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紧密连接蛋白-1/核因子κB/趋化因子配体8:肿瘤血管生成的新调控轴

Zonula occludens-1/NF-κB/CXCL8: a new regulatory axis for tumor angiogenesis.

作者信息

Lesage Julien, Suarez-Carmona Meggy, Neyrinck-Leglantier Deborah, Grelet Simon, Blacher Silvia, Hunziker Walter, Birembaut Philippe, Noël Agnes, Nawrocki-Raby Béatrice, Gilles Christine, Polette Myriam

机构信息

INSERM, Unité Mixte de Recherche-S 903, Structure Fédérative de Recherche Champagne-Ardennes Picardie-Santé (SFR CAP), University of Reims Champagne-Ardenne, Reims, France.

Laboratory of Tumor and Development Biology, Grappe Interdisciplinaire de Génoprotéomique Appliquée (GIGA)-Cancer, University of Liège, Liège, Belgium.

出版信息

FASEB J. 2017 Apr;31(4):1678-1688. doi: 10.1096/fj.201600890R. Epub 2017 Jan 5.

Abstract

Zonula occludens-1 (ZO-1) is a submembrane scaffolding protein that may display proinvasive functions when it relocates from tight junctions into the cytonuclear compartment. This article examines the functional involvement of ZO-1 in CXCL8/IL-8 chemokine expression in lung and breast tumor cells. ZO-1 small interfering RNA and cDNA transfection experiments emphasized regulation of CXCL8/IL-8 expression a cytonuclear pool of ZO-1. Luciferase reporter assays highlighted a 173-bp region of promoter that responded to ZO-1. Moreover, by using mutated promoter constructs, we identified a NF-κB site as critical in this activation. Furthermore, NF-κB pathway signaling analysis revealed both IκBα and p65 phosphorylation in ZO-1-overexpressing cells, and subsequent p65 silencing validated its requirement for CXCL8/IL-8 induction. Investigation of the functional implication of this regulatory axis next showed the proangiogenic activity of ZO-1 in both o and angiogenesis assays. Finally, we found that non-small-cell lung carcinoma that presented a cytonuclear ZO-1 pattern was significantly more angiogenic that that without detectable cytonuclear ZO-1 expression. Taken together, our results demonstrate that ZO-1 regulates CXCL8/IL-8 expression the NF-κB signaling pathway and its p65 subunit, which subsequently modulates the transcription of IL-8. We also provide evidence of a newly identified regulatory pathway that could promote angiogenesis. Thus, our results support the concept that the ZO-1 shuttle from the cell junction to the cytonuclear compartment may affect both the intrinsic invasive properties of tumor cells and the establishment of the protumoral microenvironment.-Lesage, J., Suarez-Carmona, M., Neyrinck-Leglantier, D., Grelet, S., Blacher, S., Hunziker, W., Birembaut, P., Noël, A., Nawrocki-Raby, B., Gilles, C., Polette, M. Zonula occludens-1/NF-κB/CXCL8: a new regulatory axis for tumor angiogenesis.

摘要

闭合蛋白-1(ZO-1)是一种膜下支架蛋白,当它从紧密连接重新定位到细胞核周区室时可能发挥促侵袭功能。本文研究了ZO-1在肺和乳腺肿瘤细胞中CXCL8/IL-8趋化因子表达中的功能作用。ZO-1小干扰RNA和cDNA转染实验强调了ZO-1的细胞核周池对CXCL8/IL-8表达的调控作用。荧光素酶报告基因检测突出了CXCL8/IL-8启动子的一个173bp区域对ZO-1有反应。此外,通过使用突变的启动子构建体,我们确定了一个NF-κB位点在这种激活中至关重要。此外,NF-κB信号通路分析显示在过表达ZO-1的细胞中IκBα和p65均发生磷酸化,随后p65沉默证实了其对CXCL8/IL-8诱导的必要性。接下来对这一调控轴功能意义的研究表明,ZO-1在体外和体内血管生成实验中均具有促血管生成活性。最后,我们发现呈现细胞核周ZO-1模式的非小细胞肺癌的血管生成明显高于未检测到细胞核周ZO-1表达的肿瘤。综上所述,我们的结果表明,ZO-1通过NF-κB信号通路及其p65亚基调节CXCL8/IL-8的表达,进而调节IL-8的转录。我们还提供了一条新发现的可促进血管生成的调控途径的证据。因此,我们的结果支持这样一种观点,即ZO-1从细胞连接向细胞核周区室的穿梭可能影响肿瘤细胞的内在侵袭特性以及肿瘤微环境的建立。——勒萨热,J.,苏亚雷斯-卡尔莫纳,M.,内林克-勒格兰蒂耶,D.,格雷莱特,S.,布拉歇,S.,洪齐克,W.,比伦博,P.,诺埃尔,A.,纳沃罗茨基-拉比,B.,吉尔斯,C.,波莱特,M. 闭合蛋白-1/NF-κB/CXCL8:肿瘤血管生成的新调控轴

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