Establishment and Characterization of Two Novel Cholangiocarcinoma Cell Lines

被引:7
|
作者
Zhang, Yanhua [1 ]
Luo, Jingfeng [2 ]
Dong, Xue [2 ]
Yang, Fang [1 ]
Zhang, Miaofeng [3 ]
Zhao, Juanjuan [4 ]
Wang, Qiangfeng [5 ]
Zhou, Fei [2 ]
Sun, Jihong [2 ]
Yang, Xiaoming [2 ,6 ]
机构
[1] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Dept Radiol, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Orthopaed, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Dept Cardiol,Biomed Res Therapy Ctr, Hangzhou, Zhejiang, Peoples R China
[5] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Oncol, Hangzhou, Zhejiang, Peoples R China
[6] Univ Washington, Sch Med, Dept Radiol, Image Guided Biomol Intervent Res, Seattle, WA 98195 USA
基金
中国国家自然科学基金;
关键词
BILIARY-TRACT; CONTAMINATION; EXPRESSION; DIAGNOSIS; RECEPTOR; LIVER; TP53;
D O I
10.1245/s10434-019-07649-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Cholangiocarcinoma (CCA) is a rare, aggressive and highly lethal tumor. The disease is very difficult to diagnose and multi-modality treatments are ineffective. To improve our understanding of the biological characteristics of CCA, and facilitate the identification of valid treatments, an in-depth characterization of two novel Chinese patient-derived primary CCA cell lines was performed. Methods. Two CCA cell lines were developed and labelled ZJU-0826 and -1125. The two cell lines were characterized with respect to phenotypic, molecular, biomarker, functional and histological properties. Results. Two novel cell lines were cultured for 2 years, and maintained for more than 100 passages. They retained their typical biliary epithelial morphology and ultrastructure. The population doubling times of ZJU-0826, and -1125 were 63.84 h and 44.73 h, respectively. The cells exhibited near-triploid karyotypes with complex structural aberrations. ZJU-1125 cells had mutations in TP53 exons. Short tandem repeats genotyping confirmed the human origin and difference between lines. An immunophenotype analysis showed that ZJU-0826 is positive for CD44, CD29, Pdx1, CD236, FoxA1, FoxA2, and Nanog, and ZJU-1125 positive for CD44, CD29, CD133, Pdx1, FoxA1, FoxA2, and Nanog. ZJU-1125 had greater invasion ability in vitro and tumorigenicity than those of ZJU-0826. Conclusions. Our results confirm the validity of the ZJU-0826 and -1125 as representative models for the elucidation of the molecular pathogenesis of perihilar CCA, and intrahepatic CCA in both in vitro and in vivo studies, respectively.
引用
收藏
页码:4134 / 4147
页数:14
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