Use of transgenic animals for carcinogenicity testing: Considerations and implications for risk assessment

被引:55
作者
Gulezian, D [1 ]
Jacobson-Kram, D [1 ]
McCullough, CB [1 ]
Olson, H [1 ]
Recio, L [1 ]
Robinson, D [1 ]
Storer, R [1 ]
Tennant, R [1 ]
Ward, JM [1 ]
Neumann, DA [1 ]
机构
[1] Tacon Farms Inc, Madison, CT 06443 USA
关键词
transgenic animals; knockout animals; carcinogenicity testing; risk assessment; carcinogens; bioassay;
D O I
10.1177/019262330002800320
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Advances in genetic engineering have created opportunities for improved understanding of the molecular basis of carcinogenesis. Through selective introduction, activation, and inactivation of specific genes, investigators can produce mice of unique genotypes and phenotypes that afford insights into the events and mechanisms responsible fur tumor formation. It has been suggested that such animals might be used for routine testing of chemicals to determine their carcinogenic potential because the animals may be mechanistically relevant for understanding and predicting the human response to exposure to the chemical bring tested. Before transgenic and knockout mice can he used as an adjunct or alternative to the conventional 2-year rodent bioassay, information related to the animal line to be used, study design, and data analysis and interpretation must be carefully considered. Here, we identify and review such information relative to Tg.AC and rasH2 transgenic mice and p53(+/-) and XPA(-/-) knockout mice, all of which have been proposed For use in chemical carcinogenicity testing. In addition, the implications of findings of tumors in transgenic anti knockout animals when exposed to chemicals is discussed in the context of human health risk assessment.
引用
收藏
页码:482 / 499
页数:18
相关论文
共 149 条
  • [1] TRANSGENIC MODELS OF TUMOR-DEVELOPMENT
    ADAMS, JM
    CORY, S
    [J]. SCIENCE, 1991, 254 (5035) : 1161 - 1167
  • [2] Stable long term germ-line transmission of transgene integration sites in mice
    Aigner, B
    Fleischmann, M
    Müller, M
    Brem, G
    [J]. TRANSGENIC RESEARCH, 1999, 8 (01) : 1 - 8
  • [3] A critical appraisal of the value of the mouse cancer bioassay in safety assessment
    Alden, CL
    Smith, PF
    Piper, CE
    Brej, L
    [J]. TOXICOLOGIC PATHOLOGY, 1996, 24 (06) : 722 - 725
  • [4] Complementation tagging of cooperating oncogenes in knockout mice
    Allen, JD
    Berns, A
    [J]. SEMINARS IN CANCER BIOLOGY, 1996, 7 (05) : 299 - 306
  • [5] MYC-MAX-MAD - A TRANSCRIPTION FACTOR NETWORK CONTROLLING CELL-CYCLE PROGRESSION, DIFFERENTIATION AND DEATH
    AMATI, B
    LAND, H
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) : 102 - 108
  • [6] ANDO K, 1992, CANCER RES, V52, P978
  • [7] [Anonymous], 1995, DIETARY RESTRICTION
  • [8] Berg RJW, 1997, CANCER RES, V57, P581
  • [9] Dermal carcinogenicity in transgenic mice:: Relative responsiveness of male and female hemizygous and homozygous Tg,AC mice to 12-O-tetradecanoylphorbol 13-acetate (TPA) and benzene
    Blanchard, KT
    Ball, DJ
    Holden, HE
    Furst, SM
    Stoltz, JH
    Stoll, RE
    [J]. TOXICOLOGIC PATHOLOGY, 1998, 26 (04) : 541 - 547
  • [10] Bol SAM, 1998, CANCER RES, V58, P2850