11,11′-Dideoxy-verticillin: A natural compound possessing growth factor receptor tyrosine kinase-inhibitory effect with anti-tumor activity

Yi Xiang Zhang, Yi Chen, Xiao Ning Guo, Xiong Wen Zhang, Wei Min Zhao, Li Zhong, Jin Zhou, Yong Xi, Li Ping Lin, Jian Ding

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61 Scopus citations

Abstract

11,11′-Dideoxy-verticillin, a compound of the novel epidithiodioxopiprazine structural class, is isolated from the traditional Chinese medicinal herb Shiraia bambusicola. The present study demonstrated for the first time that 11,11′-dideoxy-verticillin has potent tyrosine kinase-inhibitory and anti-tumor activities. In the cell-free ELISA tyrosine kinase assay, 11,11′-dideoxy-verticillin significantly inhibited the activities of epidermal growth factor receptor (EGFR), vascular endothelial growth factor receptor-1/fms-like tyrosine kinase-1 (VEGFR-1/Flt-1) and human epidermal growth factor receptor-2 (HER2/ErbB-2), with relative specificity on EGFR and VEGFR-1 with IC50S of 0.136±0.109 and 1.645±0.885 nM, respectively. Exposure of 11,11′-dideoxy- verticillin for 1 h to EGFR-overexpressed MDA-MB-468 human breast carcinoma cells and HER2-overexpressed SK-OV-3 human ovarian adenocarcinoma cells resulted in obvious inhibition of EGF-induced phosphorylation of EGFR and HER2. In addition, 11,11′-dideoxy-verticillin also inhibited the EGF-induced phosphorylation of Erk1/2, but had no effect on the phosphorylation of AKT in both tumor cell lines. Moreover, 11,11′-dideoxy-verticillin has potent anti-tumor activity. In vitro cytotoxicity assay showed that 11,11′-dideoxy-verticillin potently inhibited the proliferation of four human breast tumor cell lines with an average IC50 value of 0.2 μM. In vivo, 11,11′-dideoxy-verticillin exhibited remarkable efficacy against mice sarcoma 180 and hepatoma 22 after daily i.p. administration of 0.5 or 0.75 mg/kg with inhibition rates ranging from 45.0 to 72.4%. Treated with 11,11′-dideoxy-verticillin at 0.5-2.0 μM for 36 h, MB-MB-468 cells exhibited significant apoptotic morphological changes. At low concentrations (0.0625-0.5 μM) for 24 h, 11,11′-dideoxy-verticillin induced a dose-dependent accumulation of MDA-MB-468 cells in the G2/M phase of the cell cycle. These results indicate that 11,11′-dideoxy-verticillin is a naturally derived growth factor receptor tyrosine kinase inhibitor with potent anti-tumor activity.

Original languageEnglish
Pages (from-to)515-524
Number of pages10
JournalAnti-Cancer Drugs
Volume16
Issue number5
DOIs
StatePublished - May 2005
Externally publishedYes

Keywords

  • 11,11′-dideoxy-verticillin
  • Anti-tumor
  • Epidermal growth factor receptor
  • Erk1/2
  • Vascular endothelial growth factor receptor-1

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