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SEPT7基因的上调抑制人胶质瘤细胞的侵袭。

Upregulation of SEPT7 gene inhibits invasion of human glioma cells.

作者信息

Xu Song, Jia Zhi-Fan, Kang Chunsheng, Huang Qiang, Wang Guangxiu, Liu Xiaozhi, Zhou Xuan, Xu Peng, Pu Peiyu

机构信息

Laboratory of Neuro-Oncology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin 300052, People's Republic of China.

出版信息

Cancer Invest. 2010 Mar;28(3):248-58. doi: 10.3109/07357900903179609.

DOI:10.3109/07357900903179609
PMID:19916744
Abstract

OBJECTIVES

To explore the role of SEPT7 in glioma cell invasion.

METHODS

SEPT7 was transfected into human glioma cell lines U251 and TJ899, the invasive abilities were evaluated by transwell assay, scratch assay, and 3-D/2-D Matrigel growth. The expression of MMP2/9, MT1-MMP, integrin alpha(v)beta(3), and TIMP1/2 was detected by immunohistochemistry, immunofluorescence, and Western blot analyses. Distribution of alpha-tubulin was examined by laser scanning confocal analysis.

RESULT

After SEPT7 trasfection, cell invasion was inhibited, expression of MMP2/9, MT1-MMP, and integrin alpha(v)beta(3) was decreased, while TIMP1/2 was increased, and alpha-tubulin was redistributed.

CONCLUSION

These results suggest that SEPT7 plays an important role in the glioma cell invasion.

摘要

目的

探讨SEPT7在胶质瘤细胞侵袭中的作用。

方法

将SEPT7转染到人胶质瘤细胞系U251和TJ899中,通过Transwell实验、划痕实验和三维/二维基质胶生长实验评估侵袭能力。采用免疫组织化学、免疫荧光和蛋白质免疫印迹分析检测基质金属蛋白酶2/9(MMP2/9)、膜型基质金属蛋白酶1(MT1-MMP)、整合素α(v)β3和金属蛋白酶组织抑制因子1/2(TIMP1/2)的表达。通过激光扫描共聚焦分析检测α-微管蛋白的分布。

结果

SEPT7转染后,细胞侵袭受到抑制,MMP2/9、MT1-MMP和整合素α(v)β3的表达降低,而TIMP1/2增加,且α-微管蛋白重新分布。

结论

这些结果表明SEPT7在胶质瘤细胞侵袭中起重要作用。

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1
Upregulation of SEPT7 gene inhibits invasion of human glioma cells.SEPT7基因的上调抑制人胶质瘤细胞的侵袭。
Cancer Invest. 2010 Mar;28(3):248-58. doi: 10.3109/07357900903179609.
2
[Study on the anti-invasion effect of SEPT7 gene for U251MG glioma cell in vitro].[SEPT7基因对U251MG胶质瘤细胞体外抗侵袭作用的研究]
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Sublethal dose of irradiation enhances invasion of malignant glioma cells through p53-MMP 2 pathway in U87MG mouse brain tumor model.亚致死剂量的辐射通过p53 - MMP 2途径增强U87MG小鼠脑肿瘤模型中恶性胶质瘤细胞的侵袭能力。
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SEPT7 overexpression inhibits glioma cell migration by targeting the actin cytoskeleton pathway.SEPT7过表达通过靶向肌动蛋白细胞骨架途径抑制胶质瘤细胞迁移。
Oncol Rep. 2016 Apr;35(4):2003-10. doi: 10.3892/or.2016.4609. Epub 2016 Feb 3.

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MiR-301a is activated by the Wnt/β-catenin pathway and promotes glioma cell invasion by suppressing SEPT7.微小RNA-301a由Wnt/β-连环蛋白信号通路激活,并通过抑制SEPT7促进胶质瘤细胞侵袭。
Neuro Oncol. 2016 Sep;18(9):1288-96. doi: 10.1093/neuonc/now044. Epub 2016 Mar 22.