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Anti-oestrogens but not oestrogen deprivation promote cellular invasion in intercellular adhesion-deficient breast cancer cells

Annabel C Borley1 email, Stephen Hiscox2 email, Julia Gee2 email, Chris Smith1 email, Victoria Shaw2 email, Peter Barrett-Lee1 email and Robert I Nicholson2 email

Velindre Cancer Centre, Velindre Road, Cardiff, CF14 2TL, UK

Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, King Edward VII Avenue, Cardiff, CF10 3NB, UK

author email corresponding author email

Breast Cancer Research 2008, 10:R103doi:10.1186/bcr2206

Published: 4 December 2008

Additional files

Additional file 1:

Figure that demonstrates the ability of tamoxifen to promote the invasion, and an increase in Src activation, of an additional ER+ cell line, T47D, following E-cadherin knockdown. T47D cells were treated with non-targeting siRNA control (NT control) or siRNA for E-cadherin (CDH1) in the absence of oestrogen (-E2) or presence of tamoxifen (tam) as described for MCF-7 cells. (a) Cell invasion was assessed using Matrigel invasion assays while changes in E-cadherin expression and Src activity were determined by (b) Western blotting (c) with subsequent densitometry. Tamoxifen promoted significant cell invasion in the absence of E-cadherin expression which was accompanied by an increase in Src kinase activity (Src phosphorylated at Y418).

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