

  • 摘要:
  • 目的  探讨多瘤病毒增强活化子3(PEA3)、红细胞生成素产生肝细胞受体A2(EPHA2)在脑胶质母细胞瘤中的作用。方法  构建人脑星形胶质母细胞瘤U87细胞基因转染模型,将细胞系分为5组:空白组、PEA3干扰组、PEA3干扰空载组、EPHA2干扰组、EPHA2干扰空载组。通过细胞计数试剂盒8(CCK-8)实验检测细胞增殖率,细胞划痕实验检测细胞迁移能力,Transwell实验检测细胞侵袭能力。结果  CCK-8检测细胞增殖结果显示,PEA3干扰组和EPHA2干扰组的细胞增殖率均明显低于空白组[(59.7±1.3)%、(59.5±0.7)%比(67.8±1.3)%](P<0.01或P<0.001),PEA3干扰空载组和EPHA2干扰空载组的细胞增殖率与空白组比较差异均无统计学意义(均P>0.05)。细胞划痕实验结果显示,PEA3干扰组和EPHA2干扰组的划痕愈合率低于空白组[(31.7±1.1)%、(23.0±2.6)%比(42.8±8.8)%],差异均有统计学意义(均P<0.05),PEA3干扰空载组和EPHA2干扰空载组划痕愈合率与空白组比较差异均无统计学意义(均P>0.05)。Transwell检测细胞侵袭能力结果显示,PEA3干扰组和EPHA2干扰组的侵袭细胞数明显少于空白组[(643±20)、(542±165)个比(1 225±70)个](均P<0.001),而空白组与PEA3干扰空载组和EPHA2干扰空载组侵袭细胞数比较差异均无统计学意义(均P>0.05)。结论  干扰PEA3基因和EPHA2基因能明显降低脑胶质母细胞瘤细胞的增殖、迁移、侵袭能力。

  • Objective  To investigate the role of polyomavirus enhancer activator 3(PEA3) and erythropoietin-producing hepatocellular receptor A2(EPHA2) in glioblastoma of the brain. Methods  The gene transfection model of glioblastoma U87 cells was constructed. The cell lines were divided into five groups: blank group, PEA3 interference group, PEA3 interference empty group, EPHA2 interference group and EPHA2 interference empty group. The proliferation rate was detected by cell count kit-8 (CCK-8) test, the migration ability was detected by cell scratch test, and the invasion ability was detected by Transwell test. Results  CCK-8 test showed that compared with the blank group, the cell proliferation rate of PEA3 interference group and EPHA2 interference group decreased significantly[(59.7±1.3)%, (59.5±0.7)% vs (67.8±1.3)%](P<0.01 or P<0.001). There was no significant difference between the blank group and PEA3 interference empty group and EPHA2 interference empty group in cell proliferation rate (both P>0.05). Cell scratch test showed that compared with the blank group, the cell scratch healing rate of PEA3 interference group and EPHA2 interference group decreased[(31.7±1.1)%, (23.0±2.6)% vs (42.8±8.8)%](both P<0.05). There was no significant difference between the blank group and PEA3 interference empty group and EPHA2 interference empty group in scratch healing rate (both P>0.05). Transwell test Results   showed that compared with the blank group, the number of invasive cells in PEA3 interference group and EPHA2 interference group decreased significantly [(643±20),(542±165)cells vs (1 225±70)cells](both P<0.001), and there was no significant difference between the blank group and PEA3 interference empty group and EPHA2 interference empty group(both P>0.05). Conclusion  Interference with PEA3 gene and EPHA2 gene can significantly reduce the proliferation, migration and invasion of glioblastoma of the brain.

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