Activated ERK1/2 and phosphorylated oestrogen receptor α are associated with improved breast cancer survival in women treated with tamoxifen

The aim of this study was to investigate the expression of activated (phosphorylated) ERK1/2, oestrogen receptor alpha phosphorylated at S118 (ER alpha(S118)), and HER2 in primary breast cancer, and to make correlations with the outcome of tamoxifen therapy We performed immunohistochemical analysis to determine the expression of HER2, ER alpha(S118), and activated ERK1/2 in tumours obtained from 279 women with primary breast cancer. HER2 status was also estimated by fluorescence in situ hybridisation. We identified 108 women with ER alpha-positive tumours who had received adjuvant tamoxifen. Activated ERK1/2 (pERK1/2) and ER alpha(S118) were found to be associated with each other and with other factors correlated with good prognosis. HER2 was inversely associated with pERK1/2. Positive staining for pERK1/2 (particularly intense staining) indicated better relapse-free survival (P = 0.05) and a trend towards better breast cancer-corrected survival in women treated with tamoxifen. To conclude, this study shows that activated ERK1/2 and ER alpha(S118) are associated with improved survival. The poorer outcome in HER2-positive women who receive adjuvant tamoxifen cannot be explained by the crosstalk between HER2 and ER alpha(S118) via activated ERK1/2 alone. (c) 2006 Elsevier Ltd. All rights reserved.