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PMID: 10502734 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression pattern of the AP-1 family in breast cancer: association of fosB expression with a well-differentiated, receptor-positive tumor phenotype.

International journal of cancer ·Vol. 84 ·No. 5 ·1999-10-22 ·Pages 533-8

Bamberger AM, Methner C, Lisboa BW, Städtler C, Schulte HM, Löning T, Milde-Langosch K

Abstract

In the present study, the expression of members of the AP-1 family of transcription factors in breast tumors (n = 53) was investigated by Western blot with antibodies specific for each of the AP-1 family members (c-jun, junB, junD and c-fos, fosB, fra1 and fra2). The tumors were characterized with regard to grading, staging, histology, steroid-receptor-expression status and c-erbB2/neu expression. For comparison, normal breast-tissue samples, human breast-cancer cell lines (T47D and MDA-MB231) and the transformed human breast epithelial cell line HBL100 were also analyzed. For c-jun, junB, c-fos and fra2, a relatively uniform expression pattern without significant differences among tumors was observed. junD-protein amounts varied strongly in the tumor specimens. fosB-expression levels also varied strongly in the tumors, weak/absent expression being found in 47%, while 45% exhibited strong/very strong levels of expression. While none of the other AP-1 family members showed significant correlations with clinico-pathological tumor parameters or receptor status, expression of fosB was found to correlate significantly with positive steroid-hormone-receptor status (in the tumors and the cell lines) and a more differentiated tumor phenotype. Expression of 2 fra-1-specific bands of 33 and 36.5 kDa showed significant negative correlation with fosB expression, as well as with estrogen-receptor status and differentiation. We conclude that strong differences in the expression pattern of AP-1 family members are present in breast tumors, and that certain members of this family, such as fosB and fra-1, might be involved in the pathogenesis of these tumors.

MeSH Terms
Breast Neoplasms/chemistry,pathology Breast Neoplasms, Male/chemistry Female Humans Male Middle Aged Molecular Weight Phenotype Phosphorylation Proto-Oncogene Proteins c-fos/analysis Proto-Oncogene Proteins c-jun/analysis Receptors, Estrogen/analysis Receptors, Progesterone/analysis Tumor Cells, Cultured
Chemicals
Proto-Oncogene Proteins c-fos Proto-Oncogene Proteins c-jun Receptors, Estrogen Receptors, Progesterone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Bamberger A M
Institute of Pathology, University Hospital, Eppendorf, Hamburg, Germany.
Methner C
Lisboa B W
Städtler C
Schulte H M
Löning T
Milde-Langosch K
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1999-10-22
Pages
533-8
Language
English
Region
United States
NLM ID
0042124
Subset
IM
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