IL-33在头颈鳞状细胞癌中的表达及与预后的相关性

林瀚青, 文译辉, 文卫平. IL-33在头颈鳞状细胞癌中的表达及与预后的相关性[J]. 临床耳鼻咽喉头颈外科杂志, 2018, 32(12): 895-898. doi: 10.13201/j.issn.1001-1781.2018.12.004
引用本文: 林瀚青, 文译辉, 文卫平. IL-33在头颈鳞状细胞癌中的表达及与预后的相关性[J]. 临床耳鼻咽喉头颈外科杂志, 2018, 32(12): 895-898. doi: 10.13201/j.issn.1001-1781.2018.12.004
LIN Hanqing, WEN Yihui, WEN Weiping. Correlation between prognosis and IL-33 expression in head and neck squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2018, 32(12): 895-898. doi: 10.13201/j.issn.1001-1781.2018.12.004
Citation: LIN Hanqing, WEN Yihui, WEN Weiping. Correlation between prognosis and IL-33 expression in head and neck squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2018, 32(12): 895-898. doi: 10.13201/j.issn.1001-1781.2018.12.004

IL-33在头颈鳞状细胞癌中的表达及与预后的相关性

  • 基金项目:

    广东省自然基金(No:2015A030310236,No:2017A030310362)

详细信息
    通讯作者: 文卫平,E-mail:wenwp@mail.sysu.edu.cn
  • 中图分类号: R739.91

Correlation between prognosis and IL-33 expression in head and neck squamous cell carcinoma

More Information
  • 目的:探讨头颈部鳞状细胞癌(HNSCC)患者组织中IL-33的表达情况与肿瘤临床病理特征及患者预后的相关性。方法:手术获取20例HNSCC患者肿瘤组织及对应癌旁正常组织,应用实时荧光定量PCR、免疫组织化学检测IL-33在不同组织中的表达;选取就诊于中山大学附属第一医院的107例HNSCC患者进行随访,通过免疫组织化学评估肿瘤组织IL-33的表达与肿瘤临床病理特征及预后的关系。结果:正常组织中IL-33主要表达于上皮细胞,正常组织IL-33 mRNA以及蛋白表达明显高于肿瘤组织;T3~4期及晚期(Ⅲ~Ⅳ)患者肿瘤组织中IL-33表达水平比T1~2期及早期(Ⅰ~Ⅱ)低,高分化肿瘤组织中IL-33水平高于中分化及低分化组;IL-33高表达组比低表达组患者预后好。多因素分析显示IL-33水平能够作为预测HNSCC预后的独立指标。结论:IL-33与HNSCC患者肿瘤进展及预后密切相关,可作为独立预测指标,具有较大的临床价值。
  • 加载中
  • [1]

    TORRE L A, BRAY F, SIEGEL R L, et al. Global cancer statistics, 2012[J]. CA Cancer J Clin,2015,65:87-108.

    [2]

    CRUSZ S M, BALKWILL F R. Inflammation and cancer:advances and new agents[J]. Nat Rev Clin Oncol, 2015,12:584-596.

    [3]

    PREFONTAINE D, LAJOIE-KADOCH S, FOLEY S, et al. Increased expression of IL-33 in severe asthma:evidence of expression by airway smooth muscle cells[J]. J Immunol, 2009,183:5094-5103.

    [4]

    YASUDA K, MUTO T, KAWAGOE T, et al. Contribution of IL-33-activated type II innate lymphoid cells to pulmonary eosinophilia in intestinal nematode-infected mice[J]. Proc Natl Acad Sci U S A,2012,109:3451-3456.

    [5]

    LOHNING M, STROEHMANN A, COYLE A J, et al. T1/ST2 is preferentially expressed on murine Th2 cells, independent of interleukin 4, interleukin 5, and interleukin 10, and important for Th2 effector function[J]. Proc Natl Acad Sci U S A,1998,95:6930-6935.

    [6]

    WALZL G, MATTHEWS S, KENDALL S, et al. Inhibition of T1/ST2 during respiratory syncytial virus infection prevents T helper cell type 2(Th2)- but not Th1-driven immunopathology[J]. J Exp Med,2001,193:785-792.

    [7]

    CURRY J M, SPRANDIO J, COGNETTI D, et al. Tumor microenvironment in head and neck squamous cell carcinoma[J]. Semin Oncol, 2014,41:217-234.

    [8]

    SCHMITZ J, OWYANG A, OLDHAM E, et al. IL-33, an interleukin-1-like cytokine that signals via the IL-1 receptor-related protein ST2 and induces T helper type 2-associated cytokines[J]. Immunity,2005,23:479-490.

    [9]

    MOUSSION C, ORTEGA N, GIRARD J P. The IL-1-like cytokine IL-33 is constitutively expressed in the nucleus of endothelial cells and epithelial cells in vivo:a novel ‘alarmin’[J]? PLoS One,2008,3:e3331.

    [10]

    SCHIERING C, KRAUSGRUBER T, CHOMKA A, et al.The alarmin IL-33 promotes regulatory T-cell function in the intestine[J]. Nature,2014,513:564-568.

    [11]

    PASTORELLI L, GARG R R, HOANG S B, et al. Epithelial-derived IL-33 and its receptor ST2 are dysregulated in ulcerative colitis and in experimental Th1/Th2 driven enteritis[J]. Proc Natl Acad Sci U S A, 2010,107:8017-8022.

    [12]

    GAO X, WANG X, YANG Q, et al. Tumoral expression of IL-33 inhibits tumor growth and modifies the tumor microenvironment through CD8+ T and NK cells[J]. J Immunol,2015,194:438-445.

    [13]

    MATZINGER P. The danger model:a renewed sense of self[J]. Science, 2002,296:301-305.

    [14]

    CHEN C C, KOBAYASHI T, IIJIMA K, et al. IL-33 dysregulates regulatory T cells and impairs established immunologic tolerance in the lungs[J]. J Allergy Clin Immunol,2017,140:1351-1363.e7.

    [15]

    DOMINGUEZ D, YE C, GENG Z, et al. Exogenous IL-33 Restores Dendritic Cell Activation and Maturation in Established Cancer[J]. J Immunol, 2017,198:1365-1375.

  • 加载中
计量
  • 文章访问数:  90
  • PDF下载数:  46
  • 施引文献:  0
出版历程
收稿日期:  2018-04-15

目录