Miyamoto H, Kato M, Ishikuro A, Akita H, Kawakami Y
First Department of Medicine, School of Medicine, Hokkaido University, Sapporo, Japan.
Nihon Kyobu Shikkan Gakkai Zasshi. 1992 Dec;30 Suppl:33-8.
Fluorescent in situ hybridization (FISH) with biotinated chromosome-specific repetitive DNA probes was used for the cytogenetic study of lung tumors and three cell lines of human lung cancer. The authors utilized a set of satellite DNA probes, specific for chromosomes 7, 17, X, Y in order to detect numerical chromosome aberrations in tumor cell nuclei. Normal diploid human lymphocyte nuclei, which served as the control, have have two signal spots in 95% of nuclei in response to 7, 17 chromosome probes. However, lung cancer cells have numerical heterogeneity, and copy numbers as determined by FISH were not definite with each probe. Discrepancies between cytogenetic and flow cytometric studies in the detection of aneuploidy in some tumors were shown. The number of FISH spots showed a correlation only with the Ki-67 labeling index expressed in proliferating cells. Loss of the Y chromosome in a high percentage of cells was seen by FISH in some tumors from male patients. These data indicate that FISH with chromosome-specific repetitive DNA probes can serve as a cytogenetic tool for the analysis of interphase nuclei of lung tumors with respect to the detection of numerical chromosome abnormalities.
使用生物素化的染色体特异性重复DNA探针进行荧光原位杂交(FISH),用于肺肿瘤和三种人肺癌细胞系的细胞遗传学研究。作者使用了一组分别针对7号、17号、X染色体和Y染色体的卫星DNA探针,以检测肿瘤细胞核中的染色体数目畸变。作为对照的正常二倍体人淋巴细胞核,在95%的细胞核中,针对7号和17号染色体探针会出现两个信号点。然而,肺癌细胞具有数目异质性,通过FISH确定的每个探针的拷贝数并不明确。结果显示,在某些肿瘤的非整倍体检测中,细胞遗传学研究和流式细胞术研究之间存在差异。FISH信号点的数量仅与增殖细胞中表达的Ki-67标记指数相关。通过FISH在一些男性患者的肿瘤中发现,高比例细胞存在Y染色体缺失。这些数据表明,使用染色体特异性重复DNA探针的FISH可作为一种细胞遗传学工具,用于分析肺肿瘤间期核的染色体数目异常。