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遗传背景和钍-227作为小鼠骨癌诱发生物模型中的风险因素。

Genetic background and 227Thorium as risk factors in biologically based models for induction of bone cancer in mice.

作者信息

Heidenreich W F, Rosemann M

机构信息

Institute for Radiation Protection, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Neuherberg, Germany.

出版信息

Radiat Environ Biophys. 2012 May;51(2):179-85. doi: 10.1007/s00411-012-0409-x. Epub 2012 Mar 31.

Abstract

We explore the potential for the biologically based two-stage clonal expansion model to make statements about the influence of genetic factors on the steps in the model. We find evidence that the different susceptibility of BALB/C and CBA/Ca mice to bone cancer after (227)Thorium injection may be mostly due to different promotional responses to radiation. In BALB/C × CBA/Ca back-crossed mice, we analyzed the specific contribution of two individual loci in the carcinogenic process. This analysis suggests that the two high- or low-risk alleles are acting on promotion or on the background parameters, but not on radiation-induced initiation. Taken together with the comparison of CBA/Ca and BALB/C mice, this hints at the possibility that the two loci are candidates for modifying radiation-induced promotion.

摘要

我们探讨了基于生物学的两阶段克隆扩增模型对于阐述遗传因素对模型中各步骤影响的潜力。我们发现有证据表明,注射钍(227)后,BALB/C和CBA/Ca小鼠对骨癌的不同易感性可能主要归因于对辐射的不同促癌反应。在BALB/C×CBA/Ca回交小鼠中,我们分析了致癌过程中两个独立基因座的具体作用。该分析表明,两个高风险或低风险等位基因作用于促癌阶段或背景参数,而非辐射诱导的起始阶段。结合CBA/Ca和BALB/C小鼠的比较结果,这暗示这两个基因座有可能是辐射诱导促癌作用的修饰因子。

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