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Vanillin suppresses in vitro invasion and in vivo metastasis of mouse breast cancer cells.

Abstract
Vanillin, a food flavoring agent, has been reported to show anti-mutagenic activity and to inhibit chemical carcinogenesis. In this study, we examined the effect of vanillin on the growth and metastasis of 4T1 mammary adenocarcinoma cells in BALB/c mice. Mice orally administered with vanillin showed significantly reduced numbers of lung metastasized colonies compared to controls. In vitro studies revealed that vanillin, at concentrations that were not cytotoxic, inhibited invasion and migration of cancer cells and inhibited enzymatic activity of MMP-9 secreted by the cancer cells. Vanillin also showed growth inhibitory effect towards cancer cells in vitro. However, vanillic acid, a major metabolic product of vanillin in human and rat, was not active in these in vitro activity assays. Our findings suggest that vanillin has anti-metastatic potential by decreasing invasiveness of cancer cells. Since vanillin is generally regarded as safe, it may be of value in the development of anti-metastatic drugs for cancer treatment.
AuthorsKriengsak Lirdprapamongkol, Hiroaki Sakurai, Noritaka Kawasaki, Min-Kyung Choo, Yurika Saitoh, Yasushi Aozuka, Pattama Singhirunnusorn, Somsak Ruchirawat, Jisnuson Svasti, Ikuo Saiki
JournalEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences (Eur J Pharm Sci) Vol. 25 Issue 1 Pg. 57-65 (May 2005) ISSN: 0928-0987 [Print] Netherlands
PMID15854801 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Benzaldehydes
  • vanillin
  • Matrix Metalloproteinase 9
Topics
  • Animals
  • Benzaldehydes (pharmacology)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Female
  • Mammary Neoplasms, Experimental (drug therapy, pathology)
  • Matrix Metalloproteinase 9 (metabolism)
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Structure-Activity Relationship

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