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Combination of Rad001 (Everolimus) and propachlor synergistically induces apoptosis through enhanced autophagy in prostate cancer cells

机译:Rad001(依维莫司)与丙草胺的组合通过增强自噬作用协同诱导前列腺癌细胞凋亡

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摘要

PI3K/AKT/mTOR pathway plays a key role in the tumorigenesis ofmanyhuman cancers including prostate cancer. However, inhibitors of this pathway, such as Rad001, have not shown therapeutic efficacy as a single agent. Through a high-throughput screen of 5,000 widely used small molecules, we identified compounds that can synergize with Rad001 to inhibit prostate cancer cells. One of the compounds, propachlor, synergizes with Rad001 to induce apoptosis of castration-resistant prostate cancer cells via enhanced autophagy. This enhanced autophagic cell death is accompanied by increased Beclin1 expression as well as upregulation of Atg5-Atg12 conjugate and LC3-2. Rad001 and propachlor can also synergistically inhibit tumors in a xenograft animal model of prostate cancer. These findings provide a novel direction to develop combination therapies for advanced and metastatic prostate cancer that has failed the currently available therapies.
机译:PI3K / AKT / mTOR途径在包括前列腺癌在内的许多人类癌症的肿瘤发生中起着关键作用。但是,该途径的抑制剂,例如Rad001,尚未显示出作为单一药物的治疗功效。通过对5,000个广泛使用的小分子进行的高通量筛选,我们确定了可以与Rad001协同作用以抑制前列腺癌细胞的化合物。化合物丙草胺之一与Rad001协同作用,通过增强的自噬作用诱导去势抵抗性前列腺癌细胞的凋亡。这种自噬细胞死亡的增加伴随着Beclin1表达的增加以及Atg5-Atg12共轭物和LC3-2的上调。 Rad001和丙草胺还可以协同抑制前列腺癌异种移植动物模型中的肿瘤。这些发现为开发用于晚期和转移性前列腺癌的联合疗法提供了新的方向,而该疗法目前无法使用。

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