IRF6 is a mediator of Notch pro-differentiation and tumour suppressive function in keratinocytes.
| Data(s) |
2011
|
|---|---|
| Resumo |
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. |
| Identificador |
http://serval.unil.ch/?id=serval:BIB_61CE22FDB0C0 isbn:1460-2075 (Electronic) pmid:21909072 doi:10.1038/emboj.2011.325 isiid:000297691500006 |
| Idioma(s) |
en |
| Fonte |
EMBO Journal, vol. 30, no. 22, pp. 4571-4585 |
| Palavras-Chave | #Animals; Basic Helix-Loop-Helix Transcription Factors/metabolism; Cell Cycle Proteins/metabolism; Cell Differentiation; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21/metabolism; Cyclin-Dependent Kinase Inhibitor p21/physiology; DNA-Binding Proteins/metabolism; Genes, Tumor Suppressor; Homeodomain Proteins/metabolism; Humans; Interferon Regulatory Factors/biosynthesis; Interferon Regulatory Factors/genetics; Keratinocytes/cytology; Keratinocytes/metabolism; Mice; Mice, Inbred NOD; Mice, SCID; Oncogene Protein p21(ras)/metabolism; Promoter Regions, Genetic; RNA Interference; RNA, Small Interfering; Receptor, Epidermal Growth Factor/biosynthesis; Receptor, Epidermal Growth Factor/genetics; Receptor, Notch1/genetics; Receptor, Notch1/metabolism; Signal Transduction; Skin Neoplasms/metabolism; Skin Neoplasms/pathology |
| Tipo |
info:eu-repo/semantics/article article |