Abstract |
Effects of toremifene (TOR) in combination with paclitaxel (TXL) on various human breast cancer cell lines were evaluated. TOR and TXL exhibited additive effects on estrogen receptor (ER)-positive cancer cell lines, MCF-7 and T-47D, and a sub-additive effect on a tamoxifen (TAM)-resistant line, T-47D/TAM. To all three ER-negative cancer cell lines, the combined treatment also showed additive effects on MDA-MB-134VI, MDA-MB-231 and MDA-MB-453. Furthermore, a synergistic effect was observed on a multi- drug resistant (MDR) line, Adr. This synergistic effect was more potent in the combination with TOR than that with TAM. The combined treatment increased intracellular TXL, and the accumulation by TOR was 1.5-fold that by TAM. Consequently, the ratio of G2M arrested cells was higher, with statistical significance, in the TOR combination than in the TAM combination. In addition, these synergistic effects in MDR cells were also observed in the combination of TXL with major clinical active metabolites, N-desmethyl-TOR (TOR-1) and 4-hydroxy-TOR (TOR-2). These results suggest that the combination therapy of TOR and TXL might be an effective clinical treatment for breast cancer patients.
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Authors | Sakiko Maruyama, Shunsuke Kuroiwa, Atsuya Saimoto, Kiyohiro Nishikawa |
Journal | Gan to kagaku ryoho. Cancer & chemotherapy
(Gan To Kagaku Ryoho)
Vol. 30
Issue 5
Pg. 669-75
(May 2003)
ISSN: 0385-0684 [Print] Japan |
PMID | 12795099
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Selective Estrogen Receptor Modulators
- Toremifene
- Paclitaxel
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Topics |
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Breast Neoplasms
(pathology)
- Drug Synergism
- Humans
- Paclitaxel
(pharmacology)
- Selective Estrogen Receptor Modulators
(pharmacology)
- Toremifene
(pharmacology)
- Tumor Cells, Cultured
(drug effects)
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