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Merck
CN
  • Reversal of ER-β silencing by chromatin modifying agents overrides acquired tamoxifen resistance.

Reversal of ER-β silencing by chromatin modifying agents overrides acquired tamoxifen resistance.

Cancer letters (2013-06-12)
Chara A Pitta, Panagiotis Papageorgis, Christiana Charalambous, Andreas I Constantinou
摘要

The purpose of this work is to determine the molecular mechanisms underlying tamoxifen resistance. We show here that ER-β is epigenetically silenced in a cell line with acquired tamoxifen resistance (MCF-7/TAM-R) and this could be reversed by 5-AZA-deoxycytidine (5-AZA) and trichostatin-A (TSA) pre-treatment. Subsequent treatment with 4-hydroxy-tamoxifen (4-OHT) induced ER-β nuclear translocation, upregulated pS2 and p21 levels and reduced cell viability. Transfection with an ER-β expression vector sensitized MCF-7/TAM-R cells to the growth inhibitory and pro-apoptotic effects of 4-OHT, indicating that ER-β re-expression alone is sufficient to restore sensitivity to tamoxifen. This novel finding reveals that ER-β is fundamental in overcoming acquired tamoxifen resistance and provides insights for new therapeutic protocols against breast cancer.

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Sigma-Aldrich
4-羟基他莫西芬, ≥70% Z isomer (remainder primarily E-isomer)
Supelco
4-羟基他莫西芬, analytical standard, (E) and (Z) isomers (50:50)