Clinical relevance of immunohistochemical expression of p53-targeted gene products mdm-2, p21 and bcl-2 in breast carcinoma

被引:17
作者
Bánkfalvi, A
Tory, K
Kemper, M
Breukelmann, D
Cubick, C
Poremba, C
Füzesi, L
Lellè, RJ
Böcker, W
机构
[1] Univ Munster, Gerhard Domagk Inst Pathol, D-48149 Munster, Germany
[2] Univ Gottingen, Ctr Pathol, D-3400 Gottingen, Germany
[3] Univ Munster, Dept Obstet & Gynaecol, D-4400 Munster, Germany
关键词
breast cancer; p53; p21; mdm-2; bcl-2; survival; immunohistochemistry; PCR-SSCP;
D O I
10.1016/S0344-0338(00)80051-5
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The present study was designed to investigate the clinical/prognostic relevance of immunohistochemical expression of p53-targeted genes mdm-2, p21(WAF1) and bcl-2 alone and in combination with p53 for the indirect assessment of p53 gene status in breast cancer. 141 archival breast carcinomas were immunostained, and the putative mutational status of the p53 gene was defined in 21 of them, as a control for immunohistochemistry, using the polymerase chain reaction single-strand conformational polymorphism (PCR-SSCP) analysis. Genetic changes of p53 correlated significantly with p53 protein overexpression (p = 0.01) but did not do so with any of the related molecules. Immunohistochemical p53 status was directly correlated with mdm-2 (p = 0.0001), p21 (p = 0.0004) and inversely with bcl-2 (p = 0.005) expression. bcl-2 proved to be an independent marker of prognosis, p,53 only in the group of node-positive carcinomas, whereas bcl-2(-)/p53(+) tumours revealed the worst prognosis. Mdm-2 and p21 expression was of prognostic significance neither alone nor in combination. We conclude that the detection of downstream regulators of p53 does not increase the efficacy of immunohistochemistry in assessing the functional status of p53 in breast cancer; however, their combined analysis may help to select subgroups of patients at the extremes of risk for recurrence, or those with greater chances for survival.
引用
收藏
页码:489 / 501
页数:13
相关论文
共 69 条
[1]  
ALFRED DC, 1993, J NATL CANCER I, V85, P200
[2]  
ALLEN RC, 1989, BIOTECHNIQUES, V7, P736
[3]   PROGNOSTIC-SIGNIFICANCE OF TP53 ALTERATIONS IN BREAST-CARCINOMA [J].
ANDERSEN, TI ;
HOLM, R ;
NESLAND, JM ;
HEIMDAL, KR ;
OTTESTAD, L ;
BORRESEN, AL .
BRITISH JOURNAL OF CANCER, 1993, 68 (03) :540-548
[4]   WET AUTOCLAVE PRETREATMENT FOR ANTIGEN RETRIEVAL IN DIAGNOSTIC IMMUNOHISTOCHEMISTRY [J].
BANKFALVI, A ;
NAVABI, H ;
BIER, B ;
BOCKER, W ;
JASANI, B ;
SCHMID, KW .
JOURNAL OF PATHOLOGY, 1994, 174 (03) :223-228
[5]   ISOLATION OF HUMAN-P53-SPECIFIC MONOCLONAL-ANTIBODIES AND THEIR USE IN THE STUDIES OF HUMAN P53 EXPRESSION [J].
BANKS, L ;
MATLASHEWSKI, G ;
CRAWFORD, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (03) :529-534
[6]   p21(WAF1) immunohistochemical expression in breast carcinoma: Correlations with clinicopathological data, oestrogen receptor status, MIB1 expression, p53 gene and protein alterations and relapse-free survival [J].
Barbareschi, M ;
Caffo, O ;
Doglioni, C ;
Fina, P ;
Marchetti, A ;
Buttitta, F ;
Leek, R ;
Morelli, L ;
Leonardi, E ;
Bevilacqua, G ;
DallaPalma, P ;
Harris, AL .
BRITISH JOURNAL OF CANCER, 1996, 74 (02) :208-215
[7]   COMPLETE SEQUENCING OF THE P53 GENE PROVIDES PROGNOSTIC INFORMATION IN BREAST-CANCER PATIENTS, PARTICULARLY IN RELATION TO ADJUVANT SYSTEMIC THERAPY AND RADIOTHERAPY [J].
BERGH, J ;
NORBERG, T ;
SJOGREN, S ;
LINDGREN, A ;
HOLMBERG, L .
NATURE MEDICINE, 1995, 1 (10) :1029-1034
[8]  
BIER B, 1995, HISTOCHEM J, V27, P148
[9]  
BOSARI S, 1995, VIRCHOWS ARCH, V427, P229
[10]  
Caffo O, 1996, CLIN CANCER RES, V2, P1591