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CXCL5在喉鳞状细胞癌微环境中积累介导的中性粒细胞浸润:肿瘤细胞逃避免疫监视的一种机制。

Neutrophil infiltration mediated by CXCL5 accumulation in the laryngeal squamous cell carcinoma microenvironment: A mechanism by which tumour cells escape immune surveillance.

作者信息

Zhang Duo, Zhou Jian, Tang Di, Zhou Lin, Chou Liang, Chou Kuang-Yen, Tao Lei, Lu Li-Ming

机构信息

Department of Otolaryngology-HNS, Eye, Ear, Nose and Throat Hospital, Shanghai Key Clinical Disciplines of Otorhinolaryngology, Fudan University School of Medicine, 83 Fenyang Road, Shanghai 200031, China; Department of Pudong Hospital, Fudan University School of Medicine, 2800 Gongwei Road, Shanghai 201300, China.

Shanghai Institute of Immunology, Shanghai Jiaotong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.

出版信息

Clin Immunol. 2017 Feb;175:34-40. doi: 10.1016/j.clim.2016.11.009. Epub 2016 Nov 19.

Abstract

The CXCL5 chemokine is important for neutrophil accumulation in tumour tissues. In this report, we attempted to clarify whether and how infiltrating tumour-associated neutrophils (TANs) in laryngeal squamous cell carcinoma (LSCC) affect the proliferation and activation of T cells. We examined chemokine expression by real-time PCR (RT-PCR) and enzyme-linked immunosorbent assay (ELISA) and performed an immunohistochemical analysis of LSCC microarrays. The relationship between CXCL5 and CD66b (a neutrophil marker) was investigated by immunofluorescence staining. We found that CXCL5 was upregulated in LSCC tissues, whereas CXCL5 levels were decreased in LSCC patient serum. Furthermore, high levels of CXCL5 were significantly correlated with intratumoural neutrophil infiltration. Compared with peripheral blood neutrophils (PBNs), TANs significantly inhibited T cell proliferation and decreased IFN-γ and TNF-α secretion. These data suggest that excessive neutrophil infiltration is associated with advanced clinical stages of LSCC (T3 or T4, III or IV, and N1 or N2).

摘要

CXCL5趋化因子对肿瘤组织中中性粒细胞的聚集很重要。在本报告中,我们试图阐明喉鳞状细胞癌(LSCC)中浸润的肿瘤相关中性粒细胞(TANs)是否以及如何影响T细胞的增殖和活化。我们通过实时聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)检测趋化因子表达,并对LSCC微阵列进行免疫组织化学分析。通过免疫荧光染色研究CXCL5与CD66b(一种中性粒细胞标志物)之间的关系。我们发现CXCL5在LSCC组织中上调,而LSCC患者血清中CXCL5水平降低。此外,高水平的CXCL5与肿瘤内中性粒细胞浸润显著相关。与外周血中性粒细胞(PBNs)相比,TANs显著抑制T细胞增殖并降低IFN-γ和TNF-α分泌。这些数据表明,中性粒细胞过度浸润与LSCC的晚期临床阶段(T3或T4、III或IV以及N1或N2)相关。

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