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Metformin induces differentiation in acute promyelocytic leukemia by activating the MEK/ERK signaling pathway

机译:二甲双胍通过激活MEK / ERK信号通路诱导急性早幼粒细胞白血病的分化

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摘要

Recent studies have shown that metformin, a widely used antidiabetic agent, may reduce the risk of cancer development. In this study, we investigated the antitumoral effect of metformin on both acute myeloid leukemia (AML) and acute promyelocytic leukemia (APL) cells. Metformin induced apoptosis with partial differentiation in an APL cell line, NB4, but only displayed a proapoptotic effect on several non-M3 AML cell lines. Further analysis revealed that a strong synergistic effect existed between metformin and all-trans retinoic acid (ATRA) during APL cell maturation and that metformin induced the hyperphosphorylation of extracellular signal-regulated kinase (ERK) in APL cells. U0126, a specific MEK/ERK activation inhibitor, abrogated metformin-induced differentiation. Finally, we found that metformin induced the degradation of the oncoproteins PML-RARα and c-Myc and activated caspase-3. In conclusion, these results suggest that metformin treatment may contribute to the enhancement of ATRA-induced differentiation in APL, which may deepen the understanding of APL maturation and thus provide insight for new therapy strategies.
机译:最近的研究表明,广泛使用的抗糖尿病药二甲双胍可以降低癌症发展的风险。在这项研究中,我们研究了二甲双胍对急性髓细胞白血病(AML)和急性早幼粒细胞白血病(APL)细胞的抗肿瘤作用。二甲双胍诱导凋亡在APL细胞系NB4中部分分化,但仅对几种非M3 AML细胞系显示促凋亡作用。进一步的分析表明,在APL细胞成熟期间,二甲双胍和全反式维甲酸(ATRA)之间存在很强的协同作用,而二甲双胍诱导APL细胞中细胞外信号调节激酶(ERK)的过度磷酸化。 U0126,一种特定的MEK / ERK激活抑制剂,消除了二甲双胍诱导的分化。最后,我们发现二甲双胍可诱导癌蛋白PML-RARα和c-Myc降解并激活caspase-3。总之,这些结果表明二甲双胍治疗可能有助于增强ATRA诱导的APL分化,从而可能加深对APL成熟的理解,从而为新的治疗策略提供见识。

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