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作 者:胡那日苏[1] 张斌[1] 俞春江[2] 关呈超[3] 朴松林[3] 孙瑶[3] 许丽丽[3] 王丽娜[1]
机构地区:[1]哈尔滨医科大学第二临床医学院口腔颌面外科,黑龙江哈尔滨150086 [2]哈尔滨医科大学第二临床医学院神经内科,黑龙江哈尔滨150086 [3]哈尔滨医科大学口腔医学院口腔颌面外科,黑龙江哈尔滨150001
出 处:《口腔颌面外科杂志》2009年第1期23-27,共5页Journal of Oral and Maxillofacial Surgery
摘 要:目的:研究三氧化二砷(As2O3)对人类腺样囊性癌ACC-M细胞体外增殖及表达VEGF和bFGF的影响。探讨As2O3对ACC-M细胞表达VEGF和bFGF的影响。方法:倒置相差显微镜下观察ACC-M细胞生长情况,采用MTT法检测不同浓度As2O3作用不同时间对ACC-M的抑制效应;以RT-PCR、Western blot方法检测As2O3作用后ACC-M细胞的两种血管生成相关因子VEGF和bFGF表达的变化。结果:As2O3抑制ACC-M细胞呈时间-剂量依赖关系。RT-PCR检测显示,As2O3作用后ACC-M细胞VEGF和bFGF基因表达无明显变化。Western blot检测显示,As2O3明显抑制ACC-M细胞VEGF和bFGF蛋白表达,呈时间-剂量依赖关系。结论:As2O3在体外明显抑制ACC-M细胞;As2O3明显抑制ACC-M细胞VEGF和bFGF基因的蛋白产物,其作用机制可能为抗腺样囊性癌的血管形成。Objective: The aim of this study was to investigate the proliferation effects of As2O3 on salivary adenoid cystic carcinoma-M (ACC-M) cells in vitro and gene expression of VEGF and bFGF within those cells. The possible mechanism of As2O3 on gene expression of VEGF and bFGF was also elucidated. Methods: ACC-M ceils were treated with different concentration of As2O3 for different time. Cytomorphology of ACC-M cells was observed on phasecontrast microscope. Proliferation or suppression effect on cells' viability was detected by MTT method. Gene and protein expression of VEGF and bFGF were investigated by RT-PCR and Western blot analysis respectively. Results: Cell viability after As2O3 treatment was markedly suppressed and exhibited as a dose- and time-dependent pattern. RT-PCR revealed no statistically difference between gene expression of VEGF and bFGF. Through Western blot analysis, a negative correlation between As2O3 concentration and amount of protein product of these two cytokines was determined. Conclusions: As2O3 might markedly suppressed ACC-M cells' viability with a time-dose reliable pattern in vitro. As2O3 decreases protein product of VEGF and bFGF apparently. Therefore, the agent might suppress vessel formation of ACC-M cells.
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