Xin Bo, Cui Ying, Wang Yanxia, Wang Lei, Yin Jipeng, Zhang Licheng, Pang Hailin, Zhang Helong, Wang Rui-An
Department of Oncology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.
Department of Oncology, No. 88 Hospital of People's Liberation Army, Tai'an, Shandong 271000, P.R. China.
Oncol Lett. 2017 Oct;14(4):4722-4728. doi: 10.3892/ol.2017.6800. Epub 2017 Aug 23.
Liver cancer is the one of most common types of cancer and the 2nd cause of cancer-associated mortalities worldwide. Establishing appropriate animal models of liver cancer is essential for basic and translational studies. The present study evaluated the effects of the combined use of alcohol with a conventional chemical-induced mouse liver cancer model. The treatment of alcohol/diethylnitrosamine (DEN)/carbon tetrachloride (CCl) in the mice of experimental groups resulted in a series of pathological changes in the liver. Liver inflammation, fibrosis, cirrhosis and hepatocellular carcinoma were identified, and this method used less time (1-5 months) for inducement compared with the conventional chemical-induced method alone. In addition, murine α-fetoprotein (mAFP) was expressed throughout and ultrastructural features met the criteria for liver cancer. Fatty degeneration of pancreas, reduced blood glucose levels, and increased spleen weight were observed. These results indicated that an AFP-secreting hepatocellular carcinoma model of BALB/c mouse was successfully developed. The disease process and morphological changes met the criterion of the liver cancer process. Therefore the model developed in the present study may be an ideal animal model for studying the occurrence and development of liver cancer.
肝癌是最常见的癌症类型之一,也是全球癌症相关死亡的第二大原因。建立合适的肝癌动物模型对于基础研究和转化研究至关重要。本研究评估了酒精与传统化学诱导小鼠肝癌模型联合使用的效果。实验组小鼠接受酒精/二乙基亚硝胺(DEN)/四氯化碳(CCl)处理后,肝脏出现了一系列病理变化。鉴定出肝脏炎症、纤维化、肝硬化和肝细胞癌,并且与单独使用传统化学诱导方法相比,该方法诱导所需时间更短(1 - 5个月)。此外,小鼠甲胎蛋白(mAFP)全程表达,超微结构特征符合肝癌标准。观察到胰腺脂肪变性、血糖水平降低和脾脏重量增加。这些结果表明成功建立了BALB/c小鼠分泌AFP的肝细胞癌模型。疾病过程和形态变化符合肝癌进程的标准。因此,本研究建立的模型可能是研究肝癌发生发展的理想动物模型。