Renal carcinogenesis: Genotype, phenotype and dramatype

被引:23
作者
Hino, O [1 ]
Kobayashi, T [1 ]
Momose, S [1 ]
Kikuchi, Y [1 ]
Adachi, H [1 ]
Okimoto, K [1 ]
机构
[1] Japanese Fdn Canc Res, Inst Canc, Dept Expt Pathol, Toshima Ku, Tokyo 1708455, Japan
关键词
D O I
10.1111/j.1349-7006.2003.tb01410.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is a heritable disorder of somatic cells. Environment and heredity are both important in the carcinogenic process. The Eker rat model of hereditary renal carcinoma (RC) is an example of a Mendelian dominantly inherited predisposition to a specific cancer in an experimental animal. Forty years after the discovery of the Eker rat in Oslo, we and Knudson's group independently identified a germline retrotransposon insertion in the rat homologue of the human tuberous sclerosis (TSC2) gene. To our knowledge, this was the first isolation of a Mendelian dominantly predisposing cancer gene in a naturally occurring animal model. Recently, we discovered a new hereditary renal carcinoma in the rat. This rat was named the "Nihon" rat and its predisposing (Nihon) gene could be a novel renal tumor suppressor gene. This article will review the utility of these unique models for the study of problems in carcinogenesis; e.g., species-specific differences in tumorigenesis, cell stage and tissue/cell-type specific tumorigenesis, multistep carcinogenesis, modifier gene(s) in renal carcinogenesis, cancer prevention and the development of therapeutic treatments which can be translated to human patients, as well as how environmental factors interact with cancer susceptibility gene(s). (Cancer Sci 2003; 94: 142-147).
引用
收藏
页码:142 / 147
页数:6
相关论文
共 59 条
[1]   Unique features of dendritic cells in IFN-γ transgenic mice:: Relevance to cancer development and therapeutic implications [J].
Akbar, SMF ;
Kajino, K ;
Tanimoto, K ;
Yamamura, E ;
Onji, M ;
Hino, O .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 259 (02) :294-299
[2]   The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitination [J].
Benvenuto, G ;
Li, SW ;
Brown, SJ ;
Braverman, R ;
Vass, WC ;
Cheadle, JP ;
Halley, DJJ ;
Sampson, JR ;
Wienecke, R ;
DeClue, JE .
ONCOGENE, 2000, 19 (54) :6306-6316
[3]   A DOMINANT GENE FOR RENAL ADENOMAS IN RAT [J].
EKER, R ;
MOSSIGE, J .
NATURE, 1961, 189 (476) :858-+
[4]   HEREDITARY RENAL-CELL CARCINOMA IN THE EKER RAT - A RODENT FAMILIAL CANCER SYNDROME [J].
EVERITT, JI ;
GOLDSWORTHY, TL ;
WOLF, DC ;
WALKER, CL .
JOURNAL OF UROLOGY, 1992, 148 (06) :1932-1936
[5]   Generation of metastatic variants of Eker renal carcinoma cell lines for experimental investigation of renal cancer metastasis [J].
Fukuda, T ;
Hirayama, Y ;
Mitani, H ;
Maeda, H ;
Tsutsumi, M ;
Konishi, Y ;
Hino, O .
JAPANESE JOURNAL OF CANCER RESEARCH, 1998, 89 (11) :1104-1108
[6]  
Fukuda T, 1998, INT J ONCOL, V13, P957
[7]   Tsc tumour suppressor proteins antagonize amino-acid-TOR signalling [J].
Gao, XS ;
Zhang, Y ;
Arrazola, P ;
Hino, O ;
Kobayashi, T ;
Yeung, RS ;
Ru, BG ;
Pan, DJ .
NATURE CELL BIOLOGY, 2002, 4 (09) :699-704
[8]   TSC1 and TSC2 tumor suppressors antagonize insulin signaling in cell growth [J].
Gao, XS ;
Pan, DJ .
GENES & DEVELOPMENT, 2001, 15 (11) :1383-1392
[9]   SPONTANEOUS AND RADIATION-INDUCED RENAL TUMORS IN THE EKER RAT MODEL OF DOMINANTLY INHERITED CANCER [J].
HINO, O ;
KLEINSZANTO, AJP ;
FREED, JJ ;
TESTA, JR ;
BROWN, DQ ;
VILENSKY, M ;
YEUNG, RS ;
TARTOF, KD ;
KNUDSON, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :327-331
[10]   A NOVEL RENAL-CELL CARCINOMA SUSCEPTIBILITY GENE MAPS ON CHROMOSOME-10 IN THE EKER RAT [J].
HINO, O ;
MITANI, H ;
NISHIZAWA, M ;
KATSUYAMA, H ;
KOBAYASHI, E ;
HIRAYAMA, Y .
JAPANESE JOURNAL OF CANCER RESEARCH, 1993, 84 (11) :1106-1109