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首页> 外文期刊>Advanced Biomedical Research >Comparison of the anti-cancer effect of Disulfiram and 5-Aza-CdR on pancreatic cancer cell line PANC-1
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Comparison of the anti-cancer effect of Disulfiram and 5-Aza-CdR on pancreatic cancer cell line PANC-1

机译:双硫仑和5-Aza-CdR对胰腺癌细胞株PANC-1的抗癌作用比较

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Background: Pancreatic cancer has poor prognosis by surgical and chemotherapy when it is diagnosed, so other anti-cancerous assistant therapeutic drugs are suggested e.g. epigenetic reversal of tumor-suppressor genes on promoter hypermethylation. 5-Aza-CdR is a nucleoside analog of DNMTi but it has long-term cytotoxicity effects. This study compares the anticancer effect of 5-Aza-CdR and Disulfiram potencies on PANC-1 cell line and up-regulation of p21. Materials and Methods : PANC-1 cell line was cultured in DMEM high glucose and treated by 5-Aza-CdR with 5 and 10 μM concentration for four days and 13 μM DSF (Diulfiram) for 24 hours. MS-PCR and RT-PCR were carried out to detect the methylation pattern and estimate the mRNA expression of RASSF1A and p21 in PANC-1. Result : MS-PCR demonstrated partial unmethylation after treatment with 5-Aza-CdR while there was no unmethylated band after DSF treatment. RT-PCR showed significant differences between re-expression of RASSF1A before and after treatment with 10 μM 5-Aza-CdR ( P P > 0.05). The significant correlation was observed between RASSF1A re-expression and p21 up-regulation before and after treatment with 10 μM 5-Aza-CdR ( P P > 0.05), while p21 up-regulation was significantly higher after DSF treatment ( P Conclusion: Our findings indicated that 5-Aza-CdR induces the re-expression of RASSF1A and p21 up-regulation in PANC-1. DSF showed no epigenetic reversion while it affected p21 up-regulation.
机译:背景:胰腺癌被诊断时通过手术和化学疗法的预后较差,因此建议使用其他抗癌辅助治疗药物,例如启动子高甲基化后肿瘤抑制基因的表观遗传逆转。 5-Aza-CdR是DNMTi的核苷类似物,但具有长期的细胞毒性作用。这项研究比较了5-Aza-CdR和双硫仑效力对PANC-1细胞系和p21上调的抗癌作用。材料和方法:将PANC-1细胞系在高浓度DMEM中培养,并用5-Aza-CdR分别以5和10μM的浓度处理4天,并用13μM的DSF(Diulfiram)处理24小时。进行了MS-PCR和RT-PCR检测甲基化模式并估计了PANC-1中RASSF1A和p21的mRNA表达。结果:MS-PCR显示5-Aza-CdR处理后部分未甲基化,而DSF处理后无未甲基化带。 RT-PCR显示在用10μM5-Aza-CdR治疗前后RASSF1A的重新表达之间存在显着差异(P P> 0.05)。在用10μM5-Aza-CdR治疗前后,RASSF1A表达与p21上调之间存在显着相关性(PP> 0.05),而DSF治疗后p21上调显着更高(P结论:我们的发现提示5-Aza-CdR诱导了PANC-1中RASSF1A的重新表达和p21的上调,DSF没有表观遗传回复,而影响p21的上调。

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