Suppr超能文献

化学诱导培养的哺乳动物细胞中的非整倍体。

Chemically induced aneuploidy in mammalian cells in culture.

作者信息

Galloway S M, Ivett J L

出版信息

Mutat Res. 1986 Jan-Mar;167(1-2):89-105. doi: 10.1016/0165-1110(86)90011-4.

Abstract

Our objectives were to assess whether there exist useful aneuploidy tests in vitro, to identify chemicals that showed potential for mitotic aneuploidy induction, and to recommend some features of suitable protocols for such testing. From over 100 papers we selected 24 for review. The acceptable studies examined hyperdiploidy at metaphase, had concurrent negative controls with low background rates of hyperdiploidy, used a fixation time sufficient for cells to complete more than one cell cycle after treatment and had multiple dose levels with at least 100 cells scored per point. We judged that 12 compounds were positive, 7 inconclusive, and 4 negative with the reservation that 2 of the 4 compounds had not been tested up to toxic doses. Many of the positive compounds are also known to cause structural chromosome aberrations. We separately reviewed qualitative reports of 'C-mitotic' effects, anaphase lagging, multipolar mitoses, or altered DNA content, since these effects may sometimes by associated with aneuploidy induction. No well-validated in vitro aneuploidy assay exists, and much research is required to develop tests, perhaps using chromosome counts, DNA content, or effects on cell organelles necessary for mitosis. In test protocol development we should carefully consider choice of cell sample size, use of in vitro metabolic activation systems, and selection of doses, especially with regard to the problem of whether cytotoxic concentrations should be used.

摘要

我们的目标是评估体外是否存在有用的非整倍体检测方法,确定显示有诱导有丝分裂非整倍体潜力的化学物质,并为此类检测推荐合适方案的一些特征。我们从100多篇论文中挑选了24篇进行综述。可接受的研究检测了中期的超二倍体,有超二倍体背景率低的同期阴性对照,使用了足以使细胞在处理后完成一个以上细胞周期的固定时间,并有多个剂量水平,每个点至少计数100个细胞。我们判定12种化合物呈阳性,7种结果不确定,4种呈阴性,但保留意见是4种化合物中有2种未测试至有毒剂量。许多阳性化合物也已知会导致染色体结构畸变。我们分别审查了关于“C-有丝分裂”效应、后期滞后、多极有丝分裂或DNA含量改变的定性报告,因为这些效应有时可能与非整倍体诱导有关。目前不存在经过充分验证的体外非整倍体检测方法,开发检测方法可能需要进行大量研究,或许可采用染色体计数、DNA含量或对有丝分裂所需细胞器的影响等方法。在检测方案制定过程中,我们应仔细考虑细胞样本大小的选择、体外代谢活化系统的使用以及剂量的选择,尤其是关于是否应使用细胞毒性浓度这一问题。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验