首页 | 本学科首页   官方微博 | 高级检索  
     

大鼠胰腺癌细胞系R-PC的建立及其生物学特性
引用本文:夏维,秦仁义. 大鼠胰腺癌细胞系R-PC的建立及其生物学特性[J]. 中华实验外科杂志, 2006, 23(6): 692-694
作者姓名:夏维  秦仁义
作者单位:430030,武汉,华中科技大学同济医学院附属同济医院普外科
摘    要:目的 建立1株大鼠源胰腺癌细胞系R-PC。方法 利用胰腺包膜下埋二甲基苯并蒽(DMBA)致癌药物的方法建立大鼠胰腺癌模型,用组织块法和胶原酶消化法进行原代培养,观察细胞形态学特征,研究细胞生长状态,测定细胞周期,计数染色体数目。组织化学染色和异种移植。结果 经过11个月的体外培养,连续传代80余次;细胞生长迅速,倍增时间为34h;染色体数目在42-76之间。免疫组织化学染色显示细胞角蛋白、细胞角蛋白19和细胞角蛋白20阳性;异种移植成瘤率为100%。结论 R-PC是高度恶性的大鼠胰腺癌细胞系,为体内和体外研究恶性细胞的增值和发展提供了优秀工具。

关 键 词:胰腺癌 细胞培养 生物学
收稿时间:2005-09-26
修稿时间:2005-09-26

Establishment and biological characteristics of a rat pancreatic cancer cell line
XIA Wei,QIN Ren-yi. Establishment and biological characteristics of a rat pancreatic cancer cell line[J]. Chinese Journal of Experimental Surgery, 2006, 23(6): 692-694
Authors:XIA Wei  QIN Ren-yi
Affiliation:Department of General Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of .Science and Technology, Wuhan 430030, China
Abstract:Objective To establish a rat pancreatic cancer cell line R-PC. Methods A new pancreatic cancer cell line was established from pancreatic cancer in the rat induced by DMBA. The cells were cultured by explant culture and enzymatic digestion. Serially passaged cells were characterized by morphology, cytogenetics, immunocytochemistry analysis and xenografts into nude mouse. Results The new pancreatic carcinoma cell line was established from rat pancreatic adenocarcinoma. The cell line has been maintained for over 80 passages during 11 months. Cells grew rapidly, with a doubling time of 34 h. Chromosome number ranged from 42 to 76. The histochemical staining of keratin, cytokeratin 19 and cytokeratin 20 were all positive, and the ratio of heterotransplantation was 100%. Conclusion R-PC was demonstrated as a high malignant rat pancreatic cancer cell line and can be a useful model to study the malignant cell proliferation and differentiation in both in vivo and in vitro.
Keywords:Pancreatic carcinoma   Cell culture   Biology
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号