Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F
Department of Clinical Genetics, Lund University Hospital, Sweden.
Genes Chromosomes Cancer. 1993 Jan;6(1):51-7. doi: 10.1002/gcc.2870060110.
Short-term cultures from 20 breast carcinomas were analyzed cytogenetically. A normal female chromosome complement was found in 4 cases. Clonal chromosome aberrations were detected in 16 tumors. In 10 tumors, multiple cytogenetic clones were found; in 2 cancers the clones were related, reflecting clonal evolution, but in the remaining 8 tumors the clones were cytogenetically unrelated, indicating clonal heterogeneity in the origin of the tumor parenchyma. Correlation analysis between karyotypic and pathologic parameters indicated that cases with complex karyotypes and/or cytogenetically unrelated clones, when compared with cases with a single simple karyotypic abnormality, were generally of higher histologic malignancy grade, had more mitoses in the histologic sections, and also more often had carcinoma in situ lesions in the same breast.
对20例乳腺癌的短期培养物进行了细胞遗传学分析。4例中发现有正常女性染色体组成。16例肿瘤检测到克隆性染色体畸变。10例肿瘤中发现多个细胞遗传学克隆;2例癌症中的克隆相关,反映了克隆进化,但其余8例肿瘤中的克隆在细胞遗传学上不相关,表明肿瘤实质起源存在克隆异质性。核型与病理参数的相关性分析表明,与单一简单核型异常的病例相比,具有复杂核型和/或细胞遗传学不相关克隆的病例通常组织学恶性程度更高,组织切片中有更多的有丝分裂,并且同一乳腺中也更常出现原位癌病变。