| 沉默VEGF对人鼻咽癌放射抗拒细胞株CNE-2R侵袭迁移的影响 |
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| 引用本文： | 陈莉,林国享,陈凯华,孙永楚,万芳竹,朱小东.沉默VEGF对人鼻咽癌放射抗拒细胞株CNE-2R侵袭迁移的影响[J].中国癌症防治杂志,2019,11(6):474-479. |
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| 作者姓名： | 陈莉 林国享 陈凯华 孙永楚 万芳竹 朱小东 |
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| 作者单位： | 广西医科大学附属肿瘤医院放疗科；广西医科大学附属武鸣医院肿瘤科 |
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| 基金项目： | 国家自然科学基金项目（81760544）；广西高校中青年教师科研基础能力提升项目（2019KY0115）；广西医科大学青年科学基金项目（GXMUYSF201720） |
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| 摘 要： | 目的 探讨沉默血管内皮生长因子（vascular endothelial growth factor，VEGF）对人鼻咽癌放射抗拒细胞株CNE-2R迁移和侵袭能力的影响。方法 制备含VEGF-shRNA的慢病毒载体（VEGF-LV1、VEGF-LV2、VEGF-LV3）和对照shRNA重组慢病毒（VEGF-NC），并转染人鼻咽癌放射抗拒细胞株CNE-2R，建立稳定沉默VEGF细胞（CNE-LV1、CNE-LV2和CNE-LV3）和阴性对照细胞（CNE-NC）。采用RT-qPCR和Western blot法检测细胞转染效果，划痕实验和Transwell小室实验检测VEGF沉默后细胞的迁移和侵袭能力。结果 成功构建VEGF-shRNA重组慢病毒并建立了稳定沉默VEGF细胞CNE-LV3。划痕实验和Transwell小室迁移实验显示，与空白对照组和CNE-NC组相比，CNE-LV3组细胞迁移率明显降低［（50.17±1.76）% vs （37.97±1.56）%，P＝0.001；（50.63±1.52）% vs （37.97±1.56）%，P＝0.001］，穿膜细胞数亦明显下降［（95.3±3.8） 个 vs （41.3±1.5） 个，P＜0.001；（94.3±4.0） 个 vs （41.3±1.5） 个，P＜0.001］；Transwell小室侵袭实验结果亦显示，CNE-LV3组细胞穿膜细胞数较空白对照组和CNE-NC组明显下降［（46.3±2.1） 个 vs（105.3±1.5） 个，P＜1.001；（46.3±2.1） 个 vs （93.3±2.5） 个，P＜0.001］。结论 沉默VEGF表达可抑制人鼻咽癌放射抗拒细胞株CNE-2R的迁移和侵袭能力。
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Effect of silencing
VEGF on the invasion and migration of radioresistant human nasopharyngeal
carcinoma cell line CNE-2R |
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| CHEN Li,LIN Guoxiang,CHEN Kaihua,SUN Yongchu,WAN Fangzhu,ZHU Xiaodong.Effect of silencing
VEGF on the invasion and migration of radioresistant human nasopharyngeal
carcinoma cell line CNE-2R[J].Chinese Journal of Oncology Prevention and Treatment,2019,11(6):474-479. |
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| Authors: | CHEN Li LIN Guoxiang CHEN Kaihua SUN Yongchu WAN Fangzhu ZHU Xiaodong |
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| Abstract: | Objective To investigate the effect of silencing the gene of VEGF on the migration and invasion of radioresistant human nasopharyngeal carcinoma cell line CNE-2R. Methods Three groups of lentiviral vectors containing VEGF-shRNA （VEGF-LV1，VEGF-LV2，VEGF-LV3） and control shRNA recombinant lentivirus（VEGF-NC） were prepared. Cells of radio resistant human nasopharyngeal carcinoma CNE-2R were transfected to establish a cell line stably silencing VEGF expression（CNE-LV1，CNE-LV2，and CNE-LV3），and a negative control group（NE-NC） was established. RT-qPCR and Western blot were used to detect the infection effect of each group. Scratch test and Transwell chamber assay were used to detect cell migration and invasion after VEGF silencing. Results VEGF-shRNA recombinant lentivirus were successfully constructed and the stable subcellular cell line（CNE-LV3）with VEGF silencing was established. The scratch test showed that the cell migration rate of the CNE-LV3 group was significantly lower than that of the blank control group and the CNE-NC group［（37.97±1.56）% vs （50.17±1.76）%，P＝0.001；（37.97±1.56）% vs （50.63±1.52）%，P＝0.001］. Transwell chamber migration assay showed that the number of transmembrane cells in the CNE-LV3 group was significantly decreased compared with the blank control group and CNE-NC group（41.3±1.5 vs 95.3±3.8，P＜0.001； 41.3±1.5 vs 94.3±4.0，P＜0.001）. And Transwell chamber invasion assay also showed that the number of transmembrane cells in the CNE-LV3 group was significantly decreased compared with the blank control group and CNE-NC group（46.3±2.1 vs 105.3±1.5，P＜0.001；46.3±2.1 vs 93.3±2.5，P＜0.001）. Conclusion Silencing VEGF expression can inhibit the migration and invasion of radioresistant human nasopharyngeal carcinoma cell line CNE-2R. |
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| Keywords: | Nasopharyngeal carcinoma VEGF Lentivirus Radioresistant Invasion Migration |
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