首页> 美国卫生研究院文献>Breast Cancer : Targets and Therapy >The ABC7 regimen: a new approach to metastatic breast cancer using seven common drugs to inhibit epithelial-to-mesenchymal transition and augment capecitabine efficacy
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The ABC7 regimen: a new approach to metastatic breast cancer using seven common drugs to inhibit epithelial-to-mesenchymal transition and augment capecitabine efficacy

机译:ABC7方案:一种转移性乳腺癌的新方法使用七种常见药物抑制上皮向间充质转化并提高卡培他滨疗效

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摘要

Breast cancer metastatic to bone has a poor prognosis despite recent advances in our understanding of the biology of both bone and breast cancer. This article presents a new approach, the ABC7 regimen (Adjuvant for Breast Cancer treatment using seven repurposed drugs), to metastatic breast cancer. ABC7 aims to defeat aspects of epithelial-to-mesenchymal transition (EMT) that lead to dissemination of breast cancer to bone. As add-on to current standard treatment with capecitabine, ABC7 uses ancillary attributes of seven already-marketed noncancer treatment drugs to stop both the natural EMT process inherent to breast cancer and the added EMT occurring as a response to current treatment modalities. Chemotherapy, radiation, and surgery provoke EMT in cancer generally and in breast cancer specifically. ABC7 uses standard doses of capecitabine as used in treating breast cancer today. In addition, ABC7 uses 1) an older psychiatric drug, quetiapine, to block RANK signaling; 2) pirfenidone, an anti-fibrosis drug to block TGF-beta signaling; 3) rifabutin, an antibiotic to block beta-catenin signaling; 4) metformin, a first-line antidiabetic drug to stimulate AMPK and inhibit mammalian target of rapamycin, (mTOR); 5) propranolol, a beta-blocker to block beta-adrenergic signaling; 6) agomelatine, a melatonergic antidepressant to stimulate M1 and M2 melatonergic receptors; and 7) ribavirin, an antiviral drug to prevent eIF4E phosphorylation. All these block the signaling pathways – RANK, TGF-beta, mTOR, beta-adrenergic receptors, and phosphorylated eIF4E – that have been shown to trigger EMT and enhance breast cancer growth and so are worthwhile targets to inhibit. Agonism at MT1 and MT2 melatonergic receptors has been shown to inhibit both breast cancer EMT and growth. This ensemble was designed to be safe and augment capecitabine efficacy. Given the expected outcome of metastatic breast cancer as it stands today, ABC7 warrants a cautious trial.
机译:尽管我们对骨骼和乳腺癌生物学的了解最近有所进展,但转移到骨骼的乳腺癌的预后很差。本文提出了一种新的方法,即ABC7方案(使用七种改用药物的乳腺癌佐剂治疗方案),用于转移性乳腺癌。 ABC7旨在克服导致乳腺癌向骨骼扩散的上皮到间充质转变(EMT)的各个方面。作为当前使用卡培他滨的标准治疗方法的补充,ABC7利用七种已经上市的非癌治疗药物的辅助属性,既可以终止乳腺癌固有的天然EMT过程,也可以停止因对当前治疗方式的反应而发生的添加EMT。化学疗法,放射疗法和手术通常会在癌症中,特别是在乳腺癌中引发EMT。 ABC7使用标准剂量的卡培他滨治疗当今的乳腺癌。此外,ABC7使用1)一种较老的精神药物喹硫平来阻断RANK信号传导; 2)吡非尼酮,一种阻断TGF-β信号传导的抗纤维化药物; 3)利福布汀,一种阻断β-catenin信号传导的抗生素; 4)二甲双胍,一线抗糖尿病药物,可刺激AMPK和抑制哺乳动物雷帕霉素靶标(mTOR); 5)普萘洛尔,一种阻断β-肾上腺素信号传导的β-受体阻滞剂; 6)阿戈美拉汀,一种褪黑素抗抑郁药,可刺激M1和M2褪黑素受体; 7)利巴韦林,一种防止eIF4E磷酸化的抗病毒药物。所有这些都阻断了RANK,TGF-β,mTOR,β-肾上腺素受体和磷酸化eIF4E的信号通路,这些信号通路已被证明可以触发EMT并增强乳腺癌的生长,因此值得抑制。 MT1和MT2褪黑素受体的激动作用已被证明可以抑制乳腺癌的EMT和生长。设计该合奏是安全的并增强卡培他滨疗效。鉴于目前转移性乳腺癌的预期结果,ABC7值得谨慎研究。

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