Abstract | OBJECTIVES/HYPOTHESIS: METHODS:
HNSCC cells (HN30 and HN12) were exposed to either XRP6258 or docetaxel. XRP6258-induced growth suppression, cell cycle arrest and apoptosis were measured. Further, XRP6258-induced expression patterns of selected genes were compared to docetaxel-induced expression patterns using Western blot analysis. RESULTS:
XRP6258 suppressed proliferation and induced G(2)M arrest and apoptosis in both of the cell lines tested. XRP6258 and docetaxel produced similar alteration in the expression of cell cycle regulators, such as cyclin A and cyclin B1. The expression of E2F and EGFR were decreased in both XRP6258 and docetaxel-treated HNSCC cells. Finally, XRP6258 induced a greater level of bcl2 phosphorylation than docetaxel in HN12 cell line. CONCLUSIONS:
XRP6258 appeared to have a similar mechanism of action as docetaxel in the two HNSCC cell lines studied. XRP6258 induced cell cycle arrest, growth suppression, and apoptosis by altering gene expression patterns similar to that induced by docetaxel. These preclinical experiments suggest that XRP6258 may be useful in treating HNSCC, and the aforementioned genes can potentially be used as surrogate endpoint biomarkers.
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Authors | George H Yoo, Zyed Kafri, John F Ensley, Fulvio Lonardo, Harold Kim, Adam J Folbe, Joshua Won, Timothy Stevens, Ho-Sheng Lin |
Journal | The Laryngoscope
(Laryngoscope)
Vol. 120
Issue 6
Pg. 1114-9
(Jun 2010)
ISSN: 1531-4995 [Electronic] United States |
PMID | 20513026
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Annexin A5
- Cyclin A
- Cyclin B1
- Taxoids
- XRP6258
- Docetaxel
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Topics |
- Annexin A5
(metabolism)
- Apoptosis
(drug effects, genetics)
- Blotting, Western
- Carcinoma, Squamous Cell
(drug therapy, genetics)
- Cell Cycle
(drug effects, genetics)
- Cell Line, Tumor
- Cyclin A
(metabolism)
- Cyclin B1
(metabolism)
- Docetaxel
- Gene Expression Profiling
- Gene Expression Regulation, Neoplastic
(drug effects)
- Head and Neck Neoplasms
(drug therapy, genetics)
- Humans
- Phosphorylation
- Taxoids
(pharmacology)
- Tumor Cells, Cultured
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