首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Anastrozole and RU486: Effects on estrogen receptor α and Mucin 1 expression and correlation in the MCF-7 breast cancer cell line
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Anastrozole and RU486: Effects on estrogen receptor α and Mucin 1 expression and correlation in the MCF-7 breast cancer cell line

机译:阿那曲唑和RU486:对MCF-7乳腺癌细胞系中雌激素受体α和粘蛋白1表达及相关性的影响

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摘要

Anastrozole and RU486 are shown to reduce hormone-responsive breast cancer progression when used as adjuvant treatments to surgical intervention, however, a high incidence of cancer recurrence remains. Estrogen receptor alpha (ERα) and Mucin 1 (MUC1), a glycoprotein, are both implicated in breast cancer progression. We assessed whether Anastrozole and RU486 treatment affects the expression of, and relationship between, ERα and MUC1 in the ERα+ MUC1+ MCF-7 breast cancer cell line. MCF-7 cells, treated with physiological concentrations of either Anastrozole or RU486 for 18h or 72h, were subjected to immunolocalization of both markers. CellProfiler software was used to quantify intensity for statistical analyses. ERα expression increased at both time periods following treatment. MUC1 expression increased with RU486-treatment at both times, whereas Anastrozole induced increased MUC1 expression at 72h only. The biomarkers demonstrated increased point association at 72h within treatment groups despite MUC1 diverging from correlation with ERα. We propose that tumor progression is independent of MUC1 and ERα correlation. These preliminary results indicate that withdrawal of adjuvant treatment may result in residual cell populations expressing increased ERα and MUC1. This phenotype may allow enhanced estrogenic and metastatic capacity influencing cancer recurrence, a hypothesis we are investigating further.
机译:当用作手术干预的辅助治疗方法时,阿那曲唑和RU486可以减少激素反应性乳腺癌的进展,但是,癌症复发的可能性仍然很高。雌激素受体α(ERα)和糖蛋白粘蛋白1(MUC1)均与乳腺癌的进展有关。我们评估了阿那曲唑和RU486治疗是否会影响ERα+ MUC1 + MCF-7乳腺癌细胞系中ERα和MUC1的表达及其之间的关系。用生理浓度的阿那曲唑或RU486处理MCF-7细胞18h或72h,对两种标记物进行免疫定位。使用CellProfiler软件量化强度以进行统计分析。 ERα表达在治疗后的两个时间段均增加。 RU486处理均使MUC1表达增加,而阿那曲唑仅在72h诱导MUC1表达增加。尽管MUC1与ERα的相关性不同,但生物标记物显示治疗组在72小时时的点相关性增加。我们建议肿瘤的进展独立于MUC1和ERα相关性。这些初步结果表明,停止辅助治疗可能会导致残留细胞群体表达增加的ERα和MUC1。这种表型可能会增强雌激素和转移能力,从而影响癌症的复发,我们正在进一步研究这一假设。

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