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MicroRNA expression analysis of human skin fibroblasts treated with high-fluence light-emitting diode-red light.

Abstract
Skin fibrosis is a chronic debilitating feature of several skin diseases that lead to characteristic increases in dermal fibroblast proliferation and collagen deposition through upregulation in components of the transforming growth factor beta (TGF-B)/SMAD pathway. In contrast to ultraviolet phototherapy, high-fluence light-emitting diode-generated red light (HF-LED-RL, 633 ± 15 nm) is a safe, economic and non-invasive therapy with in vitro evidence that supports modulation of the key cellular characteristics involved in the pathogenesis of skin fibrosis. Limited data exists pertaining to the effects of HF-LED-RL on human skin fibroblast microRNA (miRNA). Herein, we explored the effects of HF-LED-RL on fibroblast miRNA levels using RNA-seq and miRNA expression analysis. Using RNA-seq analysis we found that HF-LED-RL at 320 and 640 J/cm2 increased transcription of key miRNA that are involved in skin fibrosis including miRNA-29, miRNA-196a and Let-7a, and decreased transcription of miRNA-21, miRNA-23b and miRNA-31. These microRNA findings provide insight into the molecular underpinnings of HF-LED-RL and highlight potential therapeutic targets of interest for the treatment of skin fibrosis. Additional research on the specific molecular mechanisms underlying HF-LED-RL effects on fibroblasts may provide further mechanistic insight into this therapy and may reveal additional future therapeutic targets for skin fibrosis.
AuthorsAndrew Mamalis, Eugene Koo, Clifford Tepper, Jared Jagdeo
JournalJournal of biophotonics (J Biophotonics) Vol. 12 Issue 5 Pg. e201800207 (05 2019) ISSN: 1864-0648 [Electronic] Germany
PMID30182520 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Chemical References
  • MicroRNAs
Topics
  • Fibroblasts (metabolism, radiation effects)
  • Humans
  • Light
  • MicroRNAs (genetics)
  • Phototherapy
  • Skin (cytology)
  • Transcriptome (radiation effects)

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