Published September 23, 2005 | Version v1
Journal article

[6]-Gingerol, a pungent ingredient of ginger, inhibits angiogenesis in vitro and in vivo

  • 1. Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chunchon, Kangwon-Do (Korea, Republic of)
  • 2. Department of Biochemistry, College of Natural Sciences, Yonsei University, Seoul (Korea, Republic of)
  • 3. Laboratory of Dermatology-Immunology, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, Seoul (Korea, Republic of)
  • 4. Korea Institute of Science and Technology, 39-1 Hawolgok-dong, Seongbuk-gu, Seoul (Korea, Republic of)
  • 5. Vascular System Research Center, Kangwon National University, Chunchon, Kangwon-do (Korea, Republic of)

Description

[6]-Gingerol, a pungent ingredient of ginger (Zingiber officinale Roscoe, Zingiberaceae), has anti-bacterial, anti-inflammatory, and anti-tumor-promoting activities. Here, we describe its novel anti-angiogenic activity in vitro and in vivo. In vitro, [6]-gingerol inhibited both the VEGF- and bFGF-induced proliferation of human endothelial cells and caused cell cycle arrest in the G1 phase. It also blocked capillary-like tube formation by endothelial cells in response to VEGF, and strongly inhibited sprouting of endothelial cells in the rat aorta and formation of new blood vessel in the mouse cornea in response to VEGF. Moreover, i.p. administration, without reaching tumor cytotoxic blood levels, to mice receiving i.v. injection of B16F10 melanoma cells, reduced the number of lung metastasis, with preservation of apparently healthy behavior. Taken together, these results demonstrate that [6]-gingerol inhibits angiogenesis and may be useful in the treatment of tumors and other angiogenesis-dependent diseases

Additional details

Identifiers

DOI
10.1016/j.bbrc.2005.07.076;
PII
S0006-291X(05)01454-3;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
335
Journal Issue
2
Journal Page Range
p. 300-308
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.