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Lookup NU author(s): Dr Joyce Nutt, Kilian Mellon, Professor John LunecORCiD
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The effect of EGF and gefitinib on two EGFR-positive human bladder cancer cell lines has been investigated using array-based gene expression profiling. The most prominent transcript, increased up to 6.7-fold by EGF compared with controls in RT112 cells, was human early growth response protein 1 (hEGR1). This induction was prevented by gefitinib. The hEGR1 mRNA in EGF-treated samples was reduced in the presence of gefitinib, as was hEGR1 protein in cell lysates. In the RT4 cells, hEGR1 expression was halved in the presence of EGF and gefitinib in combination. In bladder tumour samples, there was a significant correlation between hEGR1 mRNA detected by RT-PCR and EGFR detected by ligand binding, (P=0.042). The induction by EGF of the hEGR1 gene, mRNA and protein in RT112 cells, and its inhibition by gefitinib, together with the detection of hEGR1 mRNA in bladder tumours, suggests that hEGR1 may be important in the EGFR growth-signalling pathway in bladder cancer and should be further investigated for its prognostic significance and as a potential therapeutic target. © 2007 Cancer Research.
Author(s): Nutt, J., Foster, P., Mellon, J., Lunec, J.
Publication type: Article
Publication status: Published
Journal: British Journal of Cancer
Year: 2007
Volume: 96
Issue: 5
Pages: 762-768
Print publication date: 12/03/2007
ISSN (print): 0007-0920
ISSN (electronic): 1532-1827
URL: http://dx.doi.org/10.1038/sj.bjc.6603620
DOI: 10.1038/sj.bjc.6603620
PubMed id: 17311025
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