High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression

被引:29
作者
Egerod, Frederikke Lihme [1 ,2 ]
Bartels, Annette [2 ]
Fristrup, Niels [3 ]
Borre, Michael [4 ]
Orntoft, Torben F. [3 ]
Oleksiewicz, Martin B. [5 ]
Brunner, Nils [2 ]
Dyrskjot, Lars [3 ]
机构
[1] Novo Nordisk AS, Cell & Antibody Anal, DK-2760 Malov, Denmark
[2] Dept Vet Dis Biol, Sect Pathobiol, DK-1870 Frederiksberg C, Denmark
[3] Aarhus Univ Hosp, Mol Diagnost Lab, Dept Mol Med, Sci Ctr Skejby, DK-8200 Aarhus N, Denmark
[4] Aarhus Univ Hosp, Dept Urol, DK-8200 Aarhus N, Denmark
[5] Intercell AG, Mol Microbiol, A-1030 Vienna, Austria
来源
BMC CANCER | 2009年 / 9卷
关键词
HUMAN PROSTATE-CANCER; HEPARANASE EXPRESSION; TRANSCRIPTION FACTOR; HYAL1; HYALURONIDASE; EGF RECEPTOR; IN-VIVO; GROWTH; PROMOTER; BIOMARKERS; DIAGNOSIS;
D O I
10.1186/1471-2407-9-385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Egr-1 (early growth response-1 transcription factor) has been proposed to be involved in invasion and metastasis processes of human bladder cancer, but Egr-1 protein expression levels in human bladder cancer have not been investigated. In the present study we investigated the expression levels of Egr-1 protein in early stages of human bladder cancer and correlated it to later progression. Methods: Expression of Egr-1 protein in human bladder cancer was examined by immunohistochemistry, on a tissue microarray constructed from tumors from 289 patients with non-muscle invasive urothelial bladder cancer. Results: The frequency of tumor cells with nuclear Egr-1 immunolabelling correlated to bladder cancer stage, grade and to later progression to muscle-invasive bladder cancer (T2-4). Stage T1 tumors exhibited significantly higher frequencies of tumor cells with nuclear Egr-1 immunolabelling than Ta tumors (P = 0.001). Furthermore, Kaplan-Meier survival analysis showed that a high frequency of tumor cells with nuclear Egr-1 immunolabelling was significantly associated with a higher risk of progression to stage T2-4 (log-rank test, P = 0.035). Tumor cells with nuclear Egr-1 immunolabelling were found to localize at the tumor front in some of the tumor biopsies. Conclusion: The results from this study support a potential involvement of Egr-1 in the progression from non-muscle invasive bladder cancers to muscle invasive bladder cancer.
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页数:8
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