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Activities of Z-ajoene against tumour and viral spreading in vitro.

Abstract
Z-ajoene is a garlic-derived compound with known anti-tumour properties. This report argues in favour of pro-apoptotic and cell cycle blockage activities of Z-ajoene on various cell lines involving activation of the p53-family gene products, p53, p63 and p73, at indicated doses. According to its known anti-proteasome activity, Z-ajoene induced a downregulation of MHC-class I expression at the surface of treated cells but did not impair their recognition by CD8+ T cells. We further demonstrated a new activity of Z-ajoene against human cytomegalovirus spreading in vitro that was mediated by an increased number of apoptotic cells after infection. Altogether our data point at the ubiquitous efficiency of Z-ajoene as a new compound to fight against cancers of various origins including those that put up viruses.
AuthorsJerome Terrasson, Bo Xu, Min Li, Sophie Allart, Jean-Luc Davignon, Li-he Zhang, Kui Wang, Christian Davrinche
JournalFundamental & clinical pharmacology (Fundam Clin Pharmacol) Vol. 21 Issue 3 Pg. 281-9 (Jun 2007) ISSN: 0767-3981 [Print] England
PMID17521297 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Disulfides
  • HLA-A2 Antigen
  • Nuclear Proteins
  • RNA, Messenger
  • Sulfoxides
  • TP63 protein, human
  • TP73 protein, human
  • Trans-Activators
  • Transcription Factors
  • Tumor Protein p73
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • ajoene
  • Proteasome Endopeptidase Complex
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • CD8-Positive T-Lymphocytes (drug effects, immunology)
  • Cell Line, Tumor
  • Cytomegalovirus (drug effects, physiology)
  • DNA-Binding Proteins (genetics, metabolism)
  • Disulfides (pharmacology)
  • Fibroblasts (drug effects, virology)
  • Genes, MHC Class I (physiology)
  • HLA-A2 Antigen (metabolism)
  • Humans
  • Nuclear Proteins (genetics, metabolism)
  • Proteasome Endopeptidase Complex (metabolism)
  • RNA, Messenger (metabolism)
  • Sulfoxides
  • Trans-Activators (genetics, metabolism)
  • Transcription Factors
  • Tumor Protein p73
  • Tumor Suppressor Protein p53 (genetics, metabolism)
  • Tumor Suppressor Proteins (genetics, metabolism)

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