Papers

Peer-reviewed
Oct, 2014

Synthetic (+)-terrein suppresses interleukin-6/soluble interleukin-6 receptor induced-secretion of vascular endothelial growth factor in human gingival fibroblasts

BIOORGANIC & MEDICINAL CHEMISTRY
  • Hiroki Mandai
  • Kazuhiro Omori
  • Daisuke Yamamoto
  • Toki Tsumura
  • Kyouta Murota
  • Satoshi Yamamoto
  • Koichi Mitsudo
  • Soichiro Ibaragi
  • Akira Sasaki
  • Hiroshi Maeda
  • Shogo Takashiba
  • Seiji Suga
  • Display all

Volume
22
Number
19
First page
5338
Last page
5344
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.bmc.2014.07.047
Publisher
PERGAMON-ELSEVIER SCIENCE LTD

Interleukin (IL)-6 is a proinflammatory cytokine that performs a wide variety of biological functions, including important roles in the progression of chronic inflammatory diseases such as periodontal disease. (+)-Terrein, a secondary bioactive fungal metabolite isolated from Aspergillus terreus, has various biological activities; however, its anti-inflammatory effects are still unknown. The purpose of this study was to examine the effect of synthetic (+)-terrein on IL-6 signaling and related protein production in human gingival fibroblasts. To our knowledge, this study is the first to report that synthetic (+)-terrein is not cytotoxic at concentrations less than 20 mu M and suppresses IL-6/soluble IL-6 receptor (sIL-6R)-induced phosphorylation of signal transducer and activator of transcription-3, extracellular signal-regulated kinase 1/2, and c-jun N-terminal kinase 1/2-signaling proteins that are downstream of IL-6 signaling. In addition, synthetic (+)-terrein suppresses IL-6/sIL-6R-induced vascular endothelial growth factor (VEGF) secretion in a concentration-dependent manner (p < 0.01). These data suggest that synthetic (+)-terrein has potential anti-IL-6 signaling activity and suppresses VEGF-associated inflammatory disease progression. (C) 2014 Elsevier Ltd. All rights reserved.

Link information
DOI
https://doi.org/10.1016/j.bmc.2014.07.047
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/25151086
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000341883700020&DestApp=WOS_CPL
ID information
  • DOI : 10.1016/j.bmc.2014.07.047
  • ISSN : 0968-0896
  • eISSN : 1464-3391
  • Pubmed ID : 25151086
  • Web of Science ID : WOS:000341883700020

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