Abstract |
To determine the synergy of 5-aza-2'-deoxycytidine (DAC) and paclitaxel (PTX) against prostate carcinoma (PC) cells by isobolographic analysis. We demonstrated that DAC could significantly increase the susceptibility of PC cells to PTX, and confirmed the synergy of DAC and PTX. DAC enhanced the PTX induced up-regulation of caspase activity and antiproliferative effect, resulting in an increase of cells in subG1 and G2/M phases. In addition, the synergy was observed in both androgen-dependent and -independent PC cell lines. It suggested that combination chemotherapy with DAC and PTX might be a new strategy to improve the clinical response rate of PC.
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Authors | Donghao Shang, Yuting Liu, Qingjun Liu, Fengbo Zhang, Lang Feng, Wencheng Lv, Ye Tian |
Journal | Cancer letters
(Cancer Lett)
Vol. 278
Issue 1
Pg. 82-7
(Jun 08 2009)
ISSN: 1872-7980 [Electronic] Ireland |
PMID | 19168279
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium
- Androgens
- Antineoplastic Agents, Phytogenic
- Tetrazolium Salts
- Decitabine
- Oxidoreductases
- Caspases
- Azacitidine
- Paclitaxel
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Topics |
- Androgens
(physiology)
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Apoptosis
(drug effects)
- Azacitidine
(analogs & derivatives, pharmacology, therapeutic use)
- Caspases
(metabolism)
- Cell Cycle
(drug effects)
- Cell Division
(drug effects)
- Cell Line, Tumor
- Decitabine
- Flow Cytometry
- Humans
- Male
- Mitochondria
(enzymology)
- Oxidoreductases
(metabolism)
- Paclitaxel
(pharmacology, therapeutic use)
- Prostatic Neoplasms
(drug therapy, enzymology, pathology)
- Tetrazolium Salts
(metabolism)
- Up-Regulation
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