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乳腺癌的细胞遗传学

Cytogenetics of breast cancer.

作者信息

Geleick D, Müller H, Matter A, Torhorst J, Regenass U

机构信息

Research Department, Ciba-Geigy Ltd., Basel, Switzerland.

出版信息

Cancer Genet Cytogenet. 1990 Jun;46(2):217-29. doi: 10.1016/0165-4608(90)90107-l.

Abstract

Chromosome counts were performed on 1,100 cells from 17 malignant breast carcinomas and on 168 cells of four normal tissue samples after amethopterin treatment and G-banding. Karyotypes were established from 216 cells of 11 tumor-derived cultures and from 47 cells of four nonmalignant tissue-derived cultures. Karyotypes of cells from nonmalignant samples showed a normal diploid chromosomal constitution with no consistent loss or gain of a specific chromosome. Structural chromosomal abnormalities were not observed. Tumor-derived cultures could be distinguished from normal cultures on the basis of a significantly increased incidence of numerical changes and structural chromosomal aberrations. In nine of 11 tumor-derived cultures, numerically normal cells were shown to be pseudodiploid, with frequencies ranging to 43% (mean, 13.2%) of the diploid cells. In agreement with previous reports, cytogenetic analyses showed predominantly diploid cells. Clonal numerical changes of chromosomes 17, 18, 20, and 21 could be detected in three tumor samples. Clonal structural abnormalities could be observed in two of 11 analyzed tumours. A t(6;12)(p21;p13) and an enlarged chromosome 7 (7q+) were found in a patient with invasive ductal carcinoma. An inversion of chromosome 7 [inv(7)(q11.2q32)] was observed in one case, also diagnosed as invasive ductal carcinoma. The significance of these findings in relation to clinical data is discussed.

摘要

对17例恶性乳腺癌的1100个细胞以及4个正常组织样本经氨甲蝶呤处理和G显带后的168个细胞进行了染色体计数。从11个肿瘤来源培养物的216个细胞和4个非恶性组织来源培养物的47个细胞中确定了核型。非恶性样本细胞的核型显示为正常二倍体染色体组成,没有特定染色体的一致缺失或增加。未观察到染色体结构异常。肿瘤来源的培养物与正常培养物的区别在于数量变化和染色体结构畸变的发生率显著增加。在11个肿瘤来源的培养物中有9个,数量正常的细胞显示为假二倍体,其频率占二倍体细胞的43%(平均13.2%)。与先前的报告一致,细胞遗传学分析显示主要为二倍体细胞。在3个肿瘤样本中可检测到17、18、20和21号染色体的克隆性数量变化。在11个分析的肿瘤中有2个观察到克隆性结构异常。在1例浸润性导管癌患者中发现了t(6;12)(p21;p13)和一条增大的7号染色体(7q+)。在1例同样诊断为浸润性导管癌的病例中观察到7号染色体倒位[inv(7)(q11.2q32)]。讨论了这些发现与临床数据相关的意义。

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