Chang Yu-Wei, Singh Kamaleshwar P
Department of Environmental Toxicology, The Institute of Environmental and Human Health (TIEHH), Texas Tech University, Lubbock, Texas, United States of America.
PLoS One. 2017 Mar 21;12(3):e0174227. doi: 10.1371/journal.pone.0174227. eCollection 2017.
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.
化疗是治疗乳腺癌最常见的临床选择。然而,化疗的疗效取决于乳腺癌患者的年龄。乳腺组织对雌激素有反应,且乳腺癌患者中卵巢雌激素水平主要在绝经前和绝经后年龄段有所不同。雌激素水平的这种年龄依赖性变化是否会影响乳腺癌患者的化疗疗效尚不清楚。因此,本研究的目的是评估天然雌激素17β-雌二醇(E2)对乳腺癌细胞化疗药物疗效的影响。对雌激素反应性的MCF-7和T47D乳腺癌细胞长期暴露于100 pg/ml雌激素,并使用这些细胞测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结果显示,与各自的对照细胞相比,暴露于雌激素的MCF-7和T47D细胞对阿霉素和顺铂的敏感性增加。细胞周期、抗凋亡、DNA修复和药物转运基因的基因表达分析进一步在分子水平上证实了化疗药物在暴露于雌激素的细胞中的疗效增加。为了进一步了解表观遗传机制在雌激素增强化疗疗效中的作用,在阿霉素和顺铂治疗前,用表观遗传药物5-氮杂-2'-脱氧胞苷和曲古抑菌素A对细胞进行预处理。5-氮杂-2'-脱氧胞苷预处理显著降低了雌激素诱导的阿霉素和顺铂疗效,表明雌激素诱导的高甲基化在增强这些药物在暴露于雌激素的细胞中的敏感性方面发挥了作用。总之,本研究结果表明,对化疗的敏感性取决于乳腺癌细胞中的雌激素水平。本研究结果对于根据患者绝经前和绝经后血清雌激素水平的差异来选择乳腺癌患者的化疗策略具有临床意义。