Integrin β1 upregulation in MCF-7 breast cancer cells by angiotensin II

被引:16
作者
Berry, MG
Goode, AW
Puddefoot, JR
Vinson, GP
Carpenter, R
机构
[1] St Bartholomews Hosp, Dept Surg, St Bartholomews & Royal London Sch Med & Dent, London EC1A 7BE, England
[2] St Bartholomews Hosp, Dept Biochem, St Bartholomews & Royal London Sch Med & Dent, London EC1A 7BE, England
来源
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY | 2000年 / 26卷 / 01期
关键词
human breast cancer; cell adhesion molecules; integrins; angiotensin II;
D O I
10.1053/ejso.1999.0735
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: Integrins are a major family of cell adhesion molecules whose function is perturbed in tumour invasion and metastasis. Angiotensin II (A II) is well-known in the systemic control of water and electrolyte homeostasis and haemodynamics, but recent evidence points to an additional local renin-angiotensin system (RAS) with possible long-term trophic effects including carcinogenesis. Methods: The effect of angiotensin II on MCF-7 human breast cancer cell Line integrin expression was evaluated with immunocytochemistry (ICC) and immunoprecipitation (IP). Results: The experiments demonstrated a 1.40 +/- 0.14-fold increase in beta(1) integrin expression on MCF-7 cells following treatment with A II. Conclusions: These findings report the first evidence of an association between integrins and the RAS in human breast cancer cells and suggest a novel research avenue for future anti-metastatic strategies, through the manipulation of cell adhesion mechanics, in the management of invasive human breast cancer. (C) 2000 Harcourt Publishers Ltd.
引用
收藏
页码:25 / 29
页数:5
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