Strong reduction of AGO2 expression in melanoma and cellular consequences
Voeller D, Reinders J, Meister G, Bosserhoff AK (2013)
Publication Type: Journal article
Publication year: 2013
Journal
Book Volume: 109
Pages Range: 3116-3124
Journal Issue: 12
DOI: 10.1038/bjc.2013.646
Abstract
Background:Processing of microRNAs (miRNAs) is a highly controlled process. Deregulation of miRNA expression was observed in several types of cancer but changes in the miRNA-processing enzymes have not been analysed until today. In this study, we analysed Argonaute2 (AGO2, EIF2C2), as one main factor of the miRNA processing ensemble, in the context of cancer development, especially in melanoma.Methods:We determined the AGO2 expression level in melanoma, as well as in other cancers, with biochemical approaches (qRT-PCR, western blot and immunofluorescence studies) and analysed the cell behaviour in migration assays.Results:Specifically in melanoma, we revealed a strong reduction of AGO2 expression compared with primary melanocytes. The reduction of AGO2 expression was only found on protein level, whereas the mRNA level stayed unchanged hinting to post-transcriptional regulation. We could show that re-expression of AGO2 in melanoma leads to a strong improvement of regulatory effects due to increased functionality of small-interfering RNAs and short hairpin RNAs.Conclusion:We identified melanoma-specific downregulation of AGO2 and corresponding reduced RNAi efficiency. These findings will help to understand the molecular basis of malignant melanoma and can potentially lead to an improvement of therapeutic strategies. © 2013 Cancer Research UK.
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Germany (DE)How to cite
APA:
Voeller, D., Reinders, J., Meister, G., & Bosserhoff, A.K. (2013). Strong reduction of AGO2 expression in melanoma and cellular consequences. British Journal of Cancer, 109(12), 3116-3124. https://doi.org/10.1038/bjc.2013.646
MLA:
Voeller, D., et al. "Strong reduction of AGO2 expression in melanoma and cellular consequences." British Journal of Cancer 109.12 (2013): 3116-3124.
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