Intersection of the p63 and NF‐κB pathways in epithelial homeostasis and disease. Issue 9 (8th July 2019)

• Record Type: Journal Article
• Authors: King, Kathryn E.; George, Andrea L.; Sakakibara, Nozomi; Mahmood, Kanwal; Moses, Michael A.; Weinberg, Wendy C.
• Is Part Of: Molecular carcinogenesis. Volume 58:Issue 9(2019)
• Page Start: 1571
• Page End: 1580
• Publication Date: 2019-07-08
• Subjects: c‐Rel -- epidermis -- NF‐κB -- p63 -- squamous cell carcinoma; Carcinogenesis -- Molecular aspects -- Periodicals; 616.994071
• DOI: 10.1002/mc.23081
• Languages: English
• ISSNs: 0899-1987

Abstract

Abstract: Overexpression of ΔNp63α, a member of the p53/p63/p73 family of transcription factors, is a molecular attribute of human squamous cancers of the head and neck, lung and skin. The TP63 gene plays important roles in epidermal morphogenesis and homeostasis, regulating diverse biological processes including epidermal fate decisions and keratinocyte proliferation and survival. When overexpressed experimentally in primary mouse keratinocytes, ΔNp63α maintains a basal cell phenotype including the loss of normal calcium‐mediated growth arrest, at least in part through the activation and enhanced nuclear accumulation of the c‐rel subunit of NF‐κB (Nuclear Factor‐kappa B). Initially identified for its role in the immune system and hematopoietic cancers, c‐Rel has increasingly been associated with solid tumors and other pathologies. ΔNp63α and c‐Rel have been shown to be associated in the nuclei of ΔNp63α overexpressing human squamous carcinoma cells. Together, these transcription factors cooperate in the transcription of genes regulating intrinsic keratinocyte functions, as well as the elaboration of factors that influence the tumor microenvironment (TME). This review provides an overview of the roles of ΔNp63α and c‐Rel in normal epidermal homeostasis and elaborates on how these pathways may intersect in pathological conditions such as cancer and the associated TME.