Mechanisms of the Growth-inhibitory Effect of the RNase-EGF Fused Protein Against EGFR-overexpressing Cells
Background: We previously showed the usefulness of a fused protein of human pancreatic ribonuclease1 (hRNase1) with human epidermal growth factor (hEGF) for molecular targeting of EGF receptor (EGFR)-overexpressing cells. In this study, the mechanisms underlying the inhibition of cell growth by RNas...
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Veröffentlicht in: | Anticancer research 2006-03, Vol.26 (2A), p.857-863 |
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Zusammenfassung: | Background: We previously showed the usefulness of a fused protein of human pancreatic ribonuclease1 (hRNase1) with human
epidermal growth factor (hEGF) for molecular targeting of EGF receptor (EGFR)-overexpressing cells. In this study, the mechanisms
underlying the inhibition of cell growth by RNase-EGF fused proteins was confirmed. Materials and Methods: Des.1-7 hRNase1
was genetically fused to hEGF. The fused proteins were expressed and isolated from Escherichia coli. The internalization of
hRNase1-hEGF was confirmed by confocal fluorescence microscopy. The growth-inhibitory effect of the fused proteins was evaluated
by MTT assay. Results: FITC-labelled hRNase1-hEGF was internalized into EGFR-overexpressing A431 cells. The internalization
was not observed in A431 cells pre-treated with hEGF and EGFR-deficient H69 cells. The growth-inhibitory effect of des.1-7
hRNase1-hEGF against A431 cells was statistically significantly more pronounced than that of hRNase1-hEGF. Conclusion: RNase-EGF
fused proteins are internalized through EGFR and inhibit cell growth by exerting their ribonucleolytic activity in the cytosol. |
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ISSN: | 0250-7005 1791-7530 |