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神经纤毛蛋白1的表达通过预测调节性T细胞和M2巨噬细胞的浸润而作为胃腺癌的预后标志物。

Neuropilin1 Expression Acts as a Prognostic Marker in Stomach Adenocarcinoma by Predicting the Infiltration of Treg Cells and M2 Macrophages.

作者信息

Kang Ji Young, Gil Minchan, Kim Kyung Eun

机构信息

Department of Health Industry, Sookmyung Women's University, Seoul 04310, Korea.

Department of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea.

出版信息

J Clin Med. 2020 May 12;9(5):1430. doi: 10.3390/jcm9051430.

Abstract

Neuropilin1 (NRP1) plays a critical role in tumor progression and immune responses. Although the roles of NRP1 in various tumors have been investigated, the clinical relevance of NRP1 expression in stomach adenocarcinoma (STAD) has not been studied. To investigate the use of NRP1 as a prognostic biomarker of STAD, we analyzed NRP1 mRNA expression and its correlation with patient survival and immune cell infiltration using various databases. NRP1 mRNA expression was significantly higher in STAD than normal tissues, and Kaplan-Meier survival analysis showed that NRP1 expression was significantly associated with poor prognosis in patients with STAD. To elucidate the related mechanism, we analyzed the correlation between NRP1 expression and immune cell infiltration level. In particular, the infiltration of immune-suppressive cells, such as regulatory T (Treg) cells and M2 macrophage, was significantly increased by NRP1 expression. In addition, the expression of interleukin (IL)-35, IL-10, and TGF-β1 was also positively correlated with NRP1 expression, resulting in the immune suppression. Collectively in this study, our integrated analysis using various clinical databases shows that the significant correlation between NRP1 expression and the infiltration of Treg cells and M2 macrophage explains poor prognosis mechanism in STAD, suggesting the clinical relevance of NRP1 expression as a prognostic biomarker for STAD patients.

摘要

神经纤毛蛋白1(NRP1)在肿瘤进展和免疫反应中起着关键作用。尽管已经研究了NRP1在各种肿瘤中的作用,但尚未研究NRP1表达在胃腺癌(STAD)中的临床相关性。为了研究NRP1作为STAD预后生物标志物的用途,我们使用各种数据库分析了NRP1 mRNA表达及其与患者生存和免疫细胞浸润的相关性。STAD中NRP1 mRNA表达明显高于正常组织,Kaplan-Meier生存分析表明,NRP1表达与STAD患者的不良预后显著相关。为了阐明相关机制,我们分析了NRP1表达与免疫细胞浸润水平之间的相关性。特别是,NRP1表达显著增加了免疫抑制细胞的浸润,如调节性T(Treg)细胞和M2巨噬细胞。此外,白细胞介素(IL)-35、IL-10和转化生长因子-β1的表达也与NRP1表达呈正相关,从而导致免疫抑制。在本研究中,我们使用各种临床数据库进行的综合分析表明,NRP1表达与Treg细胞和M2巨噬细胞浸润之间的显著相关性解释了STAD的不良预后机制,提示NRP1表达作为STAD患者预后生物标志物的临床相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b84b/7290937/c4a044d429b1/jcm-09-01430-g001.jpg

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