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机构地区:[1]辽宁医学院附属第一医院肿瘤科,辽宁锦州121001 [2]中国医学科学院放射医学研究所
出 处:《肿瘤防治研究》2011年第1期13-16,共4页Cancer Research on Prevention and Treatment
摘 要:目的利用shRNA抑制Ku80蛋白表达来研究Ku80对人食管癌细胞黏附、侵袭能力的影响。方法用Western blot和RT-PCR方法证实RNA干扰的有效性和可行性。用细胞黏附实验、细胞侵袭实验来研究Ku80基因沉默对人食管癌细胞黏附、侵袭能力的影响。结果干扰载体shR-NA-H2,K3抑制Ku80蛋白的表达,抑制率分别为63%和50%(P<0.01),且抑制Ku80mRNA的含量,达84%和58%(P<0.01)。同时,干扰载体shRNA-H2,K3抑制人食管癌细胞的黏附率分别(63.19±4.93)%和(52.87±2.67)%及抑制人食管癌细胞的侵袭能力,抑制率为69.6%和62.1%(P<0.01)。结论 Ku80在食管癌的侵袭及转移过程中起作用,Ku80基因沉默有望成为肿瘤基因治疗的一个靶点。Objective To investigate the effects of Ku80 on cell adhesion and invasion of human esophageal carcinoma cells by using shRNA vector to evoluate the inhibition of Ku80 expression.Methods The effectiveness and feasibility of RNA interference were confirmed by Western blot and RT-PCR methods.Effects of silencing Ku80 gene on cell adhesion and invasion of esophageal carcinoma cells were investigated by cell adhesion assay and cell invasion assay,respectively.Results The express of Ku80 protein was reduced by shRNA-H2 and K3.The inhition rate was 63% and 50% for shRNA-H and K3,respectively(P0.01).Content of Ku80 mRNA was reduced by shRNA-H2 and K3,respectively to 84% and 58%(P0.01).Adhesion rate of human esophageal carcinoma cells was inhibited by shRNA-H2 and K3,respectively(63.19±4.93)% and(52.87±2.67)%.Cell invasion was inhibited by shRNA-H2 and K3.Its inhibiton rate was 69.6% and 62.1%(P0.01),respectively.Conclusion Ku80 plays a role in invasion and migration of esophageal cancer.The inhibition of Ku80 expression was induced by shRNA,which means that silencing Ku80 gene may become a target of gene therapy to tumor.
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