Arts, Nathalie
[UCL]
Cané, Stefania
[UCL]
Hennequart, Marc
[UCL]
Lamy, Juliette
[UCL]
Bommer, Guido
[UCL]
Van den Eynde, Benoît
[UCL]
De Plaen, Etienne
[UCL]
Loss of expression of surface antigens represents a significant problem for cancer immunotherapy. Microphthalmia-associated transcription factor (MITF-M) regulates melanocyte fate by driving expression of many differentiation genes, whose protein products can be recognized by cytolytic T lymphocytes. We previously reported that interleukin-1ß (IL-1ß) can downregulate MITF-M levels. Here we show that downregulation of MITF-M expression by IL-1ß was paralleled by an upregulation of miR-155 expression in four melanoma lines. We confirmed that miR-155 was able to target endogenous MITF-M in melanoma cells and demonstrated a role for miR-155 in the IL-1ß-induced repression of MITF-M by using an antagomiR. Notably, we also observed a strong negative correlation between MITF-M and miR-155 levels in a mouse model of melanoma. Taken together, our results indicate that MITF-M downregulation by inflammatory stimuli might be partly due to miR-155 upregulation. This could represent a novel mechanism of melanoma immune escape in an inflammatory microenvironment.
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Référence bibliographique |
Arts, Nathalie ; Cané, Stefania ; Hennequart, Marc ; Lamy, Juliette ; Bommer, Guido ; et. al. microRNA-155, Induced by Interleukin-1ß, Represses the Expression of Microphthalmia-Associated Transcription Factor (MITF-M) in Melanoma Cells. In: PLoS One, Vol. 10, no.4, p. e0122517 (08/04/2015) |
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http://hdl.handle.net/2078.1/158669 |