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首页> 外文期刊>Annals of the New York Academy of Sciences >Alterations in mRNA Expression of Apoptosis-Related Genes BCL2, BAX, FAS, Caspase-3, and the Novel Member BCL2L12 after Treatment of Human Leukemic Cell Line HL60 with the Antineoplastic Agent Etoposide
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Alterations in mRNA Expression of Apoptosis-Related Genes BCL2, BAX, FAS, Caspase-3, and the Novel Member BCL2L12 after Treatment of Human Leukemic Cell Line HL60 with the Antineoplastic Agent Etoposide

机译:抗肿瘤药依托泊苷处理人白血病细胞系HL60后,凋亡相关基因BCL2,BAX,FAS,Caspase-3和新型成员BCL2L12 mRNA表达的变化

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摘要

Apoptotic cell death is a highly regulated process, which plays a crucial role in many biological events. Etoposide is an antineoplastic drug, which targets the DNA unwinding enzyme, topoisomerase II. The aim of the present research approach to investigate the expression of the apoptosis-related genes BCL2 (Bcl-2), FAS, Caspase-3, BAX and the new member BCL2L12, cloned by our group, along with treatment of HL-60 leukemia cells with etoposide. The kinetics of apoptosis induction and cell toxicity was evaluated by DNA laddering and MTT method, respectively. The mRNA expression levels of the genes were analyzed by RT-PCR using gene-specific primers. β-Actin was used as a control gene. An important downregulation of BCL2L12 was observed at 4 h of drug treatment, whereas BAX was upregulated at the same time point. No alteration in the expression pattern of the other apoptosis-related genes was detected. Since, the main anticarcinogenic effect of etoposide is due to the induction of apoptosis, these changes observed in the mRNA expression levels of the genes may be an underlying mechanism.
机译:凋亡细胞死亡是一个高度调控的过程,在许多生物学事件中起着至关重要的作用。依托泊苷是一种抗肿瘤药,其靶向DNA解旋酶拓扑异构酶II。本研究方法旨在研究由我们小组克隆的凋亡相关基因BCL2(Bcl-2),FAS,Caspase-3,BAX和新成员BCL2L12的表达以及HL-60白血病的治疗方法细胞与依托泊苷。分别通过DNA梯形图和MTT方法评估凋亡诱导的动力学和细胞毒性。使用基因特异性引物通过RT-PCR分析基因的mRNA表达水平。 β-肌动蛋白用作对照基因。在药物治疗4小时后,BCL2L12明显下调,而在同一时间BAX上调。未检测到其他凋亡相关基因的表达模式改变。由于依托泊苷的主要抗癌作用是由于诱导细胞凋亡,因此在基因的mRNA表达水平中观察到的这些变化可能是潜在的机制。

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