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Letter to the Editor| Volume 99, ISSUE 1, P69-72, July 2020

Selective PPARα agonist pemafibrate inhibits TNF-α-induced S100A7 upregulation in keratinocytes

  • Ayako Yumine
    Affiliations
    Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
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  • Gaku Tsuji
    Affiliations
    Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan

    Research and Clinical Center for Yusho and Dioxin, Kyushu University Hospital, Fukuoka, Japan
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  • Masutaka Furue
    Correspondence
    Corresponding author at: Graduate School of Medical Sciences, Kyushu University Maidashi 3-1-1, Higashi-ku, Fukuoka, 812-8582, Japan.
    Affiliations
    Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan

    Research and Clinical Center for Yusho and Dioxin, Kyushu University Hospital, Fukuoka, Japan

    Division of Skin Surface Sensing, Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
    Search for articles by this author
      The S100A protein family is a group of EF-hand-type calcium-binding proteins encoded by genes located in the epidermal differentiation complex that regulates cell structure, proliferation, and differentiation [
      • Leśniak W.
      • Graczyk-Jarzynka A.
      The S100 proteins in epidermis: topology and function.
      ]. Increased expression of S100A7, also named psoriasin, was first identified in psoriasis and is known as a useful marker of its disease activity [
      • D’Amico F.
      • Trovato C.
      • Skarmoutsou E.
      • Rossi G.A.
      • Granata M.
      • Longo V.
      • Gangemi P.
      • Pettinato M.
      • Mazzarino M.C.
      Effects of adalimumab, etanercept and ustekinumab on the expression of psoriasin (S100A7) in psoriatic skin.
      ,
      • D’Amico F.
      • Skarmoutsou E.
      • Granata M.
      • Trovato C.
      • Rossi G.A.
      • Mazzarino M.C.
      S100A7: a rAMPing up AMP molecule in psoriasis.
      ,
      • Sato Y.
      • Kajihara I.
      • Yamada-Kanazawa S.
      • Jinnin M.
      • Ihn H.
      S100A7 expression levels in coordination with interleukin-8 indicate the clinical response to infliximab for psoriasis patients.
      ]. S100A7 works as an antimicrobial peptide, chemoattracts immune cells including neutrophils, and accelerates local inflammation [
      • D’Amico F.
      • Skarmoutsou E.
      • Granata M.
      • Trovato C.
      • Rossi G.A.
      • Mazzarino M.C.
      S100A7: a rAMPing up AMP molecule in psoriasis.
      ]. The expression of S100A7 is upregulated by various proinflammatory cytokines including tumor necrosis factor-α (TNF-α) [
      • D’Amico F.
      • Skarmoutsou E.
      • Granata M.
      • Trovato C.
      • Rossi G.A.
      • Mazzarino M.C.
      S100A7: a rAMPing up AMP molecule in psoriasis.
      ]. Biological treatments such as the anti-TNF-α antibodies adalimumab and infliximab successfully reduce the lesional expression of S100A7 in psoriasis [
      • D’Amico F.
      • Trovato C.
      • Skarmoutsou E.
      • Rossi G.A.
      • Granata M.
      • Longo V.
      • Gangemi P.
      • Pettinato M.
      • Mazzarino M.C.
      Effects of adalimumab, etanercept and ustekinumab on the expression of psoriasin (S100A7) in psoriatic skin.
      ,
      • Sato Y.
      • Kajihara I.
      • Yamada-Kanazawa S.
      • Jinnin M.
      • Ihn H.
      S100A7 expression levels in coordination with interleukin-8 indicate the clinical response to infliximab for psoriasis patients.
      ].
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