Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients

被引:75
作者
Innes, HE
Liu, D
Barraclough, R
Davies, MPA
O'Neill, PA
Platt-Higgins, A
Rudland, SD
Sibson, DR
Rudland, PS [1 ]
机构
[1] Univ Liverpool, Canc Tissue Bank Res Ctr, Liverpool L69 7ZB, Merseyside, England
[2] JK Douglas Labs, Clatterbridge Canc Res Trust, Wirral CH63 4JY, Merseyside, England
[3] Univ Liverpool, Sch Biol Sci, Liverpool L69 7ZB, Merseyside, England
关键词
AGR2; immunocytochemistry; patient survival; ER alpha-positive breast cancer;
D O I
10.1038/sj.bjc.6603065
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The anterior gradient protein-2 (AGR2) is inducible by oestrogen and itself can induce metastasis in a rat model for breast cancer. Here, a rabbit antibody to recombinant human AGR2 was used to assess its prognostic significance in a retrospective cohort of 351 breast cancer patients treated by adjuvant hormonal therapy. The antibody stains 66% of breast carcinomas to varying degrees. The percentage of positive carcinoma cells in tumours directly correlates with the level of AGR2 mRNA ( Spearman's rank correlation, P = 0.0007) and protein (linear regression analysis r(2) = 0.95, P = 0.0002). There is a significant association of staining of carcinomas for AGR2 with oestrogen receptor alpha (ER alpha) staining and with low histological grade ( both Fisher's Exact test P < 0.0001). In the ER alpha-positive cases, but not the ER alpha-negative cases, when subdivided into the separate staining classes for AGR2, there is a significantly progressive decrease in patient survival with increased staining ( log rank test, P = 0.006). The significant association of staining for AGR2 with patient death over a 10-year period (log rank test P = 0.007, hazard ratio 3) only becomes significant at 6 years of follow-up. This may be due to the cessation of adjuvant hormonal therapy at an earlier time, resulting in adverse re-expression of the metastasis-inducing protein AGR2. British Journal of Cancer (2006).
引用
收藏
页码:1057 / 1065
页数:9
相关论文
共 25 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]  
Altman D.G., 1991, Practical Statistics for Medical Research, DOI [10.1002/sim.4780101015, DOI 10.1002/SIM.4780101015]
[3]   COMPARATIVE EXPRESSION OF FIBROBLAST GROWTH-FACTOR MESSENGER-RNAS IN BENIGN AND MALIGNANT BREAST DISEASE [J].
ANANDAPPA, SY ;
WINSTANLEY, JHR ;
LEINSTER, S ;
GREEN, B ;
RUDLAND, PS ;
BARRACLOUGH, R .
BRITISH JOURNAL OF CANCER, 1994, 69 (04) :772-776
[4]   HORMONE RESISTANCE, INVASIVENESS, AND METASTATIC POTENTIAL IN BREAST-CANCER [J].
CLARKE, R ;
THOMPSON, EW ;
LEONESSA, F ;
LIPPMAN, J ;
MCGARVEY, M ;
FRANDSEN, TL ;
BRUNNER, N .
BREAST CANCER RESEARCH AND TREATMENT, 1993, 24 (03) :227-239
[5]   THE PROCESS OF MALIGNANT PROGRESSION IN HUMAN BREAST-CANCER [J].
CLARKE, R ;
DICKSON, RB ;
BRUNNER, N .
ANNALS OF ONCOLOGY, 1990, 1 (06) :401-407
[6]  
DAVIS CL, 1993, MATER SCI TECH SER, V9, P8, DOI 10.1179/026708393790171494
[7]   Differential modulation of transcriptional activity of estrogen receptors by direct protein-protein interactions with the T cell factor family of transcription factors [J].
El-Tanani, M ;
Fernig, DG ;
Barraclough, R ;
Green, C ;
Rudland, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) :41675-41682
[8]   hAG-2 and hAG-3, human homologues of genes involved in differentiation, are associated with oestrogen receptor-positive breast tumours and interact with metastasis gene C4.4a and dystroglycan [J].
Fletcher, GC ;
Patel, S ;
Tyson, K ;
Adam, PJ ;
Schenker, M ;
Loader, JA ;
Daviet, L ;
Legrain, P ;
Parekh, R ;
Harris, AL ;
Terrett, JA .
BRITISH JOURNAL OF CANCER, 2003, 88 (04) :579-585
[9]   THE PATTERN OF METASTASES IN HUMAN BREAST-CANCER - METHODOLOGICAL ASPECTS AND INFLUENCE OF PROGNOSTIC FACTORS [J].
KAMBY, C .
CANCER TREATMENT REVIEWS, 1990, 17 (01) :37-61
[10]   TRANSFECTED MCF-7 CELLS AS A MODEL FOR BREAST-CANCER PROGRESSION [J].
KERN, FG ;
MCLESKEY, SW ;
ZHANG, L ;
KUREBAYASHI, J ;
LIU, Y ;
DING, IYF ;
KHARBANDA, S ;
CHEN, D ;
MILLER, D ;
CULLEN, K ;
PAIK, S ;
DICKSON, RB .
BREAST CANCER RESEARCH AND TREATMENT, 1994, 31 (2-3) :153-165