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内皮素 B 受体促进恶性脑胶质瘤的增殖和免疫逃避。

Endothelin B receptor promotes the proliferation and immune escape of malignant gliomas.

机构信息

a Department of Neurosurgery , The General Hospital of Shenyang Military , Shenyang , Liaoning , China.

出版信息

Artif Cells Nanomed Biotechnol. 2018 Sep;46(6):1230-1235. doi: 10.1080/21691401.2017.1366336. Epub 2017 Aug 25.

Abstract

PURPOSE

As a kind of difficult to cure tumour, malignant gliomas have attracted widespread attention. The proliferation and immune escape of tumour cells were closely related to the development of malignant gliomas. The aim of this study was to investigate the role of endothelin B receptor (NTBR) in gliomas.

METHODS

RT-PCR was used to detect the expression of NTBR mRNA in glioma tissue and glioma cell lines. The expression of NTBR in glioma tissues was detected by immunohistochemistry. MTT assay was used to detect the viability of U87 cells after adding NTBR. Cell cloning assay was used to detect the cell proliferation ability. Western blot was used to detect the expression of TGF-β and the expression of Treg after adding NTBR to U87.

RESULT

The expression of NTBR in glioma tissues and cells was significantly higher than that in the control group by RT-PCR. After adding NTBR, cell proliferation of U87 was significantly enhanced and TGF-β and Treg were significantly expressed. It was suggested that NTBR could contribute to tumour immune escape in glioma, and it was found that there was a positive correlation between NTBR expression and different stages in malignant gliomas.

CONCLUSION

Endothelin B receptor can increase the proliferation of glioma cells and tumour immune escape. The expression of endothelin B is closely related to the clinical stage of glioma.

摘要

目的

恶性脑胶质瘤是一种难以治愈的肿瘤,引起了广泛关注。肿瘤细胞的增殖和免疫逃逸与恶性脑胶质瘤的发展密切相关。本研究旨在探讨内皮素 B 受体(NTBR)在脑胶质瘤中的作用。

方法

采用 RT-PCR 检测脑胶质瘤组织和脑胶质瘤细胞系中 NTBR mRNA 的表达,免疫组织化学检测脑胶质瘤组织中 NTBR 的表达。用 MTT 法检测加入 NTBR 后 U87 细胞的活力,用细胞克隆实验检测细胞增殖能力,用 Western blot 检测加入 NTBR 后 U87 中 TGF-β和 Treg 的表达。

结果

RT-PCR 结果显示,脑胶质瘤组织和细胞中 NTBR 的表达明显高于对照组。加入 NTBR 后,U87 细胞的增殖明显增强,TGF-β和 Treg 的表达明显增加。提示 NTBR 可促进脑胶质瘤的肿瘤免疫逃逸,且 NTBR 的表达与恶性脑胶质瘤的不同分期呈正相关。

结论

内皮素 B 受体可促进脑胶质瘤细胞的增殖和肿瘤免疫逃逸。内皮素 B 的表达与脑胶质瘤的临床分期密切相关。

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