Suppr超能文献

通过针对乳腺癌细胞克隆中的 PI3K/AKT/mTOR 通路克服来曲唑获得性耐药。

Overcoming acquired resistance to letrozole by targeting the PI3K/AKT/mTOR pathway in breast cancer cell clones.

机构信息

Department of Experimental Medicine, Unit of Experimental Oncology, University of Parma, Italy.

Department of Experimental Medicine, Unit of Experimental Oncology, University of Parma, Italy.

出版信息

Cancer Lett. 2012 Oct 1;323(1):77-87. doi: 10.1016/j.canlet.2012.03.034. Epub 2012 Apr 3.

Abstract

Development of resistance to endocrine therapy is a clinical issue in estrogen receptor (ER)-positive breast cancer. Here we show that persistent activation of AKT/mTOR signaling is crucial to the acquisition of letrozole resistance in cell clones generated from MCF-7/AROM-1 aromatase-expressing breast cancer cells after prolonged letrozole exposure. ERα plays a marginal role in this context. As a proof of concept, the association between PI3K/AKT/mTOR signaling and insensitivity to endocrine therapies was confirmed in breast cancer patients who developed early letrozole resistance in neoadjuvant setting. In addition our results suggest that, regardless of the mechanism mediating the activation of AKT/mTOR pathway, either RAD001 or NVP-BEZ235 treatment may represent a promising strategy to overcome acquired resistance to letrozole in breast cancers dependent on AKT/mTOR signaling.

摘要

内分泌治疗耐药的发展是雌激素受体(ER)阳性乳腺癌的一个临床问题。在这里,我们表明,在持续的来曲唑暴露后,从 MCF-7/AROM-1 芳香酶表达乳腺癌细胞中产生的细胞克隆中,AKT/mTOR 信号的持续激活对于获得来曲唑耐药至关重要。在这种情况下,ERα 作用不大。作为概念验证,在新辅助治疗中早期来曲唑耐药的乳腺癌患者中,证实了 PI3K/AKT/mTOR 信号与对内分泌治疗不敏感之间的关联。此外,我们的结果表明,无论介导 AKT/mTOR 通路激活的机制如何,RAD001 或 NVP-BEZ235 治疗都可能是克服依赖 AKT/mTOR 信号的乳腺癌对来曲唑获得性耐药的一种有前途的策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验