Predicted anti-oestrogen resistance in BRCA-associated familial breast cancers

被引:42
作者
Osin, P
Gusterson, BA
Philp, E
Waller, J
Bartek, J
Peto, J
Crook, T
机构
[1] Inst Canc Res, Sutton SM2 5NG, Surrey, England
[2] Danish Canc Soc, Div Canc Biol, DK-2100 Copenhagen O, Denmark
关键词
breast; cancer; familial; anti-oestrogen;
D O I
10.1016/S0959-8049(98)00248-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There is controversy concerning the prognosis of breast cancers arising in women carrying loss of function mutations in the breast cancer susceptibility genes BRCA1 and BRCA2. This study was carried out to assess the likely hormone dependence of this group of tumours in comparison with an age and grade matched group of control sporadic tumours. We used quantitative immunohistochemical analysis for the oestrogen receptor (ER), progesterone receptor (PgR), cyclin D1 and pS2 on sections of primary tumours and ductal carcinoma in situ (DCIS). Expression of PgR (P < 0.05) and cyclin D1 (P < 0.01) was low in the BRCA1- and BRCA2-associated cancers compared with sporadic cases. The low frequency of expression of ER (9/40), PgR (2/40) cyclin D1 (5/36) and pS2 (5/36) in the familial tumours indicates that the majority of such tumours will be oestrogen insensitive and unlikely to respond to hormonal manipulation even at the in situ stage in their evolution. The low level of PgR (2/40 cases) suggests that there may be some abnormality of transactivating function of the ER in these tumours. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1683 / 1686
页数:4
相关论文
共 21 条
[1]  
BARTKOVA J, 1995, CANCER RES, V55, P949
[2]   p53 mutations in BRCA1-associated familial breast cancer [J].
Crook, T ;
Crossland, S ;
Crompton, MR ;
Osin, P ;
Gusterson, BA .
LANCET, 1997, 350 (9078) :638-639
[3]   IMMUNOHISTOCHEMICAL AND BIOCHEMICAL-ANALYSIS OF THE ESTROGEN-REGULATED PROTEIN PS2, AND ITS RELATION WITH ESTROGEN-RECEPTOR AND PROGESTERONE-RECEPTOR IN BREAST-CANCER [J].
DETRE, S ;
KING, N ;
SALTER, J ;
MACLENNAN, K ;
MCKINNA, JA ;
DOWSETT, M .
JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (03) :240-244
[4]   A QUICKSCORE METHOD FOR IMMUNOHISTOCHEMICAL SEMIQUANTITATION - VALIDATION FOR ESTROGEN-RECEPTOR IN BREAST CARCINOMAS [J].
DETRE, S ;
JOTTI, GS ;
DOWSETT, M .
JOURNAL OF CLINICAL PATHOLOGY, 1995, 48 (09) :876-878
[5]  
EISENGER F, 1996, CANCER RES, V56, P471
[6]   Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene [J].
Gayther, SA ;
Mangion, J ;
Russell, P ;
Seal, S ;
Barfoot, R ;
Ponder, BAJ ;
Stratton, MR ;
Easton, D .
NATURE GENETICS, 1997, 15 (01) :103-105
[7]   GERMLINE MUTATIONS OF THE BRCA1 GENE IN BREAST AND OVARIAN-CANCER FAMILIES PROVIDE EVIDENCE FOR A GENOTYPE-PHENOTYPE CORRELATION [J].
GAYTHER, SA ;
WARREN, W ;
MAZOYER, S ;
RUSSELL, PA ;
HARRINGTON, PA ;
CHIANO, M ;
SEAL, S ;
HAMOUDI, R ;
VANRENSBURG, EJ ;
DUNNING, AM ;
LOVE, R ;
EVANS, G ;
EASTON, D ;
CLAYTON, D ;
STRATTON, MR ;
PONDER, BAJ .
NATURE GENETICS, 1995, 11 (04) :428-433
[8]  
Gillett C, 1996, INT J CANCER, V69, P92, DOI 10.1002/(SICI)1097-0215(19960422)69:2<92::AID-IJC4>3.0.CO
[9]  
2-Q
[10]   Tumour biological features of BRCA1-induced breast and ovarian cancer [J].
Johannsson, OT ;
Idvall, I ;
Anderson, C ;
Borg, A ;
Barkardottir, RB ;
Egilsson, V ;
Olsson, H .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (03) :362-371