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神经调节蛋白2(NRG2)在胶质瘤中表达,并促进人胶质瘤细胞的迁移。

Neuregulin 2 (NRG2) is expressed in gliomas and promotes migration of human glioma cells.

作者信息

Zhao Wei-Jiang, Yi San-Jun, Ou Guan-Yong, Qiao Xin-Yu

机构信息

Cell Biology Department, Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu, China.

Center for Neuroscience, Shantou University Medical College, Shantou, Guangdong, China.

出版信息

Folia Neuropathol. 2021;59(2):189-197. doi: 10.5114/fn.2021.106460.

Abstract

INTRODUCTION

Glioma is the most common primary brain tumour in adults. Numerous studies have shown that neuregulins (NRGs) may be involved in the formation of glioma. Although NRG1 has been extensively studied in glioma, the functions of NRG2 in glioma development remain elusive.

MATERIAL AND METHODS

In the present study, we investigated the expression of NRG2 in different grades of human glioma samples, and analysed the functional effects of NRG2 in glioma cells mainly using wound healing assay and transmigration assay.

RESULTS

We found that NRG2 was differentially expressed in different grades of human glioma/glioblastoma tissues. The data from wound healing assays demonstrated that NRG2 can differentially promote the migration of SHG44 human glioma, and U251 and U-87 MG human glioblastoma cells at different time points. The results of cell transmigration assays showed that, compared with the vehicle control, the number of cells that migrated to the underside of the insert was increased significantly for all the 3 cell lines treated with 5 nM of NRG2 for 12 hours.

CONCLUSIONS

In conclusion, our results demonstrated that NRG2 is expressed in gliomas to varying extents, and it may play roles in the migration of glioma cells in vitro. These data suggest that treatment targeting NRG2 signalling may partly reverse the migration-based metastasis of glioma cells.

摘要

引言

胶质瘤是成人中最常见的原发性脑肿瘤。众多研究表明,神经调节蛋白(NRGs)可能参与胶质瘤的形成。尽管NRG1已在胶质瘤中得到广泛研究,但NRG2在胶质瘤发展中的功能仍不清楚。

材料与方法

在本研究中,我们调查了NRG2在不同分级的人类胶质瘤样本中的表达,并主要使用伤口愈合试验和迁移试验分析了NRG2在胶质瘤细胞中的功能作用。

结果

我们发现NRG2在不同分级的人类胶质瘤/胶质母细胞瘤组织中差异表达。伤口愈合试验的数据表明,NRG2在不同时间点可差异促进SHG44人类胶质瘤细胞以及U251和U - 87 MG人类胶质母细胞瘤细胞的迁移。细胞迁移试验结果显示,与载体对照相比,用5 nM的NRG2处理12小时的所有3种细胞系迁移到小室下侧的细胞数量均显著增加。

结论

总之,我们的结果表明NRG2在胶质瘤中不同程度表达,并且它可能在体外胶质瘤细胞迁移中发挥作用。这些数据表明,靶向NRG2信号通路的治疗可能部分逆转基于迁移的胶质瘤细胞转移。

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