于丽波,孙文洲,毕玉美.siRNA干扰Id1表达增强卵巢癌细胞对顺铂的敏感性[J].中国肿瘤,2014,23(9):775-778. |
siRNA干扰Id1表达增强卵巢癌细胞对顺铂的敏感性 |
siRNA Targeting Id1 Enhances Chemosensitivity of Ovarian Cancer Cells to Cisplatin |
投稿时间:2013-12-18 |
DOI:10.11735/j.issn.1004-0242.2014.09.A015 |
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中文关键词: 结合抑制因子 卵巢癌 化疗耐药 |
英文关键词:inhibitor of DNA bindingor differentiation ovarian cancer chemoresistance |
基金项目:黑龙江省教育厅科学技术研究项目(12531275) |
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中文摘要: |
摘 要:[目的] 探讨体外DNA结合抑制因子(inhibitor of DNA bindingor differentiation,Id)的表达对卵巢上皮癌SKOV3对顺铂化疗敏感性的影响。[方法] 构建靶向Id1基因siRNA慢病毒载体并转染SKOV3细胞,筛选出稳定转染的SKOV3细胞克隆。实验分为4组:实验组(Cell+Lv-shRNA-Id1)、阴性对照组(Cell+Lv-shRNA-NC)、病毒对照组(Cell+Lv-control)与空白对照组(Cell group)。CCK8检测各组SKOV3细胞不同时间增殖活性以及暴露于不同浓度顺铂(0.1、0.2、0.5、1、2、5、10μg/ml) 48h后顺铂对各组SKOV3细胞的半数抑制浓度,分析沉默Id1基因后卵巢癌细胞对顺铂化疗敏感性的影响。[结果] 三组对照组细胞增殖活性随着时间增加显著,而实验组则增加缓慢。在48h和72h时,实验组细胞增殖活性值分别为0.449±0.072μg/ml、0.885±0.232μg/ml,与三组对照组比较差异均有统计学意义(P均<0.05);实验组顺铂对SKOV3细胞的半数抑制浓度为1.5±0.71μg/ml,明显低于对照组(P<0.01)。[结论] 抑制Id1基因表达可以增加顺铂对卵巢癌细胞的生长抑制作用,为临床进一步提高卵巢癌的疗效提供了研究基础。 |
英文摘要: |
Abstract:[Purpose] To investigate the effect of inhibitor of DNA binding or differentiation 1(Id1) on the chemosensitivity of ovarian epithelial carcinoma SKOV3 cells to cisplatin in vitro.[Methods] The lentiviral vector of siRNA targeting Id1 gene was constructed and transfected into SKOV3 cells,stably transfected SKOV3 cell was selected and cloned. The experiment was divided into four groups:Cell+Lv-shRNA-ID1、Cell+Lv-shRNA-NC、Cell+Lv-control and Blank cell group. The proliferations of SKOV3 cells at different times were detected by CCK8. SKOV3 cells were exposed to different concentrations of cisplatin(0.1、0.2、0.5、1、2、5、10μg/ml) for 48 hours in each group and half inhibitory concentrations of cisplatin to SKOV3 cells were detected by CCK8 . The effect of targeting Id1 gene on the chemosensitivity in ovarian cancer cells to cisplatin was analyzed. [Results] Cell proliferations in three control groups increased significantly over time,cell proliferations in the Cell+Lv-shRNA-ID1 group increased slowly. Cell proliferations were 0.449±0.072μg/ml at 48h and 0.885±0.232μg/ml at 72h in the Cell+Lv-shRNA-ID1 group,the differences were statistically significant compared with three control groups(P all <0.05). Half inhibitory concentration of cisplatin to SKOV3 cells in the Cell+Lv-shRNA-ID1 group was 1.5±0.71μg/ml which was significantly lower than that in three control groups(P<0.01) with no significant difference among the three control groups. [Conclusion] Silence of Id1 expression increases growth inhibition effect of cisplatin to ovarian cancer cells. It provides the research foundation for further improving the clinical efficacy for ovarian cancer. |
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