丁 凯,尹 丽,顾佳佳.ZNF488对电离辐射诱发的鼻咽癌细胞CNE1侵袭迁移能力的影响[J].中国肿瘤,2017,26(5):395-399.
ZNF488对电离辐射诱发的鼻咽癌细胞CNE1侵袭迁移能力的影响
Effect of ZNF488 on Ionizing Irradiation-induced Migration and Invasiveness of Nasopharyngeal Cancer CNE1 Cells
投稿时间:2017-02-26  
DOI:10.11735/j.issn.1004-0242.2017.05.A014
中文关键词:  ZNF488  侵袭  迁移  电离辐射  鼻咽癌  上皮间质转化
英文关键词:ZNF488  migration  invasion  ionizing radiation  nasopharyngeal cancer  epithelial mesenchymal transition
基金项目:江苏省科技厅临床医学重点专项(BL2014091)
作者单位
丁 凯 徐州医科大学 
尹 丽 江苏省肿瘤医院江苏省肿瘤防治研究所南京医科大学附属肿瘤医院 
顾佳佳 江苏省肿瘤医院江苏省肿瘤防治研究所南京医科大学附属肿瘤医院 
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中文摘要:
      摘 要:[目的] 研究ZNF488 siRNA对电离辐射诱发的鼻咽癌CNE1侵袭迁移能力的影响。 [方法]采用qRT-PCR和Western blot检测ZNF488 siRNA转染效率。采用划痕实验和Transwell侵袭实验检测电离辐射对鼻咽癌CNE1细胞侵袭迁移能力的影响。采用划痕实验和Transwell侵袭实验检测沉默ZNF488后,电离辐射诱发的CNE1细胞侵袭迁移能力是否改变。[结果] 在mRNA和蛋白水平,实验组(siZNF488组)表达量均明显低于对照组(siRNA-Ctrl组),其中实验组ZNF488 mRNA水平为对照组的(0.54±0.12)倍(P=0.023)。划痕实验证明电离辐射明显增强鼻咽癌CNE1细胞迁移能力;Transwell侵袭实验检测到0Gy组侵袭细胞数为302.67±18.77,4Gy组侵袭细胞数为371.67±15.63,4Gy组侵袭细胞数为0Gy组(1.23±0.03)倍(P=0.006)。沉默ZNF488后,电离辐射诱发的CNE1细胞侵袭迁移能力明显减弱,这一功能的实现与上皮间质转化(EMT)进程的逆转息息相关。[结论] ZNF488 siRNA 通过逆转EMT进程抑制鼻咽癌细胞CNE1电离辐射诱发的侵袭迁移能力。
英文摘要:
      Abstract:[Purpose] To investigate the effect of ZNF488 on ionizing irradiation (IR)-induced migration and invasion in nasopharyngeal cancer CNE1 cells. [Methods] ZNF488 siRNA was transfected into CNE1 cells,the expression of ZNF488 mRNA and protein was detected by qRT-PCR and Western blot after transfection,respectively. The transfected and non-transfected CNE1 cells were exposed to 200cGy/min X-ray. The invasion and migration of CNE1 cells were analyzed by Transwell invasion assay and scratch wound healing. [Results] The mRNA expression level of ZNF488 in transfected CNE1 cells was (0.54±0.12) times as in control group (P =0.023). Transwell test showed that the number of invasion cells in 4Gy IR group(371.67±15.63) was (1.23±0.03) times higher than that of 0Gy group(302.67±18.77). The expression of ZEB1 decreased and expression of E-cadherin increased in CNE1 cells after transfected with siZNF488,while the expression of ZEB1 increased and E-cadherin decreased after 4Gy IR. [Conclusion] Silencing ZNF488 could be a new target for inhibiting metastasis caused by IR,which may be associated with regulation of IR-induced epithelial mesenchymal transition (EMT).
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