Published October 30, 2009 | Version v1
Journal article

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

  • 1. Section of Pathobiology, Department of Veterinary Disease Biology, Dyrlægevej 88, DK-1870 Frederiksberg C (Denmark)
  • 2. Cell and Antibody Analysis, Novo Nordisk A/S, Novo Nordisk Park, DK-2760 Maaloev (Denmark)
  • 3. Molecular Diagnostic Laboratory, Department of Molecular Medicine, Aarhus University Hospital, Skejby, Science Center Skejby, Brendstrupgaardsvej 21, DK-8200 Aarhus N (Denmark)
  • 4. Department of Urology, Aarhus University Hospital, Skejby, DK-8200 Aarhus N (Denmark)
  • 5. Molecular Microbiology, Intercell AG, Campus Vienna Biocenter 3, 1030 Vienna (Austria)

Description

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. 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. 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. 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

Availability note (English)

Available from http://dx.doi.org/10.1186/1471-2407-9-385; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774864

Additional details

Publishing Information

Journal Title
BMC Cancer (Online)
Journal Volume
9
Journal Page Range
p. 385
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46093062
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
BLADDER; GROWTH; HAZARDS; MUSCLES; NEOPLASMS; PATIENTS; TRANSCRIPTION FACTORS; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BODY; DISEASES; ORGANIC COMPOUNDS; ORGANS; PROTEINS; URINARY TRACT

Optional Information

Copyright
Copyright (c)2009 Egerod et al
Notes
PMCID: PMC2774864; PUBLISHER-ID: 1471-2407-9-385; PMID: 19878561; OAI: oai:pubmedcentral.nih.gov:2774864; licensee BioMed Central Ltd.