Imaoka Tatsuhiko, Nishimura Mayumi, Iizuka Daisuke, Daino Kazuhiro, Takabatake Takashi, Okamoto Mieko, Kakinuma Shizuko, Shimada Yoshiya
Experimental Radiobiology for Children's Health Research Group, Research Center for Radiation Protection, National Institute of Radiological Sciences, Japan.
J Radiat Res. 2009 Jul;50(4):281-93. doi: 10.1269/jrr.09027. Epub 2009 Jun 9.
Ionizing radiation is one of a few well-characterized etiologic factors of human breast cancer. Laboratory rodents serve as useful experimental models for investigating dose responses and mechanisms of cancer development. Using these models, a lot of information has been accumulated about mammary gland cancer, which can be induced by both chemical carcinogens and radiation. In this review, we first list some experimental rodent models of breast cancer induction. We then focus on several topics that are important in understanding the mechanisms and risk modification of breast cancer development, and compare radiation and chemical carcinogenesis models. We will focus on the pathology and natural history of cancer development in these models, genetic changes observed in induced cancers, indirect effects of carcinogens, and finally risk modification by reproductive factors and age at exposure to the carcinogens. In addition, we summarize the knowledge available on mammary stem/progenitor cells as a potential target of carcinogens. Comparison of chemical and radiation carcinogenesis models on these topics indicates certain similarities, but it also indicates clear differences in several important aspects, such as genetic alterations of induced cancers and modification of susceptibility by age and reproductive factors. Identification of the target cell type and relevant translational research for human risk management may be among the important issues that are addressed by radiation carcinogenesis models.JRRS Incentive Award in 2009.
电离辐射是少数几种已被充分明确的人类乳腺癌病因之一。实验用啮齿动物是研究癌症发生的剂量反应和机制的有用实验模型。利用这些模型,已经积累了大量关于化学致癌物和辐射均可诱发的乳腺癌的信息。在本综述中,我们首先列出一些诱导乳腺癌的实验性啮齿动物模型。然后,我们重点关注在理解乳腺癌发生机制和风险调节方面重要的几个主题,并比较辐射致癌模型和化学致癌模型。我们将关注这些模型中癌症发生的病理学和自然史、诱导癌症中观察到的基因变化、致癌物的间接影响,以及最后生殖因素和接触致癌物时的年龄对风险的调节。此外,我们总结了关于乳腺干/祖细胞作为致癌物潜在靶点的现有知识。对这些主题的化学致癌模型和辐射致癌模型的比较表明了某些相似之处,但也表明在几个重要方面存在明显差异,如诱导癌症的基因改变以及年龄和生殖因素对易感性的调节。确定靶细胞类型以及针对人类风险管理的相关转化研究可能是辐射致癌模型所涉及的重要问题之一。2009年JRRS激励奖。