Expression of the HERI-4 family of receptor tyrosine kinases in breast cancer

被引:498
作者
Witton, CJ
Reeves, JR
Going, JJ
Cooke, TG
Bartlett, JMS
机构
[1] Univ Glasgow, Glasgow Royal Infirm, Dept Surg, Glasgow G31 2ER, Lanark, Scotland
[2] Univ Glasgow, Glasgow Royal Infirm, Dept Pathol, Glasgow G31 2ER, Lanark, Scotland
关键词
HER receptors; EGFR; HER2/neu; c-erbB2; breast cancer; GROWTH-FACTOR RECEPTOR; ERBB SIGNALING NETWORK; ESTROGEN-RECEPTOR; PROTEIN EXPRESSION; PHOSPHATIDYLINOSITOL; 3-KINASE; ALPHA; GENE; OVEREXPRESSION; CARCINOMA; ONCOGENE;
D O I
10.1002/path.1370
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
EGFr/HER1 and c-erbB-2/HER2 expression are associated with poor prognosis in breast cancer. The type I receptor tyrosine kinase (RTK) family to which they belong has four members (HER1-4). In this study, expression of HER1-4 and oestrogen receptor (ER) expression were determined by inmumohistochemistry in 220 breast carcinomas. Elevated expression of HER1 was observed in 16.4%, HER2 in 22.8%, HER3 in 17.5%, and HER4 in 11.9% of these tumours. Patients whose tumours overexpressed HER1, 2 or 3 had reduced survival (p =< 0.001), whereas those whose tumours overexpressed HER4 had increased survival (p = 0.013); 38.6% of cases overexpressed one or more of HER1, 2 or 3. HER4 was rarely overexpressed with other HERs (1.4% of cases). Cox's multiple regression analysis demonstrated that overexpression of HER1/2/3, HER4, and standard prognostic indicators independently affected survival. HER1-3 expression was related to ER negativity (P < 0.0001, chi(2)). Patients with ER-positive, HER1-3-positive tumours had a significantly poorer survival (p < 0.001) than those with ER-positive/HER-negative or HER4-positive tumours. Expression of HER RTKs displays complex interactions between different family members. There is a strong interaction, in terms of survival, between HER expression and ER expression. The development of HER-targeted agents (eg Herceptin, Iressa), and agents targeted at the downstream signalling pathways, therefore provides new possibilities in the treatment of breast cancer. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:290 / 297
页数:8
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