Selim A G, El-Ayat G, Wells C A
Department of Histopathology, St. Bartholomew's Hospital, St. Bartholomew's and the Royal London School of Medicine and Dentistry, University of London, UK.
J Pathol. 2000 Jun;191(2):138-42. doi: 10.1002/(SICI)1096-9896(200006)191:2<138::AID-PATH611>3.0.CO;2-J.
Amplification of the c-erbB2 oncogene and numerical aberrations of chromosome 17 occur in human breast carcinomas. Apocrine adenosis (AA) of the breast has been shown occasionally to have c-erbB2 overexpression and a possible premalignant potential, but little is known about cellular level genetic alterations in AA of the breast. Fluorescence in situ hybridization (FISH) is a new approach to detect these. In this study, a series of AA was studied by immunohistochemistry for c-erbB2 protein expression and by FISH using dual colour DNA probes for the c-erbB2 gene and the centromeric region of chromosome 17. Cell membrane immunostaining was seen in 10/18 (55.6%) AA cases, but unequivocal c-erbB2 gene amplification or chromosome 17 aneusomy was not seen. The results of this study suggest that c-erbB2 overexpression without amplification may occur early in breast oncogenesis. Amplification and numerical chromosome aberrations may occur later in the pathogenesis of apocrine-derived breast carcinomas.
c-erbB2癌基因的扩增及17号染色体的数目畸变见于人类乳腺癌。乳腺大汗腺腺病(AA)偶尔显示有c-erbB2过表达并有潜在的恶变前期可能,但关于乳腺AA细胞水平的基因改变知之甚少。荧光原位杂交(FISH)是检测这些改变的一种新方法。在本研究中,通过免疫组织化学检测一系列AA中的c-erbB2蛋白表达,并使用针对c-erbB2基因和17号染色体着丝粒区域的双色DNA探针进行FISH检测。在18例AA病例中有10例(55.6%)可见细胞膜免疫染色,但未见到明确的c-erbB2基因扩增或17号染色体非整倍体。本研究结果提示,无扩增的c-erbB2过表达可能在乳腺肿瘤发生早期出现。扩增及染色体数目畸变可能在大汗腺源性乳腺癌发病过程中较晚出现。