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首页> 外文期刊>Journal of Surgical Oncology >Macrophage migration inhibitory factor contributes angiogenesis by up-regulating IL-8 and correlates with poor prognosis of patients with primary nasopharyngeal carcinoma.
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Macrophage migration inhibitory factor contributes angiogenesis by up-regulating IL-8 and correlates with poor prognosis of patients with primary nasopharyngeal carcinoma.

机译:巨噬细胞迁移抑制因子通过UP-COMMETION IL-8提供血管生成,并与原发性鼻咽癌患者的预后不良相关。

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摘要

BACKGROUND AND OBJECTIVES: We aim at the association of macrophage migration inhibitory factor (MIF) with neovascularization and survival of nasopharyngeal carcinoma (NPC), and determine whether MIF is a valuable prognostic predictor for NPC patients. METHODS: One hundred and forty one cases of NPC and 25 normal tissues of nasopharynx were collected. The expression of MIF and interleukin 8 (IL-8) was evaluated in tissues microarray by immunostaining. Intratumoral microvessel density (IMD) in relation to immunostainings and clinicopathological factors were analyzed statistically as well as the follow-up data of patients. RESULTS: High-expression of both MIF (69.5%) and IL-8 (56.0%) were significantly associated with increased microvessels and lymph node metastasis. High-expression of MIF, IL-8 and higher level of IMD were correlated with either patients' overall survival or disease-specific survival in univariate analysis, but only angiogenesis and lymph node status exhibited in relation to survival of patients as independent prognostic factor of NPC by multivariate analysis. In addition, high-expression of MIF and higher level of IMD were closely associated with locoregional failure of NPC patients. CONCLUSIONS: MIF may contribute to lymph node metastasis in NPC by inducing angiogenesis through the way of upregulation of IL-8 expression in an autocrine EBV-independent pathway.
机译:背景和目标:我们的目标是在巨噬细胞迁移抑制因子(MIF)与鼻咽癌(NPC)的生存,并确定MIF是否是NPC患者的有价值的预测预测因子。方法:收集了一百四十一株NPC和鼻咽25例鼻咽癌。通过免疫染色在组织微阵列中评价MIF和白细胞介素8(IL-8)的表达。在统计上分析了与免疫抑制和临床病理因子相关的肿瘤内微血管密度(IMD)以及患者的后续数据。结果:MIF(69.5%)和IL-8(56.0%)的高表达与增加的微血线和淋巴结转移显着相关。 MIF的高表达,IL-8和较高水平的IMD与单变量分析中的患者的整体存活或疾病特异性存活相关,但只有与患者的生存表现出的血管生成和淋巴结状态作为独立预后因子NPC通过多变量分析。此外,MIF的高表达和较高水平的IMD与NPC患者的型型失败密切相关。结论:通过诱导血管生成,通过在独立的EBV的无关途径中的UL-8表达的上调方式诱导血管生成,MIF可以促进NPC中的淋巴结转移。

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