Pandis N, Teixeira M R, Adeyinka A, Rizou H, Bardi G, Mertens F, Andersen J A, Bondeson L, Sfikas K, Qvist H, Apostolikas N, Mitelman F, Heim S
Department of Clinical Genetics, University Hospital, Lund, Sweden.
Genes Chromosomes Cancer. 1998 Jun;22(2):122-9.
Chromosome banding analysis of primary tumors and axillary lymph node metastases from 10 breast cancer patients revealed abnormal karyotypes in all samples with cytogenetic similarities between the primary tumor and the metastasis in all informative pairs. Although karyotypically unrelated clones were also found in the lymph node samples, they were less numerous than in the primary tumors, indicating that there was more genetic heterogeneity among the neoplastic cells in the primary than in the secondary tumors. On the other hand, some of the clones had become more complex in the metastases as a result of clonal evolution, and by and large these metastatic breast cancer cases had more karyotypic anomalies than do unselected primary breast carcinomas. Among the aberrations occurring more frequently, and that consequently may predispose to disease spread, were losses of chromosomes 17 and 22 and homogeneously staining regions, a cytogenetic sign of gene amplification.
对10例乳腺癌患者的原发性肿瘤和腋窝淋巴结转移灶进行染色体显带分析,结果显示所有样本均存在异常核型,且在所有可提供信息的配对中,原发性肿瘤与转移灶之间存在细胞遗传学相似性。尽管在淋巴结样本中也发现了核型不相关的克隆,但它们的数量比原发性肿瘤中的少,这表明原发性肿瘤中肿瘤细胞的遗传异质性比继发性肿瘤中的更多。另一方面,由于克隆进化,一些克隆在转移灶中变得更加复杂,总体而言,这些转移性乳腺癌病例的核型异常比未经选择的原发性乳腺癌更多。在更频繁出现的畸变中,因此可能易导致疾病扩散的是17号和22号染色体的缺失以及均匀染色区,这是基因扩增的细胞遗传学标志。