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Photodynamic therapy inhibits melanogenesis through paracrine effects by keratinocytes and fibroblasts.

Abstract
Photodynamic therapy (PDT) is a treatment option for skin cancer and premalignant skin diseases and exhibits rejuvenation effects, including reducing fine wrinkles and whitening, on aged skin. In this study, we investigated the mechanism underlying the whitening effects of PDT on melanocytes (MCs) in vitro and in vivo. Exposure of MCs to PDT in vitro reduced their melanin content and tyrosinase activity without, however, affecting cell survival. Interestingly, melanogenesis was also inhibited by exposing MCs to conditioned media of PDT-treated keratinocytes or dermal fibroblasts. This paracrine effect was likely due to a decreased release of melanocyte-stimulating cytokines such as Kit ligand and hepatocyte growth factor from these cells. Furthermore, we observed that PDT reduced mottled hyperpigmentation of photoaged patient skin in vivo, highlighting the clinical importance of skin whitening by PDT.
AuthorsSue Kyung Kim, Seung-Jae Oh, Se-Yeon Park, Woo-Jung Kim, You-Sun Kim, You Chan Kim
JournalPigment cell & melanoma research (Pigment Cell Melanoma Res) Vol. 31 Issue 2 Pg. 277-286 (03 2018) ISSN: 1755-148X [Electronic] England
PMID29045012 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Chemical References
  • Culture Media, Conditioned
  • Cytokines
  • Melanins
  • Microphthalmia-Associated Transcription Factor
  • Monophenol Monooxygenase
  • Extracellular Signal-Regulated MAP Kinases
Topics
  • Animals
  • Cattle
  • Culture Media, Conditioned (pharmacology)
  • Cytokines (metabolism)
  • Extracellular Signal-Regulated MAP Kinases (metabolism)
  • Fibroblasts (metabolism)
  • Humans
  • Hyperpigmentation (metabolism)
  • Infant, Newborn
  • Keratinocytes (drug effects, metabolism)
  • Melanins (biosynthesis)
  • Melanocytes (drug effects, enzymology)
  • Microphthalmia-Associated Transcription Factor (metabolism)
  • Monophenol Monooxygenase (metabolism)
  • Paracrine Communication (drug effects)
  • Phosphorylation (drug effects)
  • Photochemotherapy
  • Skin (pathology)

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