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AMPK 和 p62/SQSTM1 依赖性自噬介导致逆醇诱导的慢性髓性白血病细胞死亡。

AMPK- and p62/SQSTM1-dependent autophagy mediate resveratrol-induced cell death in chronic myelogenous leukemia.

机构信息

Inserm U895, Nice, France.

出版信息

Autophagy. 2010 Jul;6(5):655-7. doi: 10.4161/auto.6.5.12126. Epub 2010 Jul 1.

DOI:10.4161/auto.6.5.12126
PMID:20458181
Abstract

Resveratrol (RSV) is an attractive candidate for cancer therapy via its ability to intervene at different levels in the AMPK/mTOR pathway. Indeed, RSV is unique in its capacity to inhibit both mTOR and S6 kinase and to activate AMPK. Our recent data reveals that RSV triggered autophagic cell death (ACD) in Chronic Myelogenous Leukemia (CML) cells, via both AMPK activation and JNK-mediated p62/SQSTM1 expression. Here we discuss how Resveratrol can mediate ACD in CML cells and the possibility of utilizing the AMPK/mTOR and JNK/p62 pathways via Resveratrol to combat CML and other hematopoietic malignancies.

摘要

白藜芦醇(RSV)通过其在 AMPK/mTOR 通路的不同水平发挥作用的能力,成为癌症治疗的一个有吸引力的候选药物。事实上,RSV 具有抑制 mTOR 和 S6 激酶并激活 AMPK 的独特能力。我们最近的数据显示,RSV 通过 AMPK 激活和 JNK 介导的 p62/SQSTM1 表达,在慢性髓性白血病(CML)细胞中引发自噬性细胞死亡(ACD)。在这里,我们讨论白藜芦醇如何在 CML 细胞中介导 ACD,以及通过白藜芦醇利用 AMPK/mTOR 和 JNK/p62 途径来对抗 CML 和其他血液恶性肿瘤的可能性。

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AMPK- and p62/SQSTM1-dependent autophagy mediate resveratrol-induced cell death in chronic myelogenous leukemia.AMPK 和 p62/SQSTM1 依赖性自噬介导致逆醇诱导的慢性髓性白血病细胞死亡。
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