IRF6 is a mediator of Notch pro-differentiation and tumour suppressive function in keratinocytes

Gaetana Restivo, Bach Cuc Nguyen, Piotr Dziunycz, Elodie Ristorcelli, Russell J H Ryan, Özden Yalçin Özuysal, Matteo Di Piazza, Freddy Radtke, Michael J. Dixon, Günther F L Hofbauer, Karine Lefort, G. Paolo Dotto

    Research output: Contribution to journalArticlepeer-review

    Abstract

    While the pro-differentiation and tumour suppressive functions of Notch signalling in keratinocytes are well established, the underlying mechanisms remain poorly understood. We report here that interferon regulatory factor 6 (IRF6), an IRF family member with an essential role in epidermal development, is induced in differentiation through a Notch-dependent mechanism and is a primary Notch target in keratinocytes and keratinocyte-derived SCC cells. Increased IRF6 expression contributes to the impact of Notch activation on growth/differentiation-related genes, while it is not required for induction of canonical-™ Notch targets like p21 WAF1/Cip1, Hes1 and Hey1. Down-modulation of IRF6 counteracts differentiation of primary human keratinocytes in vitro and in vivo, promoting ras-induced tumour formation. The clinical relevance of these findings is illustrated by the strikingly opposite pattern of expression of Notch1 and IRF6 versus epidermal growth factor receptor in a cohort of clinical SCCs, as a function of their grade of differentiation. Thus, IRF6 is a primary Notch target in keratinocytes, which contributes to the role of this pathway in differentiation and tumour suppression. © 2011 European Molecular Biology Organization | All Rights Reserved.
    Original languageEnglish
    Pages (from-to)4571-4585
    Number of pages14
    JournalEMBO Journal
    Volume30
    Issue number22
    DOIs
    Publication statusPublished - 16 Nov 2011

    Keywords

    • keratinocytes
    • Notch
    • p63
    • squamous cell carcinoma
    • tumour suppression

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