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小泛素样修饰特异性蛋白酶1的抑制通过调节NF-κB/Akt信号通路诱导星形胶质瘤细胞凋亡。

Inhibition of SUMO-specific protease 1 induces apoptosis of astroglioma cells by regulating NF-κB/Akt pathways.

作者信息

Xia Wenrong, Tian Hongwei, Cai Xin, Kong HaiBo, Fu Wenliang, Xing Weiwei, Wang Yuanyuan, Zou Minji, Hu Yuhua, Xu Donggang

机构信息

Laboratory of Genome Engineering, Beijing Institute of Basic Medical Sciences, Beijing 100850, China.

Department of Neurosurgery, The 2nd Hospital Affiliated to Hebei Medical University, Shijiazhuang, China.

出版信息

Gene. 2016 Dec 31;595(2):175-179. doi: 10.1016/j.gene.2016.09.040. Epub 2016 Sep 28.

Abstract

SUMO-specific protease 1 (SENP1) is an important regulation protease in the protein desumoylation, which was shown to have a prooncogenicrole in many types of cancer. However, the mechanism of action for SENP1 in astrocytoma is not yet clear. Astrocytoma is the most frequent one among various neurogliomas, of which a subtype known as glioblastoma multiforme (GBM) is the most malignant brain glioma and seriously influences the life quality of the patients. In this study, the expression of SENP1 was detected in 28 cases of various grades of astrocytoma and 6 cases of normal human tissues. The results showed that the expression of SENP1 was positively correlated with the malignant grades. Besides, the NF-κB and Akt signaling pathways in GBM tissues were activated. Cytological experiments indicated that knock-down of endogenous SENP1 promoted cell apoptosis. Further research confirmed that downexpression of SENP1 could inhibit the phosphorylation of IκBα and Akt, and also the expression of its downstream regulation factors Bcl-xL and cyclinD1. These results delineate a key role for SENP1 in astrocytoma development, suggesting it may be a potential new therapeutic target inastrocytoma.

摘要

小泛素样修饰蛋白特异性蛋白酶1(SENP1)是蛋白质去SUMO化过程中的一种重要调节蛋白酶,已证实在多种癌症中发挥促癌作用。然而,SENP1在星形细胞瘤中的作用机制尚不清楚。星形细胞瘤是各类神经胶质瘤中最常见的一种,其中一种名为多形性胶质母细胞瘤(GBM)的亚型是最恶性的脑胶质瘤,严重影响患者的生活质量。在本研究中,检测了28例不同分级的星形细胞瘤和6例正常人体组织中SENP1的表达。结果表明,SENP1的表达与恶性分级呈正相关。此外,GBM组织中的NF-κB和Akt信号通路被激活。细胞学实验表明,敲低内源性SENP1可促进细胞凋亡。进一步研究证实,SENP1的下调可抑制IκBα和Akt的磷酸化,以及其下游调节因子Bcl-xL和细胞周期蛋白D1的表达。这些结果阐明了SENP1在星形细胞瘤发展中的关键作用,表明它可能是星形细胞瘤潜在的新治疗靶点。

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