[MIF in head and neck cancer: a new therapeutic target ?].

J R Lechien, N Kindt, P de Araujo Costa, G Chantrain, J Preillon, G Laurent, S Saussez
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Abstract

Macrophage migration inhibitory factor is a critical proinflammatory cytokine produced by cells of innate and adaptive immune system. MIF plays a key role in cell cycle regulation and in the pathogenesis of many cancers. Recently, MIF has been studied in the upper aerodigestive tract cancer for its involvement in tumor progression, invasion, proliferation and cell motility. In addition, MIF appears to be a mediator in angiogenesis and in the development of metastasis and locoregional lymph node, which are often associated with a poor prognosis. The mechanisms of action responsible for MIF involvement in tumor progression are not completely elucidated. However, the main effects of MIF are mediated by the CD74 receptor. MIF binding to its receptor is responsible for the activation of several signaling pathways (ERK1/2 - MAPK, JAB1 - CSN5, PI3K - Akt), the inhibition of p53 and the stimulation of angiogenic factors including VEGF and IL-8. The overexpression of MIF also causes a reduction of the anti-tumor activity of the immune system. Finally, MIF could be an interesting biomarker in the diagnosis and monitoring of upper aerodigestive tract cancers. In this paper, we assess the state of knowledge of MIF involvement in upper aero-digestive tract cancers and we analyze the therapeutic perspectives.

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[头颈癌的MIF:一个新的治疗靶点?]
巨噬细胞迁移抑制因子是先天免疫和适应性免疫细胞产生的重要促炎细胞因子。MIF在细胞周期调控和许多癌症的发病机制中起着关键作用。最近,MIF在上消化道肿瘤中参与肿瘤进展、侵袭、增殖和细胞运动被研究。此外,MIF似乎是血管生成、转移和局部区域淋巴结发展的中介,这通常与预后不良有关。MIF参与肿瘤进展的作用机制尚未完全阐明。然而,MIF的主要作用是由CD74受体介导的。MIF与其受体结合负责激活几种信号通路(ERK1/2 - MAPK, JAB1 - CSN5, PI3K - Akt),抑制p53和刺激血管生成因子包括VEGF和IL-8。MIF的过度表达也会导致免疫系统抗肿瘤活性的降低。最后,MIF可能是上消化道癌症诊断和监测的一个有趣的生物标志物。在本文中,我们评估了MIF参与上气道消化道癌症的知识状态,并分析了治疗前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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