Establishment in severe combined immunodeficiency mice of subrenal capsule xenografts and transplantable tumor lines from a variety of primary human lung cancers: Potential models for studying tumor progression-related changes

被引:80
作者
Cutz, Jean-Claude
Guan, Jun
Bayani, Jane
Yoshimoto, Maisa
Xue, Hui
Sutcliffe, Margaret
English, John
Flint, Julia
LeRiche, Jean
Yee, John
Squire, JeremyA.
Gout, Peter W.
Lam, Stephen
Wang, Yu-Zhuo
机构
[1] British Columbia Canc Agcy, Res Ctr, Dept Canc Endocrinol, Vancouver, BC V5Z 1L3, Canada
[2] British Columbia Canc Agcy, Dept Canc Imaging, Vancouver, BC V5Z 1L3, Canada
[3] Vancouver Gen Hosp, Dept Pathol, Vancouver, BC V5Z 1M9, Canada
[4] Vancouver Gen Hosp, Dept Surg, Vancouver, BC V5Z 1M9, Canada
[5] Univ Hlth Network, Ontario Canc Inst, Dept Appl Mol Oncol, Vancouver, BC, Canada
[6] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[7] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
关键词
D O I
10.1158/1078-0432.CCR-06-0252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Lung cancer is a biologically diverse disease and relevant models reflecting its diversity would facilitate the improvement of existing therapies. With a view to establishing such models, we developed and evaluated xenografts of a variety of human lung cancers. Experimental Design: Using nonobese diabetic/severe combined immunodeficiency mice, subrenal capsule xenografts were generated from primary lung cancer tissue, including moderately and poorly differentiated squamous cell carcinoma, adenocarcinoma, adenosquamous carcinoma, small cell carcinoma, large cell undifferentiated carcinoma, and carcinosarcoma. After 4 to 12 weeks, xenografts were harvested for serial transplantation and comparison with the original tissue via histologic, chromosomal, and cytogenetic analyses. Results: Xenografts were successfully established. H&E staining showed that xenografts retained major histologic features of the original cancers. Immunohistochemistry and fluorescence in situ hybridization confirmed the human origin of the tumor cells and development in xenografts of murine supportive stroma. Four transplantable lines were developed from rapidly growing tumors (>5 generations), i.e., a small cell lung carcinoma, large cell undifferentiated carcinoma, pulmonary carcinosarcoma, and squamous cell carcinoma. Analyses including spectral karyotyping, comparative genomic hybridization, and fluorescence in situ hybridization, revealed that the xenografts were genetically similar to the original tumors, showing chromosomal abnormalities consistent with karyotypic changes reported for lung cancer. Conclusions: The subrenal capsule xenograft approach essentially provides a living tumor bank derived from patient material and a means for isolating and expanding specific cell populations. The transplantable tumor lines seem to provide good models for studying various aspects of tumor progression and a platform for developing novel therapeutic regimens, with the possibility of patient-tailored therapies.
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页码:4043 / 4054
页数:12
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