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RNA干扰介导的辐射诱导的基质金属蛋白酶-9下调通过激活IOMM-Lee细胞中的细胞外信号调节激酶(ERK)和蛋白激酶B(Akt)导致细胞凋亡。

RNAi-mediated downregulation of radiation-induced MMP-9 leads to apoptosis via activation of ERK and Akt in IOMM-Lee cells.

作者信息

Gogineni Venkateswara Rao, Kargiotis Odysseas, Klopfenstein Jeffrey D, Gujrati Meena, Dinh Dzung H, Rao Jasti S

机构信息

Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, Peoria, IL 61605, USA.

出版信息

Int J Oncol. 2009 Jan;34(1):209-18.

Abstract

Patients afflicted with meningiomas are most often treated with radiation therapy followed by surgical resection. However, resistance to radiation treatment has been well documented among different cancers of the brain. In this study, we demonstrate that the malignant meningioma cells (IOMM-Lee cells) overexpress MMP-9 at both the mRNA and protein levels after radiation treatment. We confirmed an increase in the invasive potential of irradiated cells through spheroid migration and matrigel invasion assays. Knockdown of MMP-9 using an adenoviral siRNA construct blocked MMP-9 expression, reduced the invasive nature of cells, and subsequently led to apoptosis. Western blot analysis revealed the activation of ERK, Akt and Fas as well as a decrease in c-JUN levels. Cleavage of PARP and TUNEL-positive characteristics confirmed apoptotic cell death in Ad-MMP-9 infected cells. Treatment with U0126 and transfection with dominant negative ERK plasmid resulted in the decreased phosphorylation of ERK and Akt. Ectopic expression of HA myr-Akt was found to be associated with an increase in pERK, and treatment with LY294002 was shown to block the phosphorylation of Akt and ERK with the restoration of c-JUN. In conclusion, our data suggest that radiation increases MMP-9 expression and the invasive nature of IOMM-Lee cells, both of which can be reversed with siRNA-mediated downregulation of MMP-9, which leads to ERK and Akt-mediated apoptosis.

摘要

患有脑膜瘤的患者最常接受放射治疗,随后进行手术切除。然而,脑部不同癌症对放射治疗的抗性已有充分记录。在本研究中,我们证明恶性脑膜瘤细胞(IOMM-Lee细胞)在放射治疗后,在mRNA和蛋白质水平上均过度表达MMP-9。我们通过球体迁移和基质胶侵袭试验证实了受辐射细胞侵袭潜力的增加。使用腺病毒siRNA构建体敲低MMP-9可阻断MMP-9表达,降低细胞的侵袭性,并随后导致细胞凋亡。蛋白质印迹分析显示ERK、Akt和Fas的激活以及c-JUN水平的降低。PARP的切割和TUNEL阳性特征证实了Ad-MMP-9感染细胞中的凋亡细胞死亡。用U0126处理并转染显性负性ERK质粒导致ERK和Akt的磷酸化降低。发现HA myr-Akt的异位表达与pERK的增加有关,并且用LY294002处理显示可阻断Akt和ERK的磷酸化并使c-JUN恢复。总之,我们的数据表明,辐射增加了MMP-9的表达和IOMM-Lee细胞的侵袭性,而这两者均可通过siRNA介导的MMP-9下调来逆转,从而导致ERK和Akt介导的细胞凋亡。

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