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The Comparison of The Effects of Silybin and Silybin-Phosphatidylcholine on Viability and ESR Expression in Human Breast Cancer T47D Cell Line.
Mahmoodi, Narges; Motamed, Nasrin; Paylakhi, Seyed Hassan.
Afiliación
  • Mahmoodi N; Department of Cell and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran ; School of Biology, University College of Science, University of Tehran, Tehran, Iran.
  • Motamed N; Department of Cell and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran ; School of Biology, University College of Science, University of Tehran, Tehran, Iran.
  • Paylakhi SH; School of Biology, Damghan University, Damghan, Iran.
Cell J ; 16(3): 299-308, 2014.
Article en En | MEDLINE | ID: mdl-24611152
OBJECTIVE: Silybin is a polyphenol with anti-oxidant and anti-cancer properties. The poor bioavailability of some polyphenols can be improved by binding to phosphatidylcholine. In recent years, studies have been conducted to evaluate the anti-cancer effect of silybin. We studied the effect of silybin and silybin-phosphatidylcholine on ESR1 and ESR2 gene expression and viability in the T47D breast cancer cell line. MATERIALS AND METHODS: In this experimental study, a 3-(4,5-Dimethylthiazol-2-Yl)-2,5-Diphenyltetrazolium Bromide test (MTT test) was used to determine doses for cell treatment, and the gene expression was analyzed by real-time reverse transcriptase-polymerase chain reaction (real-time RT- PCR). RESULTS: Significant dose- and time-dependent cell growth inhibitory effects of silybin and silybin-phosphatidylcholine along with ESR1 down-regulation were observed in T47D cells. In contrast to ESR1, the T47D cell line showed negligible ESR2 expression. CONCLUSION: This study suggests that silybin and silybin-phosphatidylcholine down-regulate ESR1 in ER(+)breast cancers. Results also show that in the T47D cell line, silybindown-regulation of ESR1 compared with silybin.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Cell J Año: 2014 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Cell J Año: 2014 Tipo del documento: Article País de afiliación: Irán