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全反式维甲酸和三氧化二砷抑制子宫内膜癌细胞生长及其与NDRG1基因的关系
引用本文:陈玲,耿晓星.全反式维甲酸和三氧化二砷抑制子宫内膜癌细胞生长及其与NDRG1基因的关系[J].临床肿瘤学杂志,2013,18(5):390-393.
作者姓名:陈玲  耿晓星
作者单位:150040 哈尔滨 哈尔滨医科大学附属第三医院妇科
基金项目:黑龙江省教育厅科学技术研究资助项目
摘    要:目的 探讨全反式维甲酸(ATRA)和三氧化二砷(As2O3)对人子宫内膜癌HEC-2B细胞体外生长的抑制作用及其与分化相关基因1(NDRG1)的关系。方法 采用MTT法比较不同浓度(1×10-7、5×10-7、1×10-6、5×10-6和1×10-5mol/L)ATRA和(1.0、2.0、4.0、8.0和16.0μmol/L)As2O3对子宫内膜癌HEC-2B细胞的增殖抑制作用,Western blotting检测HEC-2B细胞中NDRG1蛋白的表达情况。结果 镜下观察,经ATRA和As2O3作用48h后的子宫内膜癌HEC-2B细胞呈现凋亡的特征性改变。1×10-7~1×10-5mol/L 的ATRA和1.0~16.0μmol/L的As2O3能够抑制子宫内膜癌HEC-2B细胞的生长,呈剂量和时间依赖性。ATRA和As2O3能够从蛋白水平调节NDRG1的表达,其表达随药物浓度的增加逐渐下调。结论 ATRA和As2O3能够抑制子宫内膜癌HEC-2B细胞的生长,该抑制作用可能与NDRG1蛋白下调有关。

关 键 词:子宫内膜癌  全反式维甲酸  三氧化二砷  NDRG1  HEC-2B细胞
收稿时间:2013-01-04
修稿时间:2013-03-06

The inhibitory effect of all-trans retinoic acid and arsenic trioxide on the growth of endometrial cancer cells and the relation with NDRG1
CHEN Ling , GENG Xiaoxing.The inhibitory effect of all-trans retinoic acid and arsenic trioxide on the growth of endometrial cancer cells and the relation with NDRG1[J].Chinese Clinical Oncology,2013,18(5):390-393.
Authors:CHEN Ling  GENG Xiaoxing
Institution:Department of Gynecology,the Third Affiliated Hospital to Harbin Medical University,Harbin 150040,China
Abstract:Objective To explore the inhibitory effect of all-traMs retinoic acid(ATRA) and arsenic trioxide( As2O3 ) on the growth of human endometrial cancer HEC-2B cells in vitro and its relation with N-myc downstream regulated genel ( NDRG1 ) protein. Methods Tetrazolium salt assay (MTT) was used to compare the inhibitory effect of different concentration of ATRA ( 1 ×10^-7, 5 ×10^-7, 1 ×10^-6, 5 ×10^-6 and 1 × 10^-5 mol/L) and As2O3(1.0, 2.0, 4.0, 8.0 and 16.01μmol/L) on the growth of HEC-2B cells. The expression of NDRG1 protein was determined by Western blotting analysis. Results After treated with ATRA and As203 for 48h, the HEC-2B cells showed apoptotic change. ATRA 1 × 10^-7-1 ×10^5mol/L and As2O3 1.0-16. 0μmol/L inhibited the cell prolifera- tion in a dose-and time-dependent manner. Western blotting method showed that ATRA and As2O3down-regulated the expression of NDRG1 protein in a dose-dependent manner. Conclusion ATRA and As2O3 can significantly inhibit the growth of human endometrial cancer HEC-2B cells in vitro. The effect may be related to the down-regulation of NDRG1 protein expression.
Keywords:Endometrial cancer  All-traMs retinoic acid  Arsenic trioxide  N-myc downstream regulated gene 1 (NDRGI)  HEC-2B ceils
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