| Literature DB >> 18772111 |
Bigang Liu1, Xiaojun Xia, Feng Zhu, Eunmi Park, Steve Carbajal, Kaoru Kiguchi, John DiGiovanni, Susan M Fischer, Yinling Hu.
Abstract
It has long been known that excessive mitotic activity due to H-Ras can block keratinocyte differentiation and cause skin cancer. It is not clear whether there are any innate surveillants that are able to ensure that keratinocytes undergo terminal differentiation, preventing the disease. IKKalpha induces keratinocyte terminal differentiation, and its downregulation promotes skin tumor development. However, its intrinsic function in skin cancer is unknown. Here, we found that mice with IKKalpha deletion in keratinocytes develop a thickened epidermis and spontaneous squamous cell-like carcinomas. Inactivation of epidermal growth factor receptor (EGFR) or reintroduction of IKKalpha inhibits excessive mitosis, induces terminal differentiation, and prevents skin cancer through repressing an EGFR-driven autocrine loop. Thus, IKKalpha serves as an innate surveillant.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18772111 PMCID: PMC7263012 DOI: 10.1016/j.ccr.2008.07.017
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743