极光激酶A抑制剂阿利西替尼(MLN8237)通过激活线粒体介导的途径和抑制p38丝裂原活化蛋白激酶/磷脂酰肌醇-3-激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白信号通路对人骨肉瘤U-2 OS和MG-63细胞产生促凋亡和促自噬作用。

Pro-apoptotic and pro-autophagic effects of the Aurora kinase A inhibitor alisertib (MLN8237) on human osteosarcoma U-2 OS and MG-63 cells through the activation of mitochondria-mediated pathway and inhibition of p38 MAPK/PI3K/Akt/mTOR signaling pathway.

作者信息

Niu Ning-Kui, Wang Zi-Li, Pan Shu-Ting, Ding Hui-Qiang, Au Giang H T, He Zhi-Xu, Zhou Zhi-Wei, Xiao Guozhi, Yang Yin-Xue, Zhang Xueji, Yang Tianxin, Chen Xiao-Wu, Qiu Jia-Xuan, Zhou Shu-Feng

机构信息

Department of Spinal Surgery, General Hospital of Ningxia Medical University, Yinchuan, People's Republic of China ; Department of Pharmaceutical Sciences, College of Pharmacy, University of South Florida, Tampa, FL, USA ; Department of Orthopedics, General Hospital of Tianjin Medical University, Tianjin, People's Republic of China.

Department of Spinal Surgery, General Hospital of Ningxia Medical University, Yinchuan, People's Republic of China.

出版信息

Drug Des Devel Ther. 2015 Mar 12;9:1555-84. doi: 10.2147/DDDT.S74197. eCollection 2015.

Abstract

Osteosarcoma (OS) is the most common malignant bone tumor occurring mostly in children and adolescents between 10 and 20 years of age with poor response to current therapeutics. Alisertib (ALS, MLN8237) is a selective Aurora kinase A inhibitor that displays anticancer effects on several types of cancer. However, the role of ALS in the treatment of OS remains unknown. This study aimed to investigate the effects of ALS on the cell growth, apoptosis, autophagy, and epithelial to mesenchymal transition (EMT) and the underlying mechanisms in two human OS cell lines U-2 OS and MG-63. The results showed that ALS had potent growth inhibitory, pro-apoptotic, pro-autophagic, and EMT inhibitory effects on U-2 OS and MG-63 cells. ALS remarkably induced G2/M arrest and down-regulated the expression levels of cyclin-dependent kinases 1 and 2 and cyclin B1 in both U-2 OS and MG-63 cells. ALS markedly induced mitochondria-mediated apoptosis with a significant increase in the expression of key pro-apoptotic proteins and a decrease in main anti-apoptotic proteins. Furthermore, ALS promoted autophagic cell death via the inhibition of phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) and p38 mitogen-activated protein kinase (p38 MAPK) signaling pathways, and activation of 5'-AMP-dependent kinase (AMPK) signaling pathway. Inducers or inhibitors of apoptosis or autophagy simultaneously altered ALS-induced apoptotic and autophagic death in both U-2 OS and MG-63 cells, suggesting a crosstalk between these two primary modes of programmed cell death. Moreover, ALS suppressed EMT-like phenotypes with a marked increase in the expression of E-cadherin but a decrease in N-cadherin in U-2 OS and MG-63 cells. ALS treatment also induced reactive oxygen species (ROS) generation but inhibited the expression levels of sirtuin 1 and nuclear factor-erythroid-2-related factor 2 (Nrf2) in both cell lines. Taken together, these findings show that ALS promotes apoptosis and autophagy but inhibits EMT via PI3K/Akt/mTOR, p38 MAPK, and AMPK signaling pathways with involvement of ROS- and sirtuin 1-associated pathways in U-2 OS and MG-63 cells. ALS is a promising anticancer agent in OS treatment and further studies are needed to confirm its efficacy and safety in OS chemotherapy.

摘要

骨肉瘤(OS)是最常见的恶性骨肿瘤,主要发生在10至20岁的儿童和青少年中,对当前治疗方法反应不佳。阿利西替尼(ALS,MLN8237)是一种选择性极光激酶A抑制剂,对多种癌症具有抗癌作用。然而,ALS在OS治疗中的作用尚不清楚。本研究旨在探讨ALS对两种人OS细胞系U-2 OS和MG-63的细胞生长、凋亡、自噬和上皮-间质转化(EMT)的影响及其潜在机制。结果表明,ALS对U-2 OS和MG-63细胞具有强大的生长抑制、促凋亡、促自噬和EMT抑制作用。ALS显著诱导G2/M期阻滞,并下调U-2 OS和MG-63细胞中细胞周期蛋白依赖性激酶1和2以及细胞周期蛋白B1的表达水平。ALS显著诱导线粒体介导的凋亡,关键促凋亡蛋白的表达显著增加,主要抗凋亡蛋白的表达减少。此外,ALS通过抑制磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(Akt)/雷帕霉素哺乳动物靶点(mTOR)和p38丝裂原活化蛋白激酶(p38 MAPK)信号通路以及激活5'-AMP依赖性激酶(AMPK)信号通路促进自噬性细胞死亡。凋亡或自噬的诱导剂或抑制剂同时改变了ALS诱导的U-2 OS和MG-63细胞的凋亡和自噬性死亡,表明这两种程序性细胞死亡的主要模式之间存在相互作用。此外,ALS抑制了U-2 OS和MG-63细胞中类似EMT的表型,E-钙黏蛋白的表达显著增加,而N-钙黏蛋白的表达减少。ALS处理还诱导了活性氧(ROS)的产生,但抑制了两种细胞系中沉默调节蛋白1和核因子红系2相关因子2(Nrf2)的表达水平。综上所述,这些发现表明,ALS通过PI3K/Akt/mTOR、p38 MAPK和AMPK信号通路促进凋亡和自噬,但抑制EMT,在U-2 OS和MG-63细胞中涉及ROS和沉默调节蛋白1相关通路。ALS是一种有前途的OS治疗抗癌药物,需要进一步研究以证实其在OS化疗中的疗效和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f3f/4362906/fe2c641ab469/dddt-9-1555Fig1.jpg

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