Cytogenetic evaluation of 20 primary breast carcinomas

被引:7
作者
Cavalli, LR
Cavalieri, LMB
Ribeiro, LA
Cavalli, IJ
Silveira, R
Rogatto, SR
机构
[1] UNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO, DEPT GENET, INST BIOCIENCIAS, BR-18607070 BOTUCATU, SP, BRAZIL
[2] UNIV FED PARANA, DEPT GENET, BR-80060000 CURITIBA, PARANA, BRAZIL
[3] UNIV ESTADUAL LONDRINA, CCB, DEPT BIOL, LONDRINA, PARANA, BRAZIL
[4] HOSP NOSSA SENHORA GRACAS, ONCOL SERV, CURITIBA, PARANA, BRAZIL
来源
HEREDITAS | 1997年 / 126卷 / 03期
关键词
D O I
10.1111/j.1601-5223.1997.00261.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. Six cases showed axillary lymph node metastases. Clonal chromosome abnormalities were detected in all cases. The numerical alterations most frequently observed involved the loss of chromosomes X, 19, 20, and 22 followed by gain of chromosomes 9 and 8. Among the structural anomalies observed, there was preferential involvement of chromosomes 11, 6, 1, 7, 3, and 12, supporting previous reports that these chromosomes may harbour genes of importance in the development of breast tumors. Two cases with a family history of breast cancer had in common total or partial trisomy 1.
引用
收藏
页码:261 / 268
页数:8
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