The US National Toxicology Program evaluation of transgenic mice as predictive models for identifying carcinogens

被引:26
作者
Eastin, WC [1 ]
机构
[1] NIEHS, Expt Toxicol Branch, Res Triangle Pk, NC 27709 USA
关键词
transgenic; Tg.AC; p53(+/-); NTP; model; carcinogen;
D O I
10.2307/3433914
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
National institute of Environmental Health Sciences researchers have invested considerable effort in exploring the utility of transgenic mice to detect carcinogens and study mechanisms of carcinogenesis. Work has assessed several mouse models genetically altered to enhance their expression of chemically induced tumors. Results with the p53(def) (hemizygous for the tumor-suppressor gene) and the Tg.AC (carrier of an activated H-ras oncogene) mice have been used as a basis for a proposed new strategy for identifying chemical carcinogens and assessing risk. The U.S. National Toxicology Program is conducting a series of studies with these two transgenic strains to further examine their strengths and weaknesses for identification of documented rodent and human carcinogens and to explore their ability to provide information concerning the effective dosimetry for target organ mutation.
引用
收藏
页码:81 / 84
页数:4
相关论文
共 14 条
[1]  
[Anonymous], 1981, OECD GUID TEST CHEM
[2]   Nature and nurture: Possibilities for cancer control [J].
Doll, R .
CARCINOGENESIS, 1996, 17 (02) :177-184
[3]   MICE DEFICIENT FOR P53 ARE DEVELOPMENTALLY NORMAL BUT SUSCEPTIBLE TO SPONTANEOUS TUMORS [J].
DONEHOWER, LA ;
HARVEY, M ;
SLAGLE, BL ;
MCARTHUR, MJ ;
MONTGOMERY, CA ;
BUTEL, JS ;
BRADLEY, A .
NATURE, 1992, 356 (6366) :215-221
[4]   V-HA-RAS TRANSGENE ABROGATES THE INITIATION STEP IN MOUSE SKIN TUMORIGENESIS - EFFECTS OF PHORBOL ESTERS AND RETINOIC ACID [J].
LEDER, A ;
KUO, A ;
CARDIFF, RD ;
SINN, E ;
LEDER, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9178-9182
[5]  
Lucier George W., 1996, Environmental Health Perspectives, V104, P84, DOI 10.2307/3432764
[6]   Evaluation of transgenic mouse bioassays for identifying carcinogens and noncarcinogens [J].
Tennant, RW ;
Spalding, J ;
French, JE .
MUTATION RESEARCH-REVIEWS IN GENETIC TOXICOLOGY, 1996, 365 (1-3) :119-127
[7]   GENETIC TOXICOLOGY - CURRENT STATUS OF METHODS OF CARCINOGEN IDENTIFICATION [J].
TENNANT, RW ;
ZEIGER, E .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 100 :307-315
[8]   IDENTIFYING CHEMICAL CARCINOGENS AND ASSESSING POTENTIAL RISK IN SHORT-TERM BIOASSAYS USING TRANSGENIC MOUSE MODELS [J].
TENNANT, RW ;
FRENCH, JE ;
SPALDING, JW .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1995, 103 (10) :942-950
[9]  
*US EPA, 1982, 560682001 EPA
[10]  
US Food and Drug Administration Center for Food Safety and Applied Nutrition, 1993, FED REGISTER, V58, P16536