中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2014年
9期
791-793
,共3页
王丽红%张志华%朱松岩%赵蕾%郝长来
王麗紅%張誌華%硃鬆巖%趙蕾%郝長來
왕려홍%장지화%주송암%조뢰%학장래
丙戊酸钠%细胞周期%细胞周期蛋白%细胞周期蛋白依赖性激酶
丙戊痠鈉%細胞週期%細胞週期蛋白%細胞週期蛋白依賴性激酶
병무산납%세포주기%세포주기단백%세포주기단백의뢰성격매
valproic acid%cell cycle%cyclin%cyclin-dependent kinase
目的:检测丙戊酸钠( VPA)在动物体内对白血病细胞周期蛋白( cyclins )及细胞周期蛋白依赖性激酶( CDKs)表达的影响。方法建立急性髓系白血病Kasumi-1细胞裸鼠移植瘤模型,分为对照组及VPA治疗组(腹腔注射VPA 500 mg· kg-1,2周),用RT-PCR法检测cyclinD1、cyclinE1和CDK4、CDK6、CDK2的mRNA的表达水平,用Western blot法检测cyclinD1蛋白的表达水平。结果与对照组相比,VPA治疗组cyclinD1、cyclinE1和CDK4、CDK6、CDK2 mRNA的表达明显下调( P<0.05);cyclinD1蛋白的表达明显下降( P<0.01)。结论 VPA下调cyclinD1、cyclinE1、CDK4、CDK6和CDK2的表达,是VPA诱导肿瘤细胞周期阻滞的机制之一。
目的:檢測丙戊痠鈉( VPA)在動物體內對白血病細胞週期蛋白( cyclins )及細胞週期蛋白依賴性激酶( CDKs)錶達的影響。方法建立急性髓繫白血病Kasumi-1細胞裸鼠移植瘤模型,分為對照組及VPA治療組(腹腔註射VPA 500 mg· kg-1,2週),用RT-PCR法檢測cyclinD1、cyclinE1和CDK4、CDK6、CDK2的mRNA的錶達水平,用Western blot法檢測cyclinD1蛋白的錶達水平。結果與對照組相比,VPA治療組cyclinD1、cyclinE1和CDK4、CDK6、CDK2 mRNA的錶達明顯下調( P<0.05);cyclinD1蛋白的錶達明顯下降( P<0.01)。結論 VPA下調cyclinD1、cyclinE1、CDK4、CDK6和CDK2的錶達,是VPA誘導腫瘤細胞週期阻滯的機製之一。
목적:검측병무산납( VPA)재동물체내대백혈병세포주기단백( cyclins )급세포주기단백의뢰성격매( CDKs)표체적영향。방법건립급성수계백혈병Kasumi-1세포라서이식류모형,분위대조조급VPA치료조(복강주사VPA 500 mg· kg-1,2주),용RT-PCR법검측cyclinD1、cyclinE1화CDK4、CDK6、CDK2적mRNA적표체수평,용Western blot법검측cyclinD1단백적표체수평。결과여대조조상비,VPA치료조cyclinD1、cyclinE1화CDK4、CDK6、CDK2 mRNA적표체명현하조( P<0.05);cyclinD1단백적표체명현하강( P<0.01)。결론 VPA하조cyclinD1、cyclinE1、CDK4、CDK6화CDK2적표체,시VPA유도종류세포주기조체적궤제지일。
Objective To explore the molecular mechanism of valproic acid ( VPA) inducing tumor cell cycle arrest , by determining the expres-sion of cyclins and cyclin -dependent kinases ( CDKs).Methods Nude mice model with xenograft Kasumi -1 tumor was established by subcuta-neous inoculation of Kasumi -1 cells, and devided two groups: control group and VPA treatment group ( intraperitoneal injection of VPA 500 mg· kg-1 for 2 weeks).The expression levels of cyclinD1, cyclinE1, CDK4, CDK6, CDK2 mRNA were determined by semi -quantitative RT-PCR.The expression level of cyclinD 1 protein was determined by Western blot.Results Compared with the control group , VPA signifi-cantly reducted the expression of cyclinD 1, cyclinE1, CDK4, CDK6, CDK2 mRNA( P<0.05 );and reduced the expression of cyclinD 1 protein ( P<0.01 ).Conclusion The mechanism that VPA inductes cell cycle arrest is possibly due to downregulation of cyclin D 1, CDK4/6, cyclin E and CDK2 expression.