Parry J M
School of Biological Sciences, University College of Swansea, Great Britain.
Mutat Res. 1988 May-Aug;205(1-4):385-92. doi: 10.1016/0165-1218(88)90028-6.
Many individual Mutagenicity Guidelines contain suggested test systems with choices of such parameters as strains, cell types and even endpoint assayed. Comparisons have been made of data obtained from variants of yeast assays for the induction of mitotic recombination, in vitro assays for the induction of chromosome aberrations and assays for the induction of cell transformation. Individual test variants included in guidelines of the EEC and OECD show considerable qualitative and quantitative variability of response to potential mutagens and carcinogens. Such variability between assays within the same guideline raises considerable problems in the selection of test batteries chosen from published Mutagenicity Guidelines. Improved battery selection is dependent upon the reduction of choice within guidelines to those assays which produce consistent and reproducible results.
许多单独的致突变性指南都包含了一些建议的测试系统,并提供了诸如菌株、细胞类型甚至所检测的终点等参数的选择。人们对从酵母有丝分裂重组诱导试验的变体、体外染色体畸变诱导试验以及细胞转化诱导试验中获得的数据进行了比较。欧洲经济共同体(EEC)和经济合作与发展组织(OECD)指南中包含的各个测试变体显示,对潜在诱变剂和致癌物的反应在定性和定量方面都存在相当大的变异性。同一指南内不同试验之间的这种变异性,在从已发表的致突变性指南中选择测试组合时引发了相当大的问题。改进测试组合的选择取决于将指南中的选择减少到那些能产生一致且可重复结果的试验。