DEN诱发PLCε基因敲除小鼠肝癌模型的建立
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Establishment of DEN Induced PLCε Knock-out Mouse Liver cancer Model
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    摘要:

    目的 通过突变诱发剂二乙基亚硝胺(diethylnitrosamine DEN)联合肿瘤增强剂苯巴比妥(phenobarbital PB)诱发PLCε基因敲除小鼠建立肝脏肿瘤动物模型。方法 随机选取出生12日龄的雄性PLCε-/-小鼠和PLCε+/+小鼠各40只(分别为实验组Ⅰ、实验组Ⅱ),先腹腔注射DEN,4周龄后开始加饮PB药水,持续喂养;同样随机选取出生12日龄的雄性PLCε-/-小鼠和PLCε+/+小鼠各40只(分别为对照组Ⅰ、对照组Ⅱ)正常喂养;实验周期均为24周,实验结束后在电子显微镜下观察小鼠肝脏肿瘤的形成。 结果 经病理学结果证实,实验组Ⅱ小鼠发生肝脏肿瘤18只,成癌率为60%,实验组Ⅰ小鼠发生肝脏肿瘤15只,成癌率为46.9%。而对照组Ⅰ、Ⅱ的小鼠均未发生肝癌。结论 以上研究结果表明,成功建立了PLCε基因敲除小鼠肝脏肿瘤模型,为进一步研究PLCε基因在肝脏肿瘤形成中发生机制奠定了基础。

    Abstract:

    To establish animal models of liver tumors, the PLCε gene knockout mice was induced by mutation inducers Diethylnitrosamine (diethylnitrosamine DEN) combined with tumor enhancer phenobarbital (phenobarbital PB). Methods 12-day-old male PLCε-/ - and PLCε + / + mice were randomly selected as group I (n= 40)and group II (n= 40),respectively.The mice of group I and II were injected DEN through abdominal cavity at the age of 12 days,then drinking PB after 4 weeks and continuously until 24 weeks. At the same time, 12-day-old male PLCε-/ - and PLCε + / + mice were randomly selected as the control group I (n= 40) and control group II (n= 40), respectively, and fed with normal feeds for 24 weeks. At the end of the experiment, the liver tumor was observed under electron microscopy. Results Pathology results confirm that 18 mice of group II had liver tumors, and rate of tumor formation is 60%; 15 mice of group I had liver tumors, and rate of tumor formation is 46.9%; the mice of control group I and II had not liver tumors. Conclusions The animal model of liver tumor have been successfully established by using mutation inducers DEN combined with PB in PLCε gene knockout mice, and could provide a foundation for further researching effects of PLCε during liver tumor formation.

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李瑞生. DEN诱发PLCε基因敲除小鼠肝癌模型的建立[J].中国比较医学杂志,2013,23(3).

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  • 收稿日期:2013-01-07
  • 最后修改日期:2013-02-18
  • 录用日期:2013-02-20
  • 在线发布日期: 2013-03-21
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