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Updated: Aug 8, 2026

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Published on: November 16, 2011
Fos-transformation activates genes associated with invasion
R F Hennigan1, K L Hawker, B W Ozanne
1Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235.
Abstract:
Fos oncoproteins transform cells by functioning as transcription factors. Over-expression of c-fos results in minimal morphological transformation while the two viral isolates, FBJ and FBR v-fos, result in full morphological transformation. Fos-transformed cells are serum dependent for proliferation but not for morphological transformation. To identify Fos target genes which might be involved in morphological transformation we screened a cDNA library constructed from RNA isolated from serum starved FBR-transformed cells with cDNA probes prepared from both FBR-transformed cells and untransformed parental fibroblasts, 208F. We identified 10 genes which are differentially expressed between FBR and 208F cells. One is a novel gene. Nine are upregulated in c-fos- and FBJ-transformed cells and also in mutant c-Ha-Ras-transformed 208Fs. All nine of the upregulated genes have been associated previously with invasion or metastasis. We demonstrate that the FBR-transformed cells are invasive in an in vitro assay and that their ability to invade is enhanced by platelet derived growth factor. We conclude that the fos oncogenes target genes involved in morphological transformation, and invasion.
Insights
Fos oncoproteins drive cell transformation and invasion by targeting specific genes. This study identified nine genes linked to metastasis, revealing a crucial role for Fos in cancer progression and cell invasion.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Fos oncoproteins act as transcription factors, influencing cell transformation.
- Viral Fos isolates (FBJ, FBR) induce full morphological transformation, unlike c-fos.
- Fos-transformed cells require serum for proliferation but not for morphological changes.
Purpose of the Study:
- Identify Fos target genes responsible for morphological transformation.
- Investigate the role of Fos in cell invasion and metastasis.
Main Methods:
- Screened a cDNA library from serum-starved FBR-transformed cells.
- Utilized cDNA probes from FBR-transformed and parental 208F fibroblasts.
- Performed in vitro invasion assays.
Main Results:
- Identified 10 differentially expressed genes; one is novel.
- Nine genes were upregulated in Fos- and Ras-transformed cells.
- Upregulated genes are associated with invasion and metastasis.
- FBR-transformed cells demonstrated invasiveness, enhanced by platelet-derived growth factor.
Conclusions:
- Fos oncogenes target genes critical for morphological transformation.
- Fos oncogenes also target genes involved in cell invasion and metastasis.
- Fos plays a significant role in cancer progression through gene regulation.
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