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.
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Authors | Jerome Terrasson, Bo Xu, Min Li, Sophie Allart, Jean-Luc Davignon, Li-he Zhang, Kui Wang, Christian Davrinche |
Journal | Fundamental & clinical pharmacology
(Fundam Clin Pharmacol)
Vol. 21
Issue 3
Pg. 281-9
(Jun 2007)
ISSN: 0767-3981 [Print] England |
PMID | 17521297
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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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
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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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