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论文摘要

绿色荧光蛋白转染标记腺样囊性癌生长的裸鼠模型

Establishment of a green fluorescent protein-labeled mouse model of adenoid cystic carcinoma

作者:陈正岗 董作青 张东 周成军 孙善珍 刘少华 魏奉才

Author:Chen Zhenggang1, Dong Zuoqing1, Zhang Dong1, Zhou Chengjun2, Sun Shanzhen3, Liu Shaohua1, Wei Fengcai1

收稿日期:2011-08-25          年卷(期)页码:2011,29(04):424-424-428

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:腺样囊性癌,绿色荧光蛋白,肿瘤模型,动物模型,

Key words:adenoid cystic carcinoma,green fluorescent protein,tumor model,animal model,

基金项目:

国家自然科学基金资助项目(30672339);教育部留学回国人员科研启动基金资助项目(2007)

中文摘要

目的建立能够实时监测、连续动态观察腺样囊性癌生长、转移的裸鼠模型。方法用逆转录病毒载体pLEGFP-N1感染腺样囊性癌细胞系ACCM并筛选出ACCM-GFP稳定细胞株,并比较ACCM和ACCM-GFP细胞的增殖特性和形态特点;用ACCM-GFP细胞种植法建立裸鼠舌癌模型,对移植瘤的生长进行实时荧光成像观察,并与ACCM肿瘤进行组织学比较。结果ACCM-GFP细胞可长期稳定表达GFP;ACCM和ACCM-GFP细胞的增殖特性和形态无差异,体内成瘤的组织学表现无差异;通过活体荧光成像系统可实时监测肿瘤的生长。结论ACCM-GFP裸鼠荧光肿瘤模型可以长期无创、实时、动态观察肿瘤的生长变化,是进行腺样囊性癌基础和临床研究的理想肿瘤模型。

英文摘要

Objective To establish a novel nude mice model which can be visualized in real time and detected in a continuous and dynamic way for the development and metastasis of adenoid cystic carcinoma. Methods Human adenoid cystic carcinoma cells, ACCM cell line, were infected with retroviral vector of pLEGFP-N1 and then screened for a single colony of ACCM-GFP cells. Cell proliferation and morphological analysis were conducted for ACCM and ACCMGFP cells. Nude mice lingual carcinoma model was set up with ACCM-GFP cells injection and real time observation with fluorescence imaging on ACCM-GFP tumors was performed subsequently. Histological assay was analyzed for ACCM and ACCM-GFP tumors as well. Results ACCM-GFP cells were able to express GFP stably in the long term. ACCM and ACCM-GFP cells showed no significant difference in cell proliferation and morphology, and no significant difference of histological characteristics in vivo could be found between ACCM and ACCM-GFP tumors. Tumor development could be monitored in real time with fluorescence imaging system in vivo. Conclusion GFP-expressing ACCM tumor model can be applied to detect and observe its development in the long term in a noninvasive, real time and dynamic way. It is also a kind of ideal in vivo mouse model for adenoid cystic carcinoma research.

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