Generation of clonal zebrafish lines and transplantable hepatic tumors

被引:47
作者
Mizgirev, Igor [1 ,2 ]
Revskoy, Sergei [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Hepatol, Chicago, IL 60611 USA
[2] NN Petrov Oncol Res Inst, Lab Genet Toxicol, St Petersburg, Russia
关键词
IN-VIVO; TRANSGENIC ZEBRAFISH; CANCER MODEL; DANIO-RERIO; MELANOMA; ANGIOGENESIS; GENESIS;
D O I
10.1038/nprot.2010.8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transplantable tumors are an accepted gold standard in cancer studies in rodents. The progress of this model in zebrafish has long been constrained by the lack of true inbred lines in zebrafish. We have generated several lines of homozygous diploid clonal zebrafish lines, which allow serial transplantations of tumor cells from one fish to another without sublethal gamma-irradiation. The spectrum of transplantable tumors that were initially induced and maintained in inbred clonal zebrafish lines was limited to different types of spontaneous and diethylnitrosamine-induced hepatic tumors. However, this model can readily be extended to a broad range of extrahepatic tumors, transgenic tumors with defined mechanisms of induction and fluorescence-tagged tumor lines. These models will further facilitate in-depth analysis of invasive tumor growth, angiogenesis, metastasis and tumor-initiating cells by in vivo imaging and provide a cost-effective system for high-throughput (HTP) screening of anticancer therapeutics, including biological response modifiers. In addition, homozygous zebrafish lines are an indispensable tool for immunogenetics, mapping of quantitative trait loci and other genetic applications. The whole procedure, from generation of a gynogenetic female homozygous fish (a founder) to obtaining 3-4 consecutive passages of a syngeneic tumor, takes similar to 12-18 months. This time-frame largely depends on methods of tumor induction, tumor type and tumor growth rate.
引用
收藏
页码:383 / 394
页数:12
相关论文
共 33 条
[11]   Modeling metastasis in vivo [J].
Khanna, C ;
Hunter, K .
CARCINOGENESIS, 2005, 26 (03) :513-523
[12]  
KHUDOLEY VV, 1980, J NATL CANC I MONOGR, V65, P65
[13]   GENETICS AND EARLY DEVELOPMENT OF ZEBRAFISH [J].
KIMMEL, CB .
TRENDS IN GENETICS, 1989, 5 (08) :283-288
[14]   Conservation of gene expression signatures between zebrafish and human liver tumors and tumor progression [J].
Lam, SH ;
Wu, YL ;
Vega, VB ;
Miller, LD ;
Spitsbergen, J ;
Tong, Y ;
Zhan, HQ ;
Govindarajan, KR ;
Lee, S ;
Mathavan, S ;
Murthy, KRK ;
Buhler, DR ;
Liu, ET ;
Gong, ZY .
NATURE BIOTECHNOLOGY, 2006, 24 (01) :73-75
[15]   Effects of RAS on the genesis of embryonal rhabdomyosarcoma [J].
Langenau, David M. ;
Keefe, Matthew D. ;
Storer, Narie Y. ;
Guyon, Jeffrey R. ;
Kutok, Jeffery L. ;
Le, Xiuning ;
Goessling, Wolfram ;
Neuberg, Donna S. ;
Kunkel, Louis M. ;
Zon, Leonard I. .
GENES & DEVELOPMENT, 2007, 21 (11) :1382-1395
[16]   In vivo tracking of T cell development, ablation, and engraftment in transgenic zebrafish [J].
Langenau, DM ;
Ferrando, AA ;
Traver, D ;
Kutok, JL ;
Hezel, JPD ;
Kanki, JP ;
Zon, LI ;
Look, AT ;
Trede, NS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) :7369-7374
[17]   Myc-induced T cell leukemia in transgenic zebrafish [J].
Langenau, DM ;
Traver, D ;
Ferrando, AA ;
Kutok, JL ;
Aster, JC ;
Kanki, JP ;
Lin, S ;
Prochownik, E ;
Trede, NS ;
Zon, LI ;
Look, AT .
SCIENCE, 2003, 299 (5608) :887-890
[18]   Transplantable tumor lines generated in clonal zebrafish [J].
Mizgireuv, IV ;
Revskoy, SY .
CANCER RESEARCH, 2006, 66 (06) :3120-3125
[19]   Carcinogenic effect of N-nitrosodimethylamine on diploid and triploid zebrafish (Danio rerio) [J].
Mizgireuv, IV ;
Majorova, IG ;
Gorodinskaya, VM ;
Khudoley, VV ;
Revskoy, SY .
TOXICOLOGIC PATHOLOGY, 2004, 32 (05) :514-518
[20]   Assessment of polymorphism in zebrafish mapping strains [J].
Nechiporuk, A ;
Finney, JE ;
Keating, MT ;
Johnson, SL .
GENOME RESEARCH, 1999, 9 (12) :1231-1238