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快速大容量尾静脉注射法建立肝细胞癌小鼠模型
引用本文:秦中强,周万飞,李红俊,刘明珠,谈燚. 快速大容量尾静脉注射法建立肝细胞癌小鼠模型[J]. 蚌埠医学院学报, 2018, 43(11): 1408-1410. DOI: 10.13898/j.cnki.issn.1000-2200.2018.11.003
作者姓名:秦中强  周万飞  李红俊  刘明珠  谈燚
作者单位:1. 蚌埠医学院第一附属医院 肝胆外科, 安徽 蚌埠 233004;2. 蚌埠医学院病理生理学实验室, 安徽 蚌埠 233030
基金项目:安徽省教育厅自然科学研究重点项目
摘    要:目的:通过快速大容量尾静脉注射法建立肝细胞癌小鼠模型。方法:采用快速大容量尾静脉注射法,将插入NRAS基因的NRASV12转座子质粒、表达myr-Akt基因转座子质粒以及转座酶SB100的混合盐溶液通过小鼠尾静脉大容量(2 mL)、短时间(7 s)进行注射,作为观察组;同时设置对照组,同样方法注射等量0.9%氯化钠注射液。注射3~4周后,处死观察组及对照组小鼠,通过病理学检查小鼠成瘤情况。结果:观察组小鼠成瘤率100%(24/24),经病理学检测为肝细胞癌;对照组小鼠无成瘤。结论:快速大容量尾静脉注射方法构建肝细胞癌小鼠模型方法简单,诱癌时间短,成功率高,重复性好。

关 键 词:肝细胞癌   快速大容量尾静脉注射   转座子   小鼠模型
收稿时间:2017-07-03

Establishment of mouse model of hepatocellular carcinoma using rapid and vast tail vein injection
Affiliation:1. Department of Hepatobiliary Surgery, The First Affiliated Hospital of Bengbu Medical College, Bengbu Anhui 233004;2. Laboratory of Pathophysiology, Bengbu Medical College, Anhui Bengbu 233030, China
Abstract:Objective: To establish the mouse model of hepatocellular carcinoma using rapid and vast tail vein injection.Methods: The mixed solution(2 mL) of transposon plasmid NRASV12 inserted by NRAS gene,transposon plasmid expressing activated AKT(myr-Akt) and transposase SB100 was injected into the tail vein of mice within 7 s(observation group).Mouse injected with the same volume saline was set as the control group.After 3 to 4 weeks of injection,the mice of the two groups were sacrificed,and the tumor formation was examined by pathology.Results: The tumor formation rate in observation group was 100%(24/24),and the hepatocellular carcinoma was identified by pathology.No tumor formation in control group was found.Conclusions: Establishment of the mouse model of hepatocellular carcinoma using rapid and vast tail vein injection is simple,has short cancer-inducing time,high success rate and good repeatability.
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