EXPRESSION OF BETA-1 INTEGRINS IN NONNEOPLASTIC MAMMARY EPITHELIUM, FIBROADENOMA AND CARCINOMA OF THE BREAST
EXPRESSION OF BETA-1 INTEGRINS IN NONNEOPLASTIC MAMMARY EPITHELIUM, FIBROADENOMA AND CARCINOMA OF THE BREAST
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DOI:
10.1007/bf01621803
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发表时间:
1993-03-01
期刊:
影响因子:
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通讯作者:
MOLLER, P
中科院分区:
文献类型:
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作者:
MECHTERSHEIMER, G;MUNK, M;MOLLER, P
Beta1 Integrins were examined immunohistochemically in normal and mastopathic mammary glands, 12 benign tumours and 90 carcinomas of the breast using monoclonal antibodies against beta1 and alpha1 to alpha6 subunits. When compared with epithelial cells of non-neoplastic mammary glands and of benign tumours, carcinoma cells showed considerable quantitative changes in the pattern of alpha2, alpha3 and alpha6 subunit expression. In contrast, the distribution pattern of beta1, alpha1, alpha4 and alpha5 antigens corresponded to the situation observed in non-neoplastic mammary gland epithelium in most instances. An abnormal expression of alpha2 was found in 71.0% of the carcinomas ranging from a remarkably low number of alpha2-positive tumour cells in 27.5% of the cases to a complete absence of the alpha2 molecule in 43.5% of the carcinomas. Of the carcinomas 39.9% exhibited quantitative changes in alpha3 expression with an abnormally low content of alpha3-positive neoplastic cells in 15.4% and a complete absence of this molecule in 24.5% of the cases. Expression of alpha6 was abnormal in 73.2% of the carcinomas, consisting in a greater number of alpha6-negative tumour cells in 31.9% and in a complete absence of alpha6 in 41.3% of the tumours. The abnormally low expression/absence of alpha2 and alpha3 subunits correlated with oestrogen receptor negativity (P < 0.033 and P < 0.04, respectively). In addition, abnormally low expression/absence of alpha2 correlated with poor differentiation of the tumours (P < 0.014). The quantitative changes in the expression pattern of beta1-associated alpha subunits in breast carcinomas may cause a disturbed cell-cell and/or cell-matrix interaction that increases the invasive and migratory property of the tumour cells.