细胞培养
癌症
结直肠癌
异种移植
生物
癌变
癌症研究
细胞
移植
癌细胞
病理
医学
内科学
遗传学
作者
Virginie Dangles-Marie,Marc Pocard,Sophie Richon,Louis‐Bastien Weiswald,Franck Assayag,Patrick Saulnier,Jean‐Gabriel Judde,Jean-Louis Janneau,Nathalie Auger,Pierre Validire,Bernard Dutrillaux,Françoise Praz,Dominique Bellet,Marie‐France Poupon
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2007-01-01
卷期号:67 (1): 398-407
被引量:170
标识
DOI:10.1158/0008-5472.can-06-0594
摘要
Abstract Obtaining representative human colon cancer cell lines from fresh tumors is technically difficult. Using 32 tumor fragments from patients with colon cancer, the present study shows that prior xenograft leads to more efficient cell line establishment compared with direct establishment from fresh tumors (P < 0.05). From 26 tumor specimens, we successfully established 20 tumor xenografts in nude mice (77%); among 19 of these xenografts, 9 (47%) led to cell lines, including four from liver metastases. Only 3 of 31 tumor specimens (9.7%) grew immediately in vitro, and all were derived from primary tumors. To compare major phenotypic and genotypic characteristics of human colon cancer cell lines derived from the same tumor fragment using two protocols, the two pairs of cell lines obtained from 2 of 32 tumor fragments were extensively studied. They displayed similar morphology and were able to form compact spheroids. Chemosensitivity to 5-fluorouracil, CPT11, and L-OHP differed between cell lines obtained from patient tumors and those derived from xenografts. Matched cell lines shared a common core of karyotype alterations and distinctive additional chromosomal aberrations. Expression levels of genes selected for their role in oncogenesis evaluated by real-time quantitative PCR were found to be statistically correlated whatever the in vitro culture model used. In conclusion, xenotransplantation in mice of tumor fragments before establishment of cell lines enables generation of more novel human cancer cell lines for investigation of colon cancer cell biology, opening up the opportunity of reproducing the diversity of this disease. [Cancer Res 2007;67(1):398–407]
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