Ashby J, Tinwell H
Zeneca Central Toxicology Laboratory, Nr. Macclesfield, Cheshire, UK.
Mutat Res. 1996 Jun 10;352(1-2):181-4. doi: 10.1016/0027-5107(95)00224-3.
The rodent bone marrow micronucleus (MN) assay occupies a critical position in the accompanying schemes to detect potential human carcinogens and germ cell mutagens (Shelby, 1996; Ashby et al., 1996: for reviews of the MN assay see Heddle et al., 1983; Schlegel and MacGregor, 1984; CSGMT, 1990; Mavournin et al., 1990; Tinwell, 1990; Gatehouse, 1994; Asanami et al., 1995). The intention of this article is to note two perceptional problems currently associated with the MN assay. The first concerns how it should be used--as a screening assay, or as a means to evaluate the genetic toxicity in vivo of genotoxins defined in vitro. The second relates to its sensitivity to the rodent carcinogens defined by the US National Toxicology Program (NTP).
啮齿动物骨髓微核(MN)试验在检测潜在人类致癌物和生殖细胞诱变剂的相关方案中占据关键地位(谢尔比,1996年;阿什比等人,1996年:有关微核试验的综述见赫德尔等人,1983年;施莱格尔和麦格雷戈,1984年;中国遗传毒理学协作组,1990年;马武尔尼等人,1990年;廷韦尔,1990年;盖特豪斯,1994年;浅波等人,1995年)。本文旨在指出目前与微核试验相关的两个认知问题。第一个问题涉及该试验应如何使用——作为一种筛选试验,还是作为评估体外定义的基因毒素体内遗传毒性的手段。第二个问题与其对美国国家毒理学计划(NTP)定义的啮齿动物致癌物的敏感性有关。