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

被引:30
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.
引用
收藏
页数:8
相关论文
共 34 条
[1]   Impaired prostate tumorigenesis in Egr1-deficient mice [J].
Abdulkadir, SA ;
Qu, ZC ;
Garabedian, E ;
Song, SK ;
Peters, TJ ;
Svaren, J ;
Carbone, JM ;
Naughton, CK ;
Catalona, WJ ;
Ackerman, JJH ;
Gordon, JI ;
Humphrey, PA ;
Milbrandt, J .
NATURE MEDICINE, 2001, 7 (01) :101-107
[2]   Egr1 transcription factor: Multiple roles in prostate tumor cell growth and survival [J].
Adamson, ED ;
Mercola, D .
TUMOR BIOLOGY, 2002, 23 (02) :93-102
[3]  
Barboro P, 2008, CELL ONCOL, V30, P13
[4]   Inhibition of Egr-1 expression reverses transformation of prostate cancer cells in vitro and in vivo [J].
Baron, V ;
De Gregorio, G ;
Krones-Herzig, A ;
Virolle, T ;
Calogero, A ;
Urcis, R ;
Mercola, D .
ONCOGENE, 2003, 22 (27) :4194-4204
[5]   A molecular signature in superficial bladder carcinoma predicts clinical outcome [J].
Dyrskjot, L ;
Zieger, K ;
Kruhoffer, M ;
Thykjaer, T ;
Jensen, JL ;
Primdahl, H ;
Aziz, N ;
Marcussen, N ;
Moller, K ;
Orntoft, AF .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :4029-4036
[6]   Biomarkers for early effects of carcinogenic dual-acting PPAR agonists in rat urinary bladder urothelium in vivo [J].
Egerod, FL ;
Nielsen, HS ;
Iversen, L ;
Thorup, I ;
Storgaard, T ;
Oleksiewicz, MB .
BIOMARKERS, 2005, 10 (04) :295-309
[7]  
EGEROD FL, 2009, J APPL TOXI IN PRESS
[8]  
Eid MA, 1998, CANCER RES, V58, P2461
[9]  
Gohji K, 2001, INT J CANCER, V95, P295, DOI 10.1002/1097-0215(20010920)95:5<295::AID-IJC1051>3.0.CO
[10]  
2-A