Carey F A
Department of Pathology, University of Edinburgh, U.K.
J Pathol. 1994 Apr;172(4):307-12. doi: 10.1002/path.1711720404.
Nuclear DNA content can be measured in histological and cytological material by the techniques of image and flow cytometry. The measurement depends on the availability of stoichiometric markers for DNA. Results are expressed in DNA histograms from which tumour DNA ploidy and cell proliferation status can be estimated. Flow cytometry analyses large numbers of cells and gives the most meaningful cell cycle data. Image cytometry is more specifically targeted to the population of interest and can accurately measure rare events. A large body of literature exists relating DNA cytometry to clinical outcome, but there are considerable inconsistencies between clinical series which may be due, in many instances, to problems of histogram interpretation and tumour sampling. Rapid 'user-friendly' systems currently under development may increase the clinical acceptance of DNA cytometry.
通过图像和流式细胞术技术,可以在组织学和细胞学材料中测量核DNA含量。该测量取决于用于DNA的化学计量标记物的可用性。结果以DNA直方图表示,从中可以估计肿瘤DNA倍性和细胞增殖状态。流式细胞术分析大量细胞,并给出最有意义的细胞周期数据。图像细胞术更具体地针对感兴趣的群体,并且可以准确测量罕见事件。有大量文献将DNA细胞术与临床结果相关联,但临床系列之间存在相当大的不一致性,在许多情况下,这可能是由于直方图解释和肿瘤采样问题所致。目前正在开发的快速“用户友好”系统可能会提高DNA细胞术的临床接受度。