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Blockade of epidermal growth factor receptor/mammalian target of rapamycin pathway by Icariside II results in reduced cell proliferation of osteosarcoma cells.

Abstract
Icariside II is considered one of the most important natural flavonoids with multiple bioactivities from traditional Chinese medicine Yin Yanghuo (YYH) or Horny Goat Weed (Epimedium koreanum Nakai). Previous studies show that Icariside II exhibits potent cytotoxicity against a broad spectrum of human cancer cells through various signaling transduction pathways. However, there are few reports about the effect of Icariside II on osteosarcoma cell. In this study, we found that Icariside II decreased cell proliferation in human osteosarcoma MG-63 cells and human osteosarcoma Saos-2 cells. In addition, Icariside II inactivated EGFR/mTOR signaling pathway, including EGFR, PI3K/AKT/PRAS40, Raf/MEK/ERK as well as mTOR. Furthermore, Icariside II inhibited epidermal growth factor (EGF)-induced activation of EGFR/mTOR signaling pathway. Pretreatment of EGF partially reversed cell viability decreased by Icariside II. Importantly, Icariside II inhibited the proliferation of transplantable tumors and EGFR/mTOR signaling pathway in sarcoma-180 bearing mice. In summary, these results indicate that Icariside II inhibits the proliferation of osteosarcoma cells in vitro and in vivo via EGFR/mTOR signaling pathway.
AuthorsYa-di Geng, Lei Yang, Chao Zhang, Ling-Yi Kong
JournalFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association (Food Chem Toxicol) Vol. 73 Pg. 7-16 (Nov 2014) ISSN: 1873-6351 [Electronic] England
PMID25119583 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 Elsevier Ltd. All rights reserved.
Chemical References
  • Flavonoids
  • baohuoside I
  • MTOR protein, human
  • ErbB Receptors
  • TOR Serine-Threonine Kinases
Topics
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • ErbB Receptors (antagonists & inhibitors, metabolism)
  • Flavonoids (pharmacology)
  • Humans
  • Osteosarcoma (metabolism, pathology)
  • Signal Transduction
  • TOR Serine-Threonine Kinases (antagonists & inhibitors, metabolism)

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