反义寡核苷酸抑制大鼠胶质瘤多药耐药细胞株中Pgp相关基因表达的实验研究  

Experimental study of inhibiting process of gene expression of Pgp in multidrug resistant rat glioma cell line (C6/adr) by antisense oligodeoxynucleotides

在线阅读下载全文

作  者:张健[1] 张庆林[1] 王成伟[1] 孔建新[1] 郭华[1] 刘福生[1] 陶荣杰[1] 马道新[1] 

机构地区:[1]山东大学第二医院神经外科,济南250033

出  处:《中华神经外科杂志》2004年第5期353-356,共4页Chinese Journal of Neurosurgery

基  金:国家自然科学基金资助(30070272)

摘  要:目的通过研究反义寡核苷酸对大鼠胶质瘤多药耐药细胞株C6/adr中Pgp相关基因表达的抑制作用,探讨寡核苷酸在细胞内的代谢过程.方法根据MDR-1基因序列合成反义寡核苷酸转染胶质瘤耐药细胞,应用RT-PCR、流式细胞仪等方法,分别在转染后6、12、24、48h对其进行MDR-1mRNA水平及Pgp含量的检测.结果流式细胞及RT-PCR结果显示转染后6h即可发现胶质瘤耐药细胞Pgp和MDR-1 mRNA减低,减低程度与转染后的检测时间相关,12~24h减低程度最为显著(P<0.05),48h后恢复至转染前的水平.结论反义寡核苷酸抑制大鼠胶质瘤细胞的PgP表达和减低MDR-1 mRNA水平具有明显的细胞内的代谢过程,了解其作用的规律性有助于选择适宜的用药时机,更大限度地提高疗效.Objective To explore the inhibiting process of gene expression of Pgp and metabolism of antisense oligodeoxynucleotides in multidrug resistant rat glioma cell line (C6/adr). Methods The antisense phosphorothioate-modified ODNs were designed to target MDR-1 gene and the ODNs were delivered by a cationic lipid vector to the rat glioma cells. The level of P-glycoprotein expression and MDR-1 mRNA of the treated glioma cells were detected by FCM and RT-PCR at the point of 6,12,24 and 48 hours after transfection. Results The outcome of FCM and RT-PCR showed that the glioma cells treated with antisense ODNs came into a decreased level of P-glycoprotein expression and MDR-1 mRNA,which began at 6 hours after transfection and came to a peak during 12 to 24 hours(P<0.05),and the level of pre-transfection was recovered after 48 hours. Conclusion There is an obviously inhibiting process of P-glycoprotein expression and the level of MDR-1 mRNA in rat glioma cells by antisense ODNs. Consequently, the proper time of chemical therapy can be chosen according to the rule of the antisense oligodeoxynucleotides metabolism .

关 键 词:胶质瘤 反义寡核苷酸 转染 大鼠 多药耐药细胞株 MDR-1 相关基因表达 结论 适宜 水平 

分 类 号:R73-3[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象