Nm23 gene product expression in invasive breast cancer -: Immunohistochemical analysis and clinicopathological correlation

被引:15
作者
Belev, B
Aleric, I
Vrbanec, D
Petroveceki, M
Unusic, J
Belev, B
机构
[1] Univ Zagreb, Clin Hosp Lung Dis, Sch Med, Dept Pathophysiol,Clin Hosp Rebro, Zagreb 10000, Croatia
[2] Univ Zagreb, Clin Hosp Rebro, Sch Med, Dept Surg, Zagreb 10000, Croatia
[3] Univ Zagreb, Clin Hosp Lung Dis, Sch Med, Dept Pathol,Clin Hosp Rebro, Zagreb 10000, Croatia
[4] Univ Zagreb, Clin Hosp Dubrava, Zagreb, Croatia
关键词
D O I
10.1080/028418602760169406
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The nm23 gene/protein is a putative metastatic suppressor identified a decade ago in a melanoma cell line. A number of laboratory, clinical and pathological studies have been carried out to define its real biological and biochemical function as a step in a complex metastatic process. In our study we examined the significance of nm23 expression in 164 breast cancer patients, aged 35 to 74 years, in comparison to other parameters such as age, menopausal status, histological grade, tumor size, lymph node status, and hormone receptor status. Overall survival (OS) and disease-free survival (DFS) were analyzed. The median follow-up was 84 months. Significant changes in OS were found for tumor size, nodal involvement and histological grade but there was no convincing correlation with nm23 expression. When patients were stratified according to nm23 expression, it was shown that overall survival in nm23-positive patients was no longer than that in nm23 negative patients. It was also shown that patients who were lymph node negative and older than 50 years had longer OS than nm23-negative patients. A statistical analysis shows that there is a correlation between axillary node status and nm23 expression (p = 0.018) as well as between patients' ages and nm23 expression (p = 0.043). There was no statistically significant correlation between nm23 expression, lymph node status and their combination on DFS.
引用
收藏
页码:355 / 361
页数:7
相关论文
共 34 条
[1]  
BACKER JM, 1993, ONCOGENE, V8, P497
[2]   C-erbB-2, p53, and nm23 gene product expression in breast cancer in young women:: Immunohistochemical analysis and clinicopathologic correlation [J].
Bertheau, P ;
Steinberg, SM ;
Merino, MJ .
HUMAN PATHOLOGY, 1998, 29 (04) :323-329
[3]  
Bodey B, 1997, ANTICANCER RES, V17, P505
[4]   NM23 NUCLEOSIDE DIPHOSPHATE KINASE - TOWARD A STRUCTURAL AND BIOCHEMICAL UNDERSTANDING OF ITS BIOLOGICAL FUNCTIONS [J].
DELAROSA, A ;
WILLIAMS, RL ;
STEEG, PS .
BIOESSAYS, 1995, 17 (01) :53-62
[5]   PATHOLOGICAL PROGNOSTIC FACTORS IN BREAST-CANCER .1. THE VALUE OF HISTOLOGICAL GRADE IN BREAST-CANCER - EXPERIENCE FROM A LARGE STUDY WITH LONG-TERM FOLLOW-UP [J].
ELSTON, CW ;
ELLIS, IO .
HISTOPATHOLOGY, 1991, 19 (05) :403-410
[6]   Site-directed mutation of nm23-H1 - Mutations lacking motility suppressive capacity upon transfection are deficient in histidine-dependent protein phosphotransferase pathways in vitro [J].
Freije, JMP ;
Blay, P ;
MacDonald, NJ ;
Manrow, RE ;
Steeg, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) :5525-5532
[7]  
Freije JMP, 1998, BIOCHEM SOC SYMP, P261
[8]  
FREIJE JMP, 1996, ATTEMPTS UNDERSTAND, V2, P215
[9]  
GILLES AM, 1991, J BIOL CHEM, V266, P8784
[10]   Nm23-H1: Genetic alterations and expression patterns in tumor metastasis [J].
Hartsough, MT ;
Steeg, PS .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :6-10