Tamoxifen and tranilast show a synergistic effect against breast cancer in vitro.
Bratisl Lek Listy
; 116(1): 69-73, 2015.
Article
en En
| MEDLINE
| ID: mdl-25666966
ABSTRACT
OBJECTIVE:
This study was aimed at examining a separate or combined effect of tamoxifen and tranilast drugs on growth and proliferation of breast cancer cells.BACKGROUND:
Breast cancer is one of the most common cancers and the second leading cause of cancer death among women worldwide. Tamoxifen is the most widely used anti-estrogen for the treatment of breast cancer. Studies show that a combination therapy with other drugs enhances the activity of tamoxifen. Tranilast is an anti-inflammatory drug. We hypothesize that tranilast plus tamoxifen can work synergistically and help getting better result from this anticancer drug.METHODS:
Two breast cancer cell lines, MCF-7 and MDA-MB-231, were treated with graduated concentrations of tamoxifen and tranilast alone or in combination at 24, 48 or 72 hours for MCF-7, and 48 hours for MDA-MB-231 cells. We used the MTT assay and lactate dehydrogenase leakage (LDH) assay to evaluate cell viability and cytotoxicity, respectively.RESULTS:
In both ER-positive and ER-negative breast cancer cell lines, the combination of tranilast and tamoxifen was more effective in growth inhibition than single drug exposure.CONCLUSION:
We have demonstrated that by means of a synergistic/additive inhibitory effect, tranilast was capable of enhancing the in vitro activity of tamoxifen on breast cancer cell lines. Based on the results obtained in this study, tranilast could be a candidate drug for combination therapy in resistant breast cancer patients (Fig. 9, Ref. 17). KEYWORDS breast cancer, Tamoxifen, Tranilast, LDH release, MTT.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Tamoxifeno
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Neoplasias de la Mama
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Protocolos de Quimioterapia Combinada Antineoplásica
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Antiinflamatorios no Esteroideos
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Antineoplásicos Hormonales
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Ortoaminobenzoatos
Límite:
Female
/
Humans
Idioma:
En
Revista:
Bratisl Lek Listy
Año:
2015
Tipo del documento:
Article