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作 者:赵晓静[1] 马军[1] 袁翎[2] 王昆仑[2] 李南[3] 张中冕[3] 孙佳[3]
机构地区:[1]郑州大学第二附属医院消化内科,郑州450014 [2]郑州大学附属肿瘤医院河南省肿瘤医院放疗科,郑州450014 [3]郑州大学第二附属医院肿瘤科,郑州450014
出 处:《郑州大学学报(医学版)》2017年第3期247-250,共4页Journal of Zhengzhou University(Medical Sciences)
基 金:河南省科技厅科技攻关项目152300410164
摘 要:目的:探讨食管鳞癌细胞系TE7放射照射后miRNAs及DNA修复相关因子表达的关系。方法:采用实时定量PCR检测不同剂量(0、2、4、6、8 Gy)X射线照射后TE7中miR-126、miR-21、miR-101、DNA-PKcs mRNA及RAD21 mRNA的表达,蛋白免疫印迹法检测DNA-PKcs和RAD21蛋白的表达。结果:X射线照射后,随吸收剂量的增加,TE7中miR-126表达逐渐升高(P<0.05),miR-101表达降低(P<0.05),DNA-PKcs和RAD21 mRNA表达逐渐升高(P<0.05);磷酸化DNA-PKcs、总DNA-PKcs及RAD21蛋白表达无明显变化(P>0.05)。当吸收剂量是4Gy时,TE7细胞中miR-126、miR-101与RAD21蛋白表达呈负相关(r分别为-0.899、-0.853,P均<0.05)。结论:miR-126及miR-101可能通过调节RAD21的表达影响TE7细胞的放疗敏感性。Aim: To explore the expressions of miRNAs and DNA repair factors in esophageal squamous cell carcinoma cell line TE7 after radiation. Methods: Real-time PCR was used to detect the expressions of miR-126,miR-21,miR-101,DNA-PKcs,and RAD21 mRNA in TE7 cells treated with different doses( 0,2,4,6,8 Gy) of X-ray radiation,and Western blot was used to detect the expressions of DNA-PKcs and RAD21 protein. Results: In TE7 cells treated with Xray radiation,the expressions of miR-126,DNA-PKcs and RAD21 mRNA were up-regulated with the dose increasing( P 〈0. 05),that of miR-101 was down-regulated( P 〈 0. 05),and the expressions of phospho-DNA-PKcs,total DNA-PKcs and RAD21 protein had no statistical changes( P 〉 0. 05). The expressions of miR-126 and miR-101 were negatively correlated with that of RAD21 protein( r =-0. 899,-0. 853,P 〈 0. 05) in TE7 cells treated with 4 Gy radiation. Conclusion: MiR-126 and miR-101 may influence the radio-sensitivity of TE7 cells by regulating the expression of RAD21.
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