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机构地区:[1]深圳市第二人民医院呼吸内科,广东深圳518035 [2]广东医学院附属医院呼吸内科 [3]广东医学院呼吸疾病研究所,广东湛江524001
出 处:《现代肿瘤医学》2012年第9期1779-1783,共5页Journal of Modern Oncology
摘 要:目的:研究亚砷酸钠(NaAsO2)对人肺癌Spc-A1细胞株端粒酶活性及其催化亚单位hTERT表达的影响,探讨其抗癌机制。方法:四甲基偶氮唑蓝法(MTT)检测亚砷酸钠对Spc-A1细胞增殖的抑制作用;端粒酶活性采用端粒末端重复序列扩增-酶联免疫吸附法(TRAP-ELISA)测定;端粒酶催化亚单位hTERT-mRNA表达采用反转录聚合酶链式反应法(RT-PCR)测定。结果:亚砷酸钠对人肺癌细胞株Spc-A1的增殖具有一定程度的抑制作用。在12h、24h和48h三个时间段均可见Spc-A1细胞端粒酶活性随着药物浓度的增加逐渐下降。并且,hTERT mRNA表达下调与端粒酶活性下降一致。结论:亚砷酸钠对Spc-A1细胞的增殖具有一定的抑制作用,下调癌细胞hTERT mRNA的表达来抑制端粒酶活性可能是其中一种机制。Objective:To investigate the posssible anticarcinogenic mechanisms by studying the effect of sodium arsenite ( NaAsO2 ) on telomerase activity and human telomerase reverse transcriptase (hTERE) gene expression of hu- man lung carcinoma Spe - A1 cells. Methods:MTT( Methyl Thiazolyl Tetrazolium)assay was used to determine the growth inhibition by sodium arsenite in Spe - A1 cells. Telomerase activity was examined by telomeric repeat amplifi-cation protocol ELISA( TRAP - ELISA). Expression of hTERE was assessed by reverse transcription polymerase chain reaction (RT -PCR). Results: NaAsO2 could inhibit the proliferation of Spc -A1 cells in some degree. Elomerase ac-tivity of Spc - A1 cells was declined gradually when the concentrations of NaAsO2 increased from 1 μg/ml to 2μg/ml to 4μg/ml during the period of 12h ,24h and 48h respectively. And the down - regulation of expression of hTERTmR- NA was consistent with the change of telomerase activity. Conclusion : Sodium arsenite could obviously inhibit the pro- liferation of SPC - A - 1 cell. The inhibition of telomerase activity through decreasing expression of hTERT may be one of meehanisms.
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