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作 者:李晓霞[1] 郭红荣[1] 韦国桢[1] 曹琦[1]
机构地区:[1]南京医科大学附属常州第二人民医院呼吸内科,江苏常州213003
出 处:《海南医学院学报》2009年第12期1477-1480,1484,共5页Journal of Hainan Medical University
基 金:常州市卫生局科技计划资助项目项目编号:(2004102)~~
摘 要:目的:研究三氧化二砷(arsenic trioxide,As2O3)对肺腺癌A549细胞株细胞增殖、细胞周期以及cylin D1基因表达情况,初步探讨As2O3对肺腺癌细胞增殖的影响及其机制。方法:分别以不同浓度的As2O3作用于A549细胞,作用不同时间后,对细胞增殖活性、细胞周期及cylin D1基因表达的情况进行检测。结果:稍高浓度(>2μmol/L)的As2O3可抑制A549细胞增殖,并有剂量和时间依赖性,As2O3可抑制A549细胞由G1期进入S期。逆转录聚合酶链式反应(RT-PCR)检测cylin D1基因转录水平和细胞爬片免疫组化检测cyclin D1基因蛋白表达的相对强度,发现As2O3作用组cyclin D1基因表达与对照组相比明显减低(P<0.01)。结论:As2O3可有效抑制A549细胞增殖,抑制效应呈量效和时效关系,并且能阻碍细胞周期由G1进入S期,这一过程可能与As2O3抑制cyclin D1基因表达有关。Objective:To investigate the effects of arsenic trioxide (As2O3) on the proliferation,cycle of A549 cells and gene expression of cyclin D1 in lung adenocarcinoma and its mechanism. Methods: A549 cells were treated with different dosages of As2O3 for different periods of time,then its proliferation,cell cycle and the gene expression of cyclin D1 were detected and analyzed. Results: Being applied at the dosage of 〉2 μmol/L,As2 03 showed a dose and time dependent inhibition on the proliferation of A549 cells. Cell cycle arrest at G0/G1 in A549 cells can also be provoked by As203. The reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemistry detection revealed that the gene expression of cyclin D1 was significantly downregulated in As203 treated group(P 〈0.01 ). Conclusion: As203can induce an dose and time dependent inhibition on the pro- liferation of A549 ceils. It can also provoke cell cycle arrest at G0/G1 stage which may be related with its function of depressing cyclin D1 gene expression.
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