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Twist1启动子甲基化通过PI3K/AKT途径调节急性髓系白血病细胞的增殖和凋亡。

Twist1 Promoter Methylation Regulates the Proliferation and Apoptosis of Acute Myeloid Leukemia Cells via PI3K/AKT Pathway.

作者信息

Gong Aihong, Wang Xiaojia, Wang Xuewei, Zhao Ying, Cui Yanan

机构信息

Department of Medical Records Statistics Room, General Hospital of Ningxia Medical University, No. 692, Shengli South Street, Xingqing District, Yinchuan, 750004 Ningxia China.

Department of Hematology, General Hospital of Ningxia Medical University, Yinchuan, 750003 Ningxia China.

出版信息

Indian J Hematol Blood Transfus. 2023 Jan;39(1):25-32. doi: 10.1007/s12288-022-01540-2. Epub 2022 Jun 1.

Abstract

Twist-related protein 1 (Twist1) is a widely recognized oncogene in acute myeloid leukemia (AML), and its promoter methylation is related with the progression of solid tumors. However, the association between Twist1 promoter methylation and AML has not been well studied. Twist1 mRNA expression was detected using quantitative real-time polymerase chain reaction (qRT-PCR). The protein levels of Twist1 and phosphatidylinositol 3-kinase/protein kinase B (PI3K/AKT) signal were measured via western blotting. Methylation-specific PCR was performed to detect the methylation status of Twist1 promoter. CCK-8 assay and flow cytometry were used to reveal cellular biological effects. Twist1 expression and promoter methylation level were significantly upregulated in AML tissues and cell lines and were further downregulated in demethylating agent 5'-azacitidine (5-Aza)-treated cells. Ectopic expression of Twist1 increased AML cell viability, while reducing apoptosis, and attenuated the effects of 5-Aza on the proliferation and apoptosis. We also found that the PI3K/AKT signaling pathway was positively regulated by Twist1. Our findings revealed that Twist1 accelerates the tumorigenesis of AML cells by promoting its promoter methylation via the activation of PI3K/AKT signaling pathway.

摘要

Twist相关蛋白1(Twist1)是急性髓系白血病(AML)中一种广为人知的癌基因,其启动子甲基化与实体瘤的进展有关。然而,Twist1启动子甲基化与AML之间的关联尚未得到充分研究。采用定量实时聚合酶链反应(qRT-PCR)检测Twist1 mRNA表达。通过蛋白质印迹法检测Twist1和磷脂酰肌醇3激酶/蛋白激酶B(PI3K/AKT)信号的蛋白水平。进行甲基化特异性PCR检测Twist1启动子的甲基化状态。使用CCK-8法和流式细胞术揭示细胞生物学效应。Twist1表达和启动子甲基化水平在AML组织和细胞系中显著上调,在经去甲基化剂5'-氮杂胞苷(5-Aza)处理的细胞中进一步下调。Twist1的异位表达增加了AML细胞的活力,同时减少了细胞凋亡,并减弱了5-Aza对增殖和凋亡的影响。我们还发现PI3K/AKT信号通路受Twist1正向调控。我们的研究结果表明,Twist1通过激活PI3K/AKT信号通路促进其启动子甲基化,从而加速AML细胞的肿瘤发生。

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