Pan Hua, Wang Xiaoqing, Huang Weiqiang, Dai Yongmei, Yang Mi, Liang Huazhen, Wu Xixi, Zhang Longshan, Huang Wenqi, Yuan Lu, Wu Yuting, Wang Yin, Liao Liwei, Huang Jihong, Guan Jian
Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Oncology, Fujian Provincial Hospital, Fuzhou, China.
Front Oncol. 2020 Oct 6;10:557157. doi: 10.3389/fonc.2020.557157. eCollection 2020.
Interferon-induced protein 44 (IFI44) containing a guanosine-5'-triphosphate (GTP) binding domain was reported to play a significant role in the immune response to autoimmune disease. However, its roles involved in cancers remain unclear. Here, we detected the expression of IFI44 in The Cancer Genome Atlas (TCGA) Pan-cancer and generally explored the effect of IFI44 on immune infiltration in the tumor microenvironment (TME). The results displayed that IFI44 was mainly located in the cytoplasm and overexpressed in head and neck squamous cell carcinoma (HNSC) samples compared with normal tissues. Survival analysis exhibited that IFI44 was remarkably associated with the clinical outcomes, particularly in lymph node-positive and locally advanced HNSC patients. Biological analysis showed that IFI44 was correlated with such immune biological processes as antigen-presenting and nuclear factor (NF)-kappa B signaling pathways. Immune signature analysis demonstrated that the expression of IFI44 was positively correlated with the infiltration of CD4 cells and macrophages as well as neutrophils in HNSC. Taken together, these data suggested that IFI44 was abnormally expressed in cancer tissues and indicated the potential impact of IFI44 on the tumor immune infiltration in HNSC.
据报道,含有鸟苷-5'-三磷酸(GTP)结合结构域的干扰素诱导蛋白44(IFI44)在自身免疫性疾病的免疫反应中发挥重要作用。然而,其在癌症中的作用仍不清楚。在此,我们检测了癌症基因组图谱(TCGA)泛癌中IFI44的表达,并全面探究了IFI44对肿瘤微环境(TME)中免疫浸润的影响。结果显示,IFI44主要位于细胞质中,与正常组织相比,在头颈部鳞状细胞癌(HNSC)样本中过表达。生存分析表明,IFI44与临床结局显著相关,尤其是在淋巴结阳性和局部晚期HNSC患者中。生物学分析表明,IFI44与抗原呈递和核因子(NF)-κB信号通路等免疫生物学过程相关。免疫特征分析表明,IFI44的表达与HNSC中CD4细胞、巨噬细胞以及中性粒细胞的浸润呈正相关。综上所述,这些数据表明IFI44在癌组织中异常表达,并提示IFI44对HNSC肿瘤免疫浸润的潜在影响。