Herrington C S, Leek R D, McGee J O
Nuffield Department of Pathology and Bacteriology, University of Oxford, John Radcliffe Hospital, U.K.
J Pathol. 1995 Aug;176(4):353-9. doi: 10.1002/path.1711760406.
Abnormalities of chromosomes 11 and 17 have been widely reported in invasive carcinoma of the breast. Interphase cytogenetics using pericentromeric repeat probes allows the evaluation of numerical chromosomal aberrations in tumour cell populations. We have developed a method for interphase cytogenetics on fine needle aspirates taken from breast tumours and have applied it to the analysis of chromosomes 11 and 17 in 49 cases of invasive adenocarcinoma. Frequency distributions of signal number were generated for each case and no correlation was found between modal signal number and tumour size at presentation, nodal status or tumour differentiation. In 14 cases, two copies of each of chromosomes 11 and 17 were present, and in 14, the number of chromosomes 11 and 17 were equal but abnormal. In 14 cases, the chromosome 11 number was greater than chromosome 17 and in 7 cases, the chromosome 17 number was greater than chromosome 11. Chromosome inequality correlated with the presence of lymph node metastases or disseminated disease at presentation and the absence of in situ carcinoma. There was no relationship with the presence of vascular invasion. These data suggest that numerical chromosome 11 and 17 imbalance may indicate the ability of breast cancers to metastasize rather than invade vessels. The pattern of numerical chromosome abnormality described may define a subgroup of tumours with a greater tendency for metastasis.
11号和17号染色体异常在乳腺浸润癌中已有广泛报道。使用着丝粒周围重复探针的间期细胞遗传学可用于评估肿瘤细胞群体中的染色体数目畸变。我们已开发出一种针对乳腺肿瘤细针穿刺样本进行间期细胞遗传学分析的方法,并将其应用于49例浸润性腺癌中11号和17号染色体的分析。为每个病例生成信号数的频率分布,未发现众数信号数与就诊时肿瘤大小、淋巴结状态或肿瘤分化之间存在相关性。在14例病例中,11号和17号染色体各有两份拷贝;在14例中,11号和17号染色体数目相等但异常。在14例病例中,11号染色体数目大于17号染色体;在7例病例中,17号染色体数目大于11号染色体。染色体数目不等与就诊时存在淋巴结转移或播散性疾病以及不存在原位癌相关。与血管侵犯的存在无关。这些数据表明,11号和17号染色体数目失衡可能表明乳腺癌的转移能力而非血管侵犯能力。所描述的染色体数目异常模式可能定义了一个具有更高转移倾向的肿瘤亚组。