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Influence of Epstein–Barr virus and human papillomavirus infection on macrophage migration inhibitory factor and macrophage polarization in nasopharyngeal carcinoma

机译:对斯坦伊氏菌病毒和人乳头瘤病毒感染对巨噬细胞迁移抑制因子和巨噬细胞极化在鼻咽癌中的影响

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To assess the effects of Epstein–Barr virus (EBV) and human papillomavirus (HPV) infection on the tumor microenvironment, we examined the relationship between viral infection status, macrophage migration inhibitory factor (MIF), and tumor-associated macrophages in nasopharyngeal carcinoma (NPC). A tissue microarray containing 150 cores from 90 patients with NPC and six with chronic inflammation was used. EBV and HPV status were detected using in situ hybridization with commercial EBER1 and HPV16/18 probes. Immunofluorescence double staining of MIF, pan-macrophage marker CD68, M1 macrophage marker CD11c, and M2 macrophage marker CD163 were analyzed using the same tissue microarray. The levels of these markers between NPC and inflammation cases and between tumor nests and stroma were compared. Correlations among these markers were analyzed. We found EBER1( ) cases in 90% of NPC patients, including 10% EBV/HPV co-infection. M1 macrophages mainly infiltrated the tumor nest, while M2 macrophages infiltrated the tumor stroma. We found a significant positive correlation between EBER1 levels and MIF levels in tumor nests and a significant positive correlation between HPV16/18 and CD11c( ) cell levels in NPC tissues. It is suggested that MIF is associated with EBV, and M1 macrophage infiltration is affected by HPV status in NPC.
机译:为了评估Epstein-Barr病毒(EBV)和人乳头瘤病毒(HPV)感染对肿瘤微环境的影响,我们检查了病毒感染状态,巨噬细胞迁移抑制因子(MIF)之间的关系,鼻咽癌肿瘤相关巨噬细胞( NPC)。使用含有来自90例NPC患者和六种具有慢性炎症的患者的组织微阵列。使用商业EBER1和HPV16 / 18探头以原位杂交检测EBV和HPV状态。使用相同的组织微阵列分析MIF,PAN-巨噬细胞标记CD68,M1巨噬细胞标记CD11C和M2巨噬细胞标记CD163的免疫荧光双染色。比较了NPC和炎症病例与肿瘤巢和基质之间的这些标志物的水平。分析了这些标志物之间的相关性。我们发现90%的NPC患者的EBER1()病例,包括10%EBV / HPV共感染。 M1巨噬细胞主要渗透肿瘤巢,而M2巨噬细胞渗透肿瘤基质。我们发现肿瘤巢中Eber1水平和MIF水平与NPC组织中HPV16 / 18和CD11C()细胞水平的显着正相关性的显着正相关性。建议MIF与EBV相关,M1巨噬细胞渗透受NPC中HPV状态的影响。

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