The relative importance of proliferation and cell death in breast cancer growth and response to tamoxifen

被引:28
作者
Cameron, DA [1 ]
Ritchie, AA
Miller, WR
机构
[1] Univ Edinburgh, Dept Oncol, Edinburgh Breast Res Unit, Edinburgh, Midlothian, Scotland
[2] Western Gen Hosp, Imperial Canc Res Fund, Med Oncol Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
apoptosis; breast cancer; Gompertz; tamoxifen; xenograft;
D O I
10.1016/S0959-8049(01)00166-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Changes in tumour volume depend on the relative balance between cell proliferation and cell loss. However, these processes are not independent, and it remains unclear which is more important in tumour progression and regression. For example, the antioestrogen tamoxifen, a mainstay in the therapy of breast cancer, has both antiproliferative and pro-apoptotic actions, and their relative importance in clinical efficacy is unknown. Thus, using a model system based on oestrogen receptor (ER)-positive ZR-75-1 breast cancer xenografts, both increased apoptosis and reduced proliferation have been previously shown to occur within 7 days of tamoxifen therapy (Cameron DA, Ritchie AA, Langdon S, Anderson TJ, Miller WR. Tamoxifen induced apoptosis in ZR-75 breast cancer xenografts antedates tumour regression. Breast Cancer Res Treat 1997, 45, 99-107). In the present,study, Gompertzian growth curves have been fitted to individual breast cancer xenografts. This demonstrates that the growth rate of the untreated tumours is directly dependent only on the mitotic rate (P <0.001), whereas tumour response to tamoxifen correlates most strongly (P <0.001) with the relative balance between apoptosis and mitosis, as evidenced by the apoptotic: mitotic ratio. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1545 / 1553
页数:9
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