首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Muc1 -induced Alterations In A Lipid Metabolic Gene Network Predict Response Of Human Breast Cancers To Tamoxifen Treatment
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Muc1 -induced Alterations In A Lipid Metabolic Gene Network Predict Response Of Human Breast Cancers To Tamoxifen Treatment

机译:Muc1诱导的脂质代谢基因网络改变预测人类乳腺癌对他莫昔芬治疗的反应

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摘要

The mucin 1 (MUC1) oncoprotein is aberrantly overexpressed in human breast cancers. Although MUC1 modulates the activity of estrogen receptor α (ER), there is no information regarding the effects of MUC1 on global gene expression patterns and the potential role of MUC1-induced genes in predicting outcome for breast cancer patients. We have developed an experimental model of MUC1-induced transformation that has identified the activation of genes involved in cholesterol and fatty acid metabolism. A 38-gene set of experimentally derived MUC1-induced genes associated with lipid metabolism was applied to the analysis of ER+ breast cancer patients treated with tamoxifen. The results obtained from 2 independent databases demonstrate that patients overexpressing MUC1 and the lipid metabolic pathways are at significantly higher risk for death and recurrence/distant metastasis. By contrast, these genes were not predictive in untreated patients. Furthermore, a positive correlation was found between expression of the 38-gene set and the ER signaling pathway. These findings indicate that (i) MUC1 regulates cholesterol and fatty acid metabolism, and (ii) activation of these pathways in ER~+ breast cancers predicts failure to tamoxifen treatment.rnbreast cancer; expression profiling; lipid metabolism cholesterol biosynthesis; risk factors
机译:黏蛋白1(MUC1)癌蛋白在人类乳腺癌中异常过表达。尽管MUC1调节雌激素受体α(ER)的活性,但没有关于MUC1对整体基因表达模式的影响以及MUC1诱导的基因在预测乳腺癌患者预后方面的潜在作用的信息。我们已经开发了一种MUC1诱导转化的实验模型,该模型已经确定了参与胆固醇和脂肪酸代谢的基因的激活。将38个基因组的实验性MUC1诱导的基因与脂质代谢相关联,用于分析他莫昔芬治疗的ER +乳腺癌患者。从2个独立的数据库获得的结果表明,过表达MUC1的患者和脂质代谢途径的死亡和复发/远处转移的风险明显更高。相比之下,这些基因在未经治疗的患者中不能预测。此外,发现38基因集的表达与ER信号通路之间存在正相关。这些发现表明(i)MUC1调节胆固醇和脂肪酸代谢,(ii)ER〜+乳腺癌中这些途径的激活预示他莫昔芬治疗失败。表达分析脂质代谢胆固醇的生物合成;风险因素

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