Human breast cancer cell lines and tissues express tartrate-resistant acid phosphatase (TRAP)

被引:18
作者
Adams, Lisa M.
Warburton, Michael J.
Hayman, Alison R. [1 ]
机构
[1] Univ Bristol, Sch Clin Vet Sci, Bristol BS40 5DU, Avon, England
[2] St George Hosp, Sch Med, Dept Cellular Pathol, London SW17 0RE, England
关键词
tartrate-resistant; acid phosphatase; breast cancer;
D O I
10.1016/j.cellbi.2006.09.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Tartrate-resistant acid phosphatase (TRAP) is expressed by osteoclasts, macrophages and dendritic cells. TRAP has been identified in a wide variety of tissues, however, its biological function is not fully understood. Serum TRAP is a marker of diseases involving excessive bone resorption including metastatic bone disease in breast cancer patients and can be used to monitor responses to treatment. Our aim in this study was to determine whether TRAP is expressed by human breast tumours. Four breast cancer cell lines were assayed for TRAP activity. MDA-MB-435, the most tumourigenic line, had an activity twofold higher than the other cell lines. Immunohistochemistry using a TRAP specific antibody confirmed that both cell lines and human breast tumours express TRAP. Expression was absent in benign tissues and abundant in more aggressive tumours. This work suggests that tumour derived TRAP contributes to the raised enzyme activity found in the serum of breast cancer patients. (c) 2006 International Federation for Cell Biology. Published-by Elsevier Ltd. All rights reserved.
引用
收藏
页码:191 / 195
页数:5
相关论文
共 30 条
[1]
Tartrate-resistant acid phosphatase is expressed by breast cancer cell lines [J].
Adams, L. M. ;
Warburton, M. J. ;
Hayman, A. R. .
EJC SUPPLEMENTS, 2004, 2 (03) :108-108
[2]
Transgenic mice overexpressing tartrate-resistant acid phosphatase exhibit an increased rate of bone turnover [J].
Angel, NZ ;
Walsh, N ;
Forwood, MR ;
Ostrowski, MC ;
Cassady, AI ;
Hume, DA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (01) :103-110
[3]
Mice lacking tartrate-resistant acid phosphatase (Acp 5) have disordered macrophage inflammatory responses and reduced clearance of the pathogen, Staphylococcus aureus [J].
Bune, AJ ;
Hayman, AR ;
Evans, MJ ;
Cox, TM .
IMMUNOLOGY, 2001, 102 (01) :103-113
[4]
BURSTONE MS, 1958, J NATL CANCER I, V21, P523
[5]
Capeller B, 2003, ANTICANCER RES, V23, P1011
[6]
CHAMBERLAIN P, 1995, CLIN CHEM, V41, P1495
[7]
EKRYLANDER B, 1991, J BIOL CHEM, V266, P24684
[8]
TRACP influences Th1 pathways by affecting dendritic cell function [J].
Esfandiari, Ehsanollah ;
Bailey, Michael ;
Stokes, Christopher R. ;
Cox, Timothy M. ;
Evans, Martin J. ;
Hayman, Alison R. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 (09) :1367-1376
[9]
Halleen JM, 2003, ANTICANCER RES, V23, P1027
[10]
THE INDUCTION OF APOPTOSIS IN HUMAN MAMMARY LUMINAL EPITHELIAL-CELLS BY EXPRESSION OF ACTIVATED C-NEU AND ITS ABROGATION BY GLUCOCORTICOIDS [J].
HARRIS, RA ;
HILES, ID ;
PAGE, MJ ;
OHARE, MJ .
BRITISH JOURNAL OF CANCER, 1995, 72 (02) :386-392