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 Signalling in the epidermis: the E2F cell cycle regulatory pathway in epidermal  morphogenesis, regeneration and transformation Ivanova IA; D'Souza SJ; Dagnino LInt J Biol Sci  2005[]; 1 (2): 87-95The epidermis is the outermost layer in the skin, and it is the first line of  defence against the environment. The epidermis also provides a barrier against  loss of fluids and electrolytes, which is crucial for life. Essential in the  maintenance of this tissue is its ability to continually self-renew and  regenerate after injury. These two characteristics are critically dependent on  the ability of the principal epidermal cell type, the keratinocyte, to  proliferate and to respond to differentiation cues. Indeed, the epidermis is a  multilayered tissue composed of keratinocyte stem cells and their differentiated  progeny. Central for the control of cell proliferation is the E2F transcription  factor regulatory network. This signaling network also includes cyclins, cdk, cdk  inhibitors and the retinoblastoma (pRb) family of proteins. The biological  importance of the E2F/pRb pathway is emphasized by the fact that a majority of  human tumours exhibit alterations that disrupt the ability of pRb proteins to  inhibit E2F, leading to permanent activation of the latter. Further, E2F is  essential for normal epidermal regeneration after injury. Other member of the E2F  signaling pathway are also involved in epidermal development and pathophysiology.  Thus, whereas the pRb family of proteins is essential for epidermal  morphogenesis, abnormal regulation of cyclins and E2F proteins results in  tumorgenesis in this tissue. In this review, we discuss the role of each member  of this important growth regulatory network in epidermal formation, homeostasis  and carcinogenesis.|Animals[MESH]|Cell Cycle Proteins/physiology[MESH]|Cell Transformation, Neoplastic[MESH]|Cyclins/physiology[MESH]|E2F Transcription Factors/*physiology[MESH]|Epidermal Cells[MESH]|Epidermis/embryology/*physiology[MESH]|Gene Expression Regulation/*physiology[MESH]|Homeostasis[MESH]|Humans[MESH]|Keratinocytes/metabolism[MESH]|Mammals/physiology[MESH]|Mice[MESH]|Mice, Knockout[MESH]|Mice, Transgenic[MESH]|Morphogenesis/physiology[MESH]|Neoplasm Proteins/physiology[MESH]|Regeneration/physiology[MESH]|Retinoblastoma Protein/physiology[MESH]|Signal Transduction/*physiology[MESH]|Skin Neoplasms/*physiopathology[MESH]|Skin/injuries[MESH]
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