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NME4 modulates PD-L1 expression via the STAT3 signaling pathway in squamous cell carcinoma

机译:NME4通过鳞状细胞癌中的STAT3信号通路调节PD-L1表达

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摘要

NME4, also named Nm23-H4, is a contraction of NME/NM23 Nucleoside Diphosphate Kinase 4, whose major role is the synthesis of nucleoside triphosphates. However, its association with programmed death ligand 1 (PD-L1) remains far from understood. Herein, it was discovered that silencing NME4 can lead to the marked downregulation of PD-L1, with phosphorylated STAT3 at the 705th serine being inactivated in vitro in esophageal squamous cell carcinoma (ESCC) cell lines. To further validate the association between NME4 and PD-L1 that was observed in cell lines, Pearson correlation analysis was performed on the data regarding the transcriptomic RNA sequencing of NME4 and PD-L1 in cervical squamous cell carcinoma (CSCC), which pathologically highly resembles ESCC in terms of tumor origin, obtained from the GEPIA database. It was demonstrated that their correlation was significant but negative between NME4 and PD-L1 in CSCC. To the best of our knowledge, this is the first report describing a modulation exerted by NME4 over PD-L1 in the background of squamous cell carcinoma, strongly suggestive of the underlying role of NME4 working to exclude CD8 T cells from infiltrating into the squamous cell carcinoma microenvironment. (C) 2020 Elsevier Inc. All rights reserved.
机译:NME4也命名为NM23-H4,是NME / NM23核苷二磷酸激酶4的收缩,其主要作用是合成核苷三磷酸酯。然而,它与编程死亡配体1(PD-L1)的关系仍然远未理解。在此,发现沉默的NME4可以导致PD-L1的标记下调,其中在第705次丝氨酸中具有磷酸化的STAT3在食道鳞状细胞癌(ESCC)细胞系中的体外灭活。为了进一步验证在细胞系中观察到的NME4和PD-L1之间的关联,对宫颈鳞状细胞癌(CSCC)中NME4和PD-L1的转录组RNA测序的数据进行Pearson相关分析,其病于病理学高度ESCC在肿瘤起源方面,从Gepia数据库获得。结果表明,其相关性在CSCC中的NME4和PD-L1之间具有显着性而是阴性。据我们所知,这是描述在鳞状细胞癌的背景中NME4在PD-L1上施加的调节的第一份报告,强烈暗示NME4工作以将CD8 T细胞排除到鳞状细胞中的潜在作用癌细胞。 (c)2020 Elsevier Inc.保留所有权利。

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