Prognostic values of ETS-1, MMP-2 and MMP-9 expression and co-expression in breast cancer patients

被引:42
作者
Puzovic, V. [1 ]
Brcic, I. [2 ]
Ranogajec, I. [3 ]
Jakic-Razumovic, J. [2 ]
机构
[1] Gen Hosp Dubrovnik, Dept Pathol Cytol & Forens Med, Dubrovnik, Croatia
[2] Univ Zagreb, Ctr Hosp, Dept Pathol, Zagreb 10000, Croatia
[3] Policlin SUNCE, Dept Clin Cytol, Zagreb 10000, Croatia
关键词
breast cancer; ETS-1; gelatinases; transcription factor; prognosis; MATRIX METALLOPROTEINASE-2 MMP-2; TRANSCRIPTION FACTOR; CARCINOMA; MATRIX-METALLOPROTEINASE-9; OVEREXPRESSION; SURVIVAL; INVASION; RELAPSE; GENES; RISK;
D O I
10.4149/neo_2014_054
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to analyse expression of ETS-1 protein and two gelatinases (MMP-2 and MMP-9) and their possible prognostic value in breast carcinoma patients, as well as correlation of their expression with other known prognostic factors such as tumor size, grade, vascular invasion, steroid receptor values, HER2 values and proliferative index. The expression of MMP-2, MMP-9 and ETS-1 was immunohistochemicaly analysed in 121 consecutive primary breast carcinoma patients who underwent surgery at the Clinical Hospital Centre Zagreb during 2002. Three representative areas from each tumor paraffin blocks were taken and arranged on a recipient paraffin block with predefined coordinates for simultaneous analyses of multiple tissue samples (TMA). ETS-1, MMP-2 and MMP-9 expression and co-expression were correlated with other clinico-pathological parameters and based on the available clinical follow up data survival analysis was performed. The ETS-1 protein is found to be expressed in tumor cell nuclei and cytoplasm as well as in stromal lymphocytes, fibroblasts and endothelial cells. MMP-2 and MMP-9 were found to be expressed in cytoplasm of both, tumor and stromal cells. For our analysis only tumor cell expression was used for statistical analysis. We found 56,2% ETS-1 positive tumors, 77,7% were MMP-2 positive, and MMP-9 was expressed in 90% of primary breast carcinomas. There were no significant correlations between MMP-s expression and other patohistological prognostic factors, but expression of ETS-1 was significantly correlated with higher tumor size and grade, as well as with negative steroid receptors. Co-expression of MMP-2, MMP-9 and ETS-1 was found in 40,5 % of tumors, and more commonly was found in tumors larger than 2 cm, high grade tumors, and steroid receptor negative tumors. In univariate analysis, statistically significant negative impact on overall survival (OS) had tumor size, nuclear and tumor grade, ETS-1 expression in tumor cells, co-expression of ETS-1 either with MMP-2 or MMP-9, as well as co-expression of ETS-1, MMP-2 and MMP-3. Disease free survival (DFS) was significantly shorter in patients with tumors greater than 2 cm, ETS-1 positive tumors, ETS-1 and MMP-2 or MMP-9 co-expressed tumors, and additionally in tumors with ETS-1, MMP-2 and MMP-9 co-expression. These results suggest that expression of ETS-1 as well as MMP-2, MMP-9 and ETS-1 co-expression might be used as a poor prognostic factor in breast cancer patients.
引用
收藏
页码:439 / 446
页数:8
相关论文
共 35 条
[1]   Expression of Ets-related transcription factors and matrix metalloproteinase genes in human breast cancer cells [J].
Barrett, JM ;
Puglia, MA ;
Singh, G ;
Tozer, RG .
BREAST CANCER RESEARCH AND TREATMENT, 2002, 72 (03) :227-232
[2]   The Ets-1 transcription factor is up-regulated together with MMP 1 and MMP 9 in the stroma of pre-invasive breast cancer [J].
Behrens, P ;
Rothe, M ;
Wellmann, A ;
Krischler, J ;
Wernert, N .
JOURNAL OF PATHOLOGY, 2001, 194 (01) :43-50
[3]   Gene transfer of matrix metalloproteinase-9 induces tumor regression of breast cancer in vivo [J].
Bendrik, Christina ;
Robertson, Jennifer ;
Gauldie, Jack ;
Dabrosin, Charlotta .
CANCER RESEARCH, 2008, 68 (09) :3405-3412
[4]  
Benson JR, 2012, FUTURE ONCOL, V8, P697, DOI [10.2217/FON.12.61, 10.2217/fon.12.61]
[5]   Overexpression of the Ets-1 transcription factor in human breast cancer [J].
Buggy, Y ;
Maguire, TM ;
McGreal, G ;
McDermott, E ;
Hill, ADK ;
O'Higgins, N ;
Duffy, MJ .
BRITISH JOURNAL OF CANCER, 2004, 91 (07) :1308-1315
[6]   Breast cancer progression: insights into multifaceted matrix metalloproteinases [J].
Chabottaux, Vincent ;
Noel, Agnes .
CLINICAL & EXPERIMENTAL METASTASIS, 2007, 24 (08) :647-656
[7]  
Chang C, 2001, TRENDS CELL BIOL, V11, pS37, DOI 10.1016/S0962-8924(01)82222-4
[8]   Metalloproteinases: role in breast carcinogenesis, invasion and metastasis [J].
Duffy, MJ ;
Maguire, TM ;
Hill, A ;
McDermott, E ;
O'Higgins, N .
BREAST CANCER RESEARCH, 2000, 2 (04) :252-257
[9]   Expression of c-ets-1 mRNA is associated with an invasive, EMT-derived phenotype in breast carcinoma cell lines [J].
Gilles, C ;
Polette, M ;
Birembaut, P ;
Brunner, N ;
Thompson, EW .
CLINICAL & EXPERIMENTAL METASTASIS, 1997, 15 (05) :519-526
[10]   The molecular pathology of hereditary breast cancer:: genetic testing and therapeutic implications [J].
Honrado, E ;
Benítez, J ;
Palacios, J .
MODERN PATHOLOGY, 2005, 18 (10) :1305-1320