Docetaxel/Zoledronic Acid Combination Triggers Apoptosis Synergistically Through Downregulating Antiapoptotic Bcl-2 Protein Level in Hormone-Refractory Prostate Cancer Cells
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Open Access Color
BRONZE
Green Open Access
Yes
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Publicly Funded
No
Abstract
Docetaxel, a semi-synthetic taxane analogue, is used effectively in the treatment of metastatic prostate cancer. Zoledronic acid, the most potent member of bisphosphonates, has shown pleiotropic anti-tumoral effects on prostate cancer cells. We have explored the possible additive/synergistic effects and the apoptotic pathways induced by combination treatment of docetaxel and zoledronic acid in hormone and drug refractory, PC-3 and DU-145 prostate cancer cells. Combination of docetaxel and zoledronic acid synergistically inhibits cell growth in PC-3 and DU-145 cells. Moreover, this effect was due to downregulation of antiapoptotic protein Bcl-2 in PC-3 and DU-145 cells. In conclusion, docetaxel/zoledronic acid combination is potentially a novel and effective approach for the treatment of prostate cancer.
Description
Keywords
Zoledronic acid, Prostate cancer, Docetaxel, Bcl-2, DU-145, PC-3, Male, Down-Regulation, Antineoplastic Agents, Apoptosis, DNA Fragmentation, Docetaxel, Zoledronic Acid, PC-3, Cell Line, Tumor, Humans, Bcl-2, DU-145, Zoledronic acid, Caspase 7, Prostate cancer, Diphosphonates, Caspase 3, Imidazoles, Prostatic Neoplasms, Drug Synergism, Proto-Oncogene Proteins c-bcl-2, Drug Resistance, Neoplasm, Androgens, Taxoids
Fields of Science
03 medical and health sciences, 0302 clinical medicine
Citation
Karabulut, B., Erten, C., Gül, M. K., Cengiz, E., Karaca, B., Küçükzeybek, Y., Görümlü, G., Atmaca, H., Uzunoğlu, S., Şanlı, U. A., Baran, Y., and Uslu, R. (2009). Docetaxel/zoledronic acid combination triggers apoptosis synergistically through downregulating antiapoptotic Bcl-2 protein level in hormone-refractory prostate cancer cells. Cell Biology International, 33(2), 239-246. doi:10.1016/j.cellbi.2008.11.011
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OpenCitations Citation Count
39
Volume
33
Issue
2
Start Page
239
End Page
246
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CrossRef : 34
Scopus : 47
PubMed : 16
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