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      PFKFB3, a direct target of p63, is required for proliferation and inhibits differentiation in epidermal keratinocytes

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      1 , 1
      The Journal of investigative dermatology

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          Abstract

          p63 is a transcription factor essential for epidermal development and homeostasis. p63 is a member of the p53 family of transcription factors, which are increasingly understood to be regulators of cellular metabolism. How p63 regulates metabolism in epidermal keratinocytes is incompletely understood, and it is unknown whether glycolytic regulation is essential to maintain the balance between proliferation and differentiation within the epidermis. We found that p63 promotes glycolytic metabolism in epidermal keratinocytes. p63 bound to consensus sites within the PFKFB3 gene and was required for PFKFB3 mRNA and protein expression. PFKFB3 overexpression inhibited differentiation of keratinocytes while knockdown inhibited proliferation and increased the rate of differentiation. Furthermore, we found that PFKFB3 was highly expressed in psoriatic epidermis. Our results reveal that PFKFB3 is a key regulator of epidermal homeostasis and may represent a therapeutic target for epidermal diseases associated with hyperproliferation and impaired differentiation.

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          Author and article information

          Journal
          0426720
          4839
          J Invest Dermatol
          J. Invest. Dermatol.
          The Journal of investigative dermatology
          0022-202X
          1523-1747
          17 March 2017
          17 January 2017
          June 2017
          01 June 2018
          : 137
          : 6
          : 1267-1276
          Affiliations
          [1 ]Section of Pulmonary and Critical Care Medicine, Department of Medicine, Pritzker School of Medicine, The University of Chicago, Chicago, IL 60637, USA
          Author notes
          [* ]Corresponding author: Robert B. Hamanaka, PhD, 5841 S. Maryland Avenue, MC6026, Chicago, IL 60637 USA, Tel: +1-773-834-9829, Fax: +1-773-702-6500, rhamanaka@ 123456medicine.bsd.uchicago.edu
          Article
          PMC5441935 PMC5441935 5441935 nihpa859505
          10.1016/j.jid.2016.12.020
          5441935
          28108301
          f0e7a563-737e-43fa-9552-192da742049b
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