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Yonsei Medical Journal ; : 708-716, 2010.
Article Dans Anglais | WPRIM | ID: wpr-53355

Résumé

PURPOSE: Oral squamous carcinoma (OSCC) cells exhibit resistance to chemotherapeutic agent-mediated apoptosis in the late stage of malignancy. Increased levels of heat shock proteins 70 (HSP70) in cancer cells are known to confer resistance to apoptosis. Since recent advances in the understanding of bacterial toxins have produced new strategies for the treatment of cancers, we investigated the effect of Pseudomonas aeruginosa exotoxin A (PEA) on HSP70 expression and induction of apoptosis in chemoresistant OSCC cell line (YD-9). MATERIALS AND METHODS: The apoptotic effect of PEA on chemoresistant YD-9 cells was confirmed by MTT, Hoechst and TUNEL stains, DNA electrophoresis, and Western blot analysis. RESULTS: While YD-9 cells showed high resistance to chemotherapeutic agents such as etoposide and 5-fluorouraci (5-FU), HSP70 antisense oligonucelotides sensitized chemoresistant YD-9 cells to etoposide and 5-FU. On the other hand, PEA significantly decreased the viability of YD-9 cells by deteriorating the HSP70-relating protecting system through inhibition of HSP70 expression and inducing apoptosis in YD-9 cells. Apoptotic manifestations were evidenced by changes in nuclear morphology, generation of DNA fragmentation, and activation of caspases. While p53, p21, and E2F-1 were upregulated, cdk2 and cyclin B were downregulated by PEA treatment, suggesting that PEA caused cell cycle arrest at the G2/M checkpoint. CONCLUSION: Therefore, these results indicate that PEA reduced the chemoresistance through inhibition of HSP70 expression and also induced apoptosis in chemoresistant YD-9 cells.


Sujets)
Humains , ADP ribose transferases/pharmacologie , Antinéoplasiques/pharmacologie , Apoptose/effets des médicaments et des substances chimiques , Toxines bactériennes/pharmacologie , Technique de Western , Carcinome épidermoïde/traitement médicamenteux , Cycle cellulaire/effets des médicaments et des substances chimiques , Lignée cellulaire tumorale , Chromatographie en phase liquide , Cycline B/métabolisme , Kinase-2 cycline-dépendante/métabolisme , Résistance aux médicaments antinéoplasiques/effets des médicaments et des substances chimiques , Facteur de transcription E2F1/métabolisme , Électrophorèse , Exotoxines/pharmacologie , Protéines du choc thermique HSP70/génétique , Méthode TUNEL , Tumeurs de la bouche/traitement médicamenteux , Spectrométrie de masse en tandem , Protéine p53 suppresseur de tumeur/métabolisme , Facteurs de virulence/pharmacologie
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