Genetic effects of benzene and radiation in ICR and X Gf mice

B. L. Harper, V. M.S. Ramanujam, L. Kurosky, M. S. Legator

    Research output: Contribution to journalArticlepeer-review

    2 Scopus citations

    Abstract

    X Gf mice (a tumor-resistant strain) were compared with ICR mice (moderately tumorsensitive) for their sensitivity to chromosomal damage caused by benzene, cyclophosphamide (CP), benzo(a)pyrene (BP) and radiation. There was no difference between strains in the level of micronucleus formation caused by BP, CP or radiation. Although X Gf mice metabolized somewhat less of the dose of benzene per weight than ICR mice, and had some-what higher levels of genetic damage, it is not known whether X Gf mice would be measurably more resistant to benzene carcinogenicity. Short-term genotoxicity tests are used as indicators of initiation, therefore, equal sensitivity to a set of standard clastogens suggests that tumor resistance in X Gf mice is a function of later stages of carcinogenesis.

    Original languageEnglish (US)
    Pages (from-to)59-65
    Number of pages7
    JournalCancer Letters
    Volume48
    Issue number1
    DOIs
    StatePublished - Nov 15 1989

    Keywords

    • X Gf mice
    • benzene
    • chromosomes
    • radiation

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

    Fingerprint

    Dive into the research topics of 'Genetic effects of benzene and radiation in ICR and X Gf mice'. Together they form a unique fingerprint.

    Cite this