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Long-term exposure to estrogen enhances chemotherapeutic efficacy potentially through epigenetic mechanism in human breast cancer cells

机译:长期暴露于雌激素可能通过表观遗传机制增强人乳腺癌细胞的化学治疗功效

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摘要

Chemotherapy is the most common clinical option for treatment of breast cancer. However, the efficacy of chemotherapy depends on the age of breast cancer patients. Breast tissues are estrogen responsive and the levels of ovarian estrogen vary among the breast cancer patients primarily between pre- and post-menopausal age. Whether this age-dependent variation in estrogen levels influences the chemotherapeutic efficacy in breast cancer patients is not known. Therefore, the objective of this study was to evaluate the effects of natural estrogen 17 beta-estradiol (E2) on the efficacy of chemotherapeutic drugs in breast cancer cells. Estrogen responsive MCF-7 and T47D breast cancer cells were long-term exposed to 100 pg/ml estrogen, and using these cells the efficacy of chemotherapeutic drugs doxorubicin and cisplatin were determined. The result of cell viability and cell cycle analysis revealed increased sensitivities of doxorubicin and cisplatin in estrogen-exposed MCF-7 and T47D cells as compared to their respective control cells. Gene expression analysis of cell cycle, anti-apoptosis, DNA repair, and drug transporter genes further confirmed the increased efficacy of chemotherapeutic drugs in estrogen-exposed cells at molecular level. To further understand the role of epigenetic mechanism in enhanced chemotherapeutic efficacy by estrogen, cells were pre-treated with epigenetic drugs, 5-aza-2-deoxycytidine and Trichostatin A prior to doxorubicin and cisplatin treatments. The 5-aza-2 deoxycytidine pre-treatment significantly decreased the estrogen-induced efficacy of doxorubicin and cisplatin, suggesting the role of estrogen-induced hypermethylation in enhanced sensitivity of these drugs in estrogen-exposed cells. In summary, the results of this study revealed that sensitivity to chemotherapy depends on the levels of estrogen in breast cancer cells. Findings of this study will have clinical implications in selecting the chemotherapy strategies for treatment of breast cancer patients depending on the serum estrogen levels that varies among pre- and post-menopausal age of the patients.
机译:化学疗法是治疗乳腺癌的最常见的临床选择。但是,化学疗法的疗效取决于乳腺癌患者的年龄。乳腺癌组织对雌激素有反应,并且乳腺癌患者之间的卵巢雌激素水平主要在绝经前和绝经后之间有所不同。雌激素水平的这种年龄依赖性变化是否影响乳腺癌患者的化学治疗功效尚不清楚。因此,本研究的目的是评估天然雌激素17β-雌二醇(E2)对乳腺癌细胞中化疗药物功效的影响。将雌激素反应性MCF-7和T47D乳腺癌细胞长期暴露于100 pg / ml雌激素中,并使用这些细胞确定化疗药物阿霉素和顺铂的疗效。细胞活力和细胞周期分析的结果表明,与暴露于雌激素的MCF-7和T47D细胞相比,阿霉素和顺铂的敏感性分别高于对照细胞。细胞周期,抗凋亡,DNA修复和药物转运蛋白基因的基因表达分析进一步证实了化学治疗药物在暴露于雌激素的细胞中分子水平上的功效增强。为了进一步了解表观遗传机制在雌激素增强化学治疗功效中的作用,在用阿霉素和顺铂治疗之前,先用表观遗传药物,5-氮杂-2-脱氧胞苷和曲古他汀A预处理细胞。 5-氮杂-2脱氧胞苷预处理显着降低了雌激素诱导的阿霉素和顺铂的疗效,表明雌激素诱导的高甲基化在这些药物暴露于雌激素的细胞中的敏感性增强中的作用。总之,这项研究的结果表明对化疗的敏感性取决于乳腺癌细胞中雌激素的水平。这项研究的结果将在根据乳腺癌绝经前后年龄不同的血清雌激素水平选择化疗策略治疗乳腺癌患者中具有临床意义。

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