Transplantable Tumor Lines Generated in Clonal Zebrafish
Open Access
- 15 March 2006
- journal article
- Published by American Association for Cancer Research (AACR) in Cancer Research
- Vol. 66 (6) , 3120-3125
- https://doi.org/10.1158/0008-5472.can-05-3800
Abstract
Transplantable zebrafish tumors are a novel and very promising model in cancer research. However, further progress in this field has been contained by a lack of true inbred lines in zebrafish. To overcome this problem, we generated two lines of homozygous diploid clonal zebrafish lines (i.e., CB1 and CW1), which allowed us to carry out transplantation of any tissue, including tumors, from one fish to another within a line without rejection of the graft. The primary tumors in CB1 fish were induced by N-nitrosodiethylamine (DEN). The histologic analysis of these tumors revealed different types of hepatocellular carcinomas, hepatoblastomas, hepatoma, cholangiocarcinoma, and pancreatic carcinoma. Four spontaneous acinar cell carcinomas of pancreas were also found in 10- to 18-month-old CB1 fish. Small pieces of tissue or cell suspensions of either DEN-induced or spontaneous tumors were serially transplanted into the peritoneal cavity of syngeneic fish at different stages of development from 5-day-old larvae to adult fish. The development of grossly visible tumors occurred from 2 weeks to 3 months after tumor grafting and grew either as solitary smooth nodules or as an amorphous jelly-like mass infiltrating abdominal organs. The majority of tumors were also successfully transplanted to isogeneic (F1 generation from crossing CB1 × CW1) fish. At the present time, 19 transplantable zebrafish tumor lines have been generated and maintained for as long as 3 to 25 passages. This model provides a novel tool for studying experimental tumor biology and therapy and will become a cost effective system for high throughput screening of anticancer drugs. (Cancer Res 2006; 66(6): 3120-5)Keywords
This publication has 28 references indexed in Scilit:
- A zebrafish bmyb mutation causes genome instability and increased cancer susceptibilityProceedings of the National Academy of Sciences, 2005
- Advances in imaging mouse tumour models in vivoThe Journal of Pathology, 2005
- In vivo drug discovery in the zebrafishNature Reviews Drug Discovery, 2005
- Targeted Expression of Human MYCN Selectively Causes Pancreatic Neuroendocrine Tumors in Transgenic ZebrafishCancer Research, 2004
- The ‘definitive’ (and ‘primitive’) guide to zebrafish hematopoiesisOncogene, 2004
- Carcinogenic Effect of N-Nitrosodimethylamine on Diploid and Triploid Zebrafish (Danio rerio)Toxicologic Pathology, 2004
- Many Ribosomal Protein Genes Are Cancer Genes in ZebrafishPLoS Biology, 2004
- Myc-Induced T Cell Leukemia in Transgenic ZebrafishScience, 2003
- Neoplasia in Zebrafish (Danio rerio) Treated with 7,12-Diniethylbenz[a]anthracene by Two Exposure Routes at Different Developmental StagesToxicologic Pathology, 2000
- Neoplasia in Zebrafish (Danio rerio) Treated with N-methyl-N'nitro-N-nitrosoguanidine by Three Exposure Routes at ifferent Developmental StagesToxicologic Pathology, 2000