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Background

Transcription factors often play important roles in tumourigenesis. Members of the PEA3 subfamily of ETS-domain transcription factors fulfil such a role and have been associated with tumour metastasis in several different cancers. Moreover, the activity of the PEA3 subfamily transcription factors is potentiated by Ras-ERK pathway signalling, which is itself often deregulated in tumour cells.

Methods

Immunohistochemical patterns of PEA3 expression and active ERK signalling were analysed and mRNA expression levels of PEA3, ER81, MMP-1 and MMP-7 were determined in gastric adenocarcinoma samples.

Results

Here, we have studied the expression of the PEA3 subfamily members PEA3/ETV4 and ER81/ETV1 in gastric adenocarcinomas. PEA3 is upregulated at the protein level in gastric adenocarcinomas and both PEA3/ETV4 and ER81/ETV1 are upregulated at the mRNA level in gastric adenocarcinoma tissues. This increased expression correlates with the expression of a target gene associated with metastasis, MMP-1. Enhanced ERK signalling is also more prevalent in late-stage gastric adenocarcinomas, and the co-association of ERK signalling and PEA3 expression also occurs in late-stage gastric adenocarcinomas. Furthermore, the co-association of ERK signalling and PEA3 expression correlates with decreased survival rates.

Conclusions

This study shows that members of the PEA3 subfamily of transcription factors are upregulated in gastric adenocarcinomas and that the simultaneous upregulation of PEA3 expression and ERK pathway signalling is indicative of late-stage disease and a poor survival prognosis."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.org/dc/terms/identifier"doi:10.1038/bjc.2011.187"xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Guo B."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Sharrocks A.D."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Ang Y.S."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Downey P."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Cummins R."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Gulmann C."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/author"Keld R."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/name"Br J Cancer"xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/pages"124-130"xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/title"PEA3/ETV4-related transcription factors coupled with active ERK signalling are associated with poor prognosis in gastric adenocarcinoma."xsd:string
http://purl.uniprot.org/citations/21673681http://purl.uniprot.org/core/volume"105"xsd:string
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