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机构地区:[1]第三军医大学附属新桥医院普通外科,重庆400037 [2]第三军医大学附属新桥医院神经外科,重庆400037 [3]中国医学科学院药物研究所,北京100050
出 处:《癌变.畸变.突变》2011年第2期111-113,133,共4页Carcinogenesis,Teratogenesis & Mutagenesis
摘 要:目的:在成功构建人COX-2基因反义真核表达载体的基础上,研究COX-2基因对人胃癌细胞株SGC-7901转移能力的影响。方法:实验分为COX-2基因反义真核表达载体转染的人胃癌细胞株SGC-7901转染组、COX-2抑制剂SC236处理组(SGC-7901细胞培养基内含100μmol/L SC236)和对照组(SGC-7901细胞),并分别采用细胞体外侵袭实验,内皮细胞体外迁移实验,观察各组细胞体外转移的情况。采用裸鼠皮下移植瘤抑制实验,用转染和未转染的SGC-7901细胞按每毫升5×10~7个的细胞悬液分别注射于BALB/C-nu/nu无胸腺裸鼠背部皮下,SC236处理组按3mg/(kg·d)剂量于接种SCC-7901细胞10min后,由尾静脉注射,隔日1次。各组6周后处死动物,观察皮下移植瘤的生长情况。并用Western blot法检测各组细胞VEGF及MMP-2蛋白的表达。结果:体外侵袭实验、促内皮细胞体外迁移实验结果显示,与对照组相比,转染组和SC236处理组迁移的肿瘤细胞和内皮细胞均减少(P〈0.01);裸鼠皮下移植抑制实验结果显示,转染组和SC236处理组荷瘤鼠移植瘤的生长受到抑制;Western blot结果显示,转染组和SC236处理组细胞VEGF及MMP-2蛋白的表达下降。结论:反义COX-2基因能抑制SCG-7901细胞的转移能力,其机制可能与其抑制肿瘤的血管生成、减少MMP-2的表达有关。OBJECTIVE:Use constructed antisense expression vector of human COX-2 gene and observe the relationship between COX-2 gene and tumor metastasis.METHODS:Gastric cancer cell line SCG-7901 was transfected with antisense expression vector of human COX-2 gene.Three groups of cells which included transfectant、SC236 treated group(SCG-7901 treated with COX-2 inhibitor SC236 at 100μmol/L) and SCG-7901 as a control group.Changes of the invasion ability in each group were observed in vitro.Western blot was used to detect VEGF and MMP-2 expressions in the 3 groups.Then the transfectant and SCG-7901 were injected subcutaneously into BALB/Cnu /nu nude mice to develop transplantation tumor,another group of mice received SCG-7901 treated with SC236 injected subcutaneously.The sizes and the weights of the lesions were observed.RESULTS:The results of transwell membrane、cell migration and the growth of transplanted tumors showed that after transfection the invasion ability of SCG-7901 was obviously inhibited,the expressions of VEGF and MMP-2 in the cell line decreased.CONCLUSION:Transfection with antisense expression vector of human COX-2 gene had obvious antitumor activity on metastasis of human gastric cancer cell line in nude mice.The mechanism may be via inhibition of angiogenesis and down-regulation of MMP-2 expression.
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