文章摘要
吴 兵,李世升,肖商荣,马书元,张亚飞.CD47-siRNA通过调控ROS诱导食管癌细胞SEG-1凋亡[J].,2019,19(11):2061-2065
CD47-siRNA通过调控ROS诱导食管癌细胞SEG-1凋亡
CD47-siRNA Induces the Apoptosis of Esophageal Cancer Cells SEG-1 by Regulating ROS
投稿时间:2018-11-28  修订日期:2018-12-23
DOI:10.13241/j.cnki.pmb.2019.11.012
中文关键词: CD47-siRNA转染  食管癌细胞SEG-1  凋亡  活性氧簇
英文关键词: CD47-siRNA  Esophageal cancer cells SEG-1  Apoptosis  Reative oxygen species
基金项目:国家自然科学基金项目(81701501)
作者单位
吴 兵 陕西省核工业215医院内镜科 陕西 咸阳 712000 
李世升 陕西省核工业215医院内镜科 陕西 咸阳 712000 
肖商荣 陕西省核工业215医院内镜科 陕西 咸阳 712000 
马书元 陕西省核工业215医院内镜科 陕西 咸阳 712000 
张亚飞 陕西省核工业215医院内镜科 陕西 咸阳 712000 
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中文摘要:
      摘要 目的:探讨CD47-siRNA对食管癌细胞SEG-1凋亡的影响及其机制研究。方法:Western blot法检测食管癌细胞SEG-1中CD47蛋白、促凋亡蛋白Bax和抗凋亡蛋白Bcl-2的表达;CCK-8法检测食管癌细胞SEG-1细胞活力;DCFDA细胞ROS检测试剂盒检测食管癌细胞SEG-1 中ROS水平。结果:CD47-siRNA转染组食管癌细胞SEG-1中CD47蛋白明显低于空载对照组(P< 0.05);CD47-siRNA转染组食管癌细胞SEG-1细胞活力显著低于空载对照组(P<0.05);CD47-siRNA转染组食管癌细胞SEG-1中促凋亡蛋白Bax表达显著高于空载对照组(P<0.05),抗凋亡蛋白Bcl-2表达低于空载对照组(P<0.05);CD47-siRNA转染食管癌细胞SEG-1组ROS水平明显高于空载对照组(P< 0.05);与CD47-siRNA转染组比较,CAT (ROS抑制剂,5 mM/L, 6 h) 预处理增加了细胞活力;与CD47-siRNA转染组比较,CAT (ROS抑制剂,5 mM/L, 6 h)预处理显著降低食管癌细胞SEG-1中Bax蛋白表达以及增加抗凋亡蛋白Bcl-2表达。结论:CD47-siRNA转染通过上调食管癌细胞SEG-1内ROS水平促进食管癌细胞SEG-1凋亡。
英文摘要:
      ABSTRACT Objective: To detect the effects of CD47-siRNA on the apoptosis of esophageal cancer cells SEG-1 and its mechanism. Methods: Western blot was used to detect the CD47 protein, pro-apoptosis Bax and anti- apoptosis Bcl-2; Cell Counting Kit-8(CCK-8)was used to detect cell viability; DCFDA cellular ROS detection kit was used to detect the ROS level of esophageal cancer cells SEG-1. Results: CD47 protein in CD47-siRNA transfected group was significantly lower than Vector-NC group (P<0.05). The cell viability in CD47-siRNA transfected group was significantly lower than Vector-NC group (P<0.05). The expression of pro-apoptotic protein Bax in CD47-siRNA transfected group was significantly higher than Vector-NC group (P<0.05), and the expression of anti-apoptotic protein bcl-2 was lower than Vector-NC group (P<0.05). The ROS level in CD47-siRNA transfected group was significantly higher than Vector- NC group (P<0.05). Compared with CD47-siRNA transfected group, pretreatment with CAT (ROS inhibitor, 5 mm /L, 6 h) increased the cell viability. Compared with CD47-siRNA transfected group, pretreatment with CAT (ROS inhibitor, 5 mm/L, 6 h) significantly reduced the expression of Bax protein and increased the expression of Bcl-2 protein. Conclusion: CD47-siRNA can promote the apoptosis of esophageal cancer cells SEG-1 through increasing the level of ROS in esophageal cancer cells SEG-1.
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