Glei Michael, Hovhannisyan Galina, Pool-Zobel Beatrice L
Department of Nutritional Toxicology, Institute for Nutrition, Friedrich-Schiller-University Jena, Dornburger Street 24, 07743 Jena, Germany.
Mutat Res. 2009 Jan-Feb;681(1):33-43. doi: 10.1016/j.mrrev.2008.01.006. Epub 2008 Jan 31.
The Comet-FISH technique is a useful tool to detect overall and region-specific DNA damage and repair in individual cells. It combines two well-established methods, the Comet assay (single cell gel electrophoresis) and the technique of fluorescence in situ hybridization (FISH). Whereas the Comet assay allows separating fragmented from non-fragmented DNA, FISH helps to detect specifically labelled DNA sequences of interest, including whole chromosomes. Thus the combination of both techniques has been applied in particular for detection of site-specific breaks in DNA regions which are relevant for development of different diseases. This paper reviews the relevant literature and presents three examples on how Comet-FISH was used for studying the induction of DNA damage by genotoxic compounds related to oxidative stress in colon cancer-relevant genes (TP53, APC, KRAS) of a colon adenoma cell line. The accumulated evidence on relative sensitivity of these genes in comparison to global damage allows a more definite conclusion on the possible contribution of the genotoxic factors during colorectal carcinogenesis. Telomere fragility was compared in different cell lines treated with cytostatic agents, and revealed new patterns of biological activities through the drugs and different sensitivities of the cell lines that were found to be associated with their tumour origin. A third example relates to measuring repair of specific gene regions using Comet-FISH, a method that can be developed to biomarker application. Taken together, available data suggests that Comet-FISH helps to get further insights into sensitivity of specific DNA regions and consequently in mechanisms of carcinogenesis. Although the nature of the measured Comet-FISH endpoint precludes us from stating basically that damage and repair are occurring within the specific gene, it is at least possible to evaluate whether the damage and repair are occurring within the vicinity of the gene of interest.
彗星荧光原位杂交(Comet-FISH)技术是检测单个细胞中整体及区域特异性DNA损伤与修复的有用工具。它结合了两种成熟的方法,即彗星试验(单细胞凝胶电泳)和荧光原位杂交(FISH)技术。彗星试验能够分离断裂的和未断裂的DNA,而FISH有助于检测感兴趣的特异性标记DNA序列,包括整条染色体。因此,这两种技术的结合尤其适用于检测与不同疾病发生相关的DNA区域中的位点特异性断裂。本文综述了相关文献,并给出了三个实例,介绍了如何利用彗星荧光原位杂交技术研究结肠腺瘤细胞系中与氧化应激相关的遗传毒性化合物在结肠癌相关基因(TP53、APC、KRAS)中诱导DNA损伤的情况。与整体损伤相比,这些基因相对敏感性的累积证据使我们能够更明确地得出遗传毒性因素在结直肠癌发生过程中可能作用的结论。比较了用细胞抑制剂处理的不同细胞系中的端粒脆性,并通过药物揭示了新的生物活性模式以及发现与肿瘤起源相关的细胞系的不同敏感性。第三个实例涉及使用彗星荧光原位杂交技术测量特定基因区域的修复情况,该方法可发展用于生物标志物应用。综上所述,现有数据表明彗星荧光原位杂交技术有助于进一步深入了解特定DNA区域的敏感性,从而深入了解致癌机制。尽管测量的彗星荧光原位杂交终点的性质使我们无法从根本上说明损伤和修复是否发生在特定基因内,但至少可以评估损伤和修复是否发生在感兴趣基因的附近。