Abstract |
The effects of the aromatase inhibitor, CGS16949A, and the fluoropyrimidine, 5-fluorouracil (5-FU), on cell cycle distribution and growth were studied using FACS analysis and MTT assay in the human breast cancer cell line, SK-BR-3. CGS16949A induced an increase in the G0-G1 fraction on SK-BR-3 cells, and the growth inhibition rate of the combination of both (65.7 +/- 3.0%) was significantly higher than 10 nM CGS16949A (37.9 +/- 6.9%) or 100 microg/ml 5-FU (45.6 +/- 4.5%); p < 0.01). Administering 5-FU after preincubation with CGS16949A significantly increased the combined cytotoxic efficacy, suggesting that clinical therapy using this combined therapy may be more efficient.
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Authors | Y Tsunoda, Y Shimizu, A Tsunoda, M Shibusawa, K Kamiya, M Kusano, K Fukuchi |
Journal | European surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes
(Eur Surg Res)
2001 May-Jun
Vol. 33
Issue 3
Pg. 232-6
ISSN: 0014-312X [Print] Switzerland |
PMID | 11490127
(Publication Type: Journal Article)
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Copyright | Copyright 2001 S. Karger AG, Basel |
Chemical References |
- Antimetabolites, Antineoplastic
- Antineoplastic Agents, Hormonal
- Aromatase
- Fadrozole
- Fluorouracil
|
Topics |
- Antimetabolites, Antineoplastic
(pharmacology)
- Antineoplastic Agents, Hormonal
(pharmacology)
- Aromatase
(metabolism)
- Breast Neoplasms
(enzymology, pathology)
- Cell Cycle
(drug effects)
- Dose-Response Relationship, Drug
- Drug Synergism
- Fadrozole
(pharmacology)
- Female
- Fluorouracil
(pharmacology)
- Humans
- Tumor Cells, Cultured
(drug effects)
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