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Published in: Breast Cancer Research and Treatment 3/2008

01-02-2008 | Preclinical Study

Role of Fra-2 in breast cancer: influence on tumor cell invasion and motility

Authors: Karin Milde-Langosch, Stanislava Janke, Ines Wagner, Christine Schröder, Thomas Streichert, Ana-Maria Bamberger, Fritz Jänicke, Thomas Löning

Published in: Breast Cancer Research and Treatment | Issue 3/2008

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Abstract

Fra-2 (Fos-related antigen 2) is a member of the Fos family of AP-1 transcription factors which is often up-regulated in mammary carcinomas. Previous results suggested that it might be involved in the regulation of breast cancer invasion and metastasis. In order to analyze the role of Fra-2 in breast cancer cells, it was silenced in the highly invasive MDA-MB231 cells using RNA interference. On the other hand, stable transfectants of the weakly invasive MCF7 cell line were established in order to analyze the effects of Fra-2 overexpression. In both approaches, cell proliferation was not or only weakly influenced by Fra-2. In contrast, the invasive potential of the cells was increased, and a weaker effect on motility was observed. By cDNA microarray analysis of the MCF7 transfectants followed by validation on a protein level, we identified several Fra-2 target genes which might be involved in cell invasion and migration, i.e., ALCAM and connexin 43. Additionally, mRNA expression levels of various genes which are associated with a more malignant behavior of the tumors in vivo were up- or downregulated, i.e., members of the MAGE family, S100P, TIMP2, IL24 etc. These results show that Fra-2 overexpression is associated with a more aggressive tumor phenotype and is probably involved in breast cancer progression in vivo.
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Metadata
Title
Role of Fra-2 in breast cancer: influence on tumor cell invasion and motility
Authors
Karin Milde-Langosch
Stanislava Janke
Ines Wagner
Christine Schröder
Thomas Streichert
Ana-Maria Bamberger
Fritz Jänicke
Thomas Löning
Publication date
01-02-2008
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2008
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-007-9559-y

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