Verdoodt B, Castelain P, Bourgain C, Kirsch-Volders M
Laboratory for Anthropogenetics, University Hospital, Brussels, Belgium.
Cancer Genet Cytogenet. 1994 Nov;78(1):53-63. doi: 10.1016/0165-4608(94)90046-9.
Fluorescence in situ hybridization (FISH) with a probe for the pericentromeric region of chromosome 1 and DNA content measurements by image-analysis-based densitometry have been carried out on imprints of benign and malignant breast tissue. In general, an increase in the number of spots per nucleus was observed in the invasive carcinomas, with a large intercellular variation. In comparison with lymphocytes from controls, some cases of benign breast disease already had an increased frequency of aneusomy of chromosome 1, although they were all (near)diploid by DNA-content. However, an overall concordance between the DNA content measurements and the results of FISH was observed, although some exceptions were seen. A statistically significant correlation between the DNA index and the mean number of spots for chromosome 1 per nucleus was found. A linear discriminant analysis was applied on the data; the resulting classification of patients was most accurate when parameters describing DNA content and FISH results were combined.
已使用针对1号染色体着丝粒周围区域的探针进行荧光原位杂交(FISH),并通过基于图像分析的密度测定法对良性和恶性乳腺组织印记进行DNA含量测量。总体而言,在浸润性癌中观察到每个细胞核的斑点数量增加,细胞间差异很大。与对照组的淋巴细胞相比,一些良性乳腺疾病病例已经有1号染色体非整倍体频率增加,尽管它们的DNA含量均为(接近)二倍体。然而,尽管存在一些例外情况,但观察到DNA含量测量结果与FISH结果总体一致。发现DNA指数与每个细胞核1号染色体的平均斑点数之间存在统计学显著相关性。对数据应用线性判别分析;当结合描述DNA含量和FISH结果的参数时,对患者的分类结果最准确。