Li Zhi, Yang Wuping, Qiu Jianhui, Xu Haozhe, Fan Bo, Li Ke, Zhou Jingcheng, Li Yuan
Department of Urology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Department of Urology, Peking University First Hospital, Beijing 100034, P.R. China.
J Cancer. 2021 Sep 13;12(22):6640-6655. doi: 10.7150/jca.62394. eCollection 2021.
Emerging evidences have indicated that IRF6, as a member of the Interferon regulatory factors (IRFs) family, plays important roles in a variety of tumors. However, the expression status of IRF6 and its prognostic value in clear cell renal cell carcinoma (ccRCC) remain unclear. In this study, we used TCGA-KIRC, GEO and TIP databases and immunohistochemistry staining to determine the expression profile, clinico-pathological features and prognostic value of IRF6 in ccRCC. MSP and demethylation analysis were utilized to verify the regulatory effect of DNA methylation on IRF6 expression. Our results found that IRF6 expression was downregulated in ccRCC tissues and cell lines, and decreased IRF6 expression was associated with worse clinicopathological features and poorer prognosis. Besides, the results of multivariate Cox regression analysis also confirmed that decreased IRF6 expression was an independently risk factor predictor of shorter Overall Survival (OS) (HR: 0.8524, 95%CI: 0.7614-0.9543, P=0.0056) and Disease Free Survival (DFS) (HR: 0.7024, 95%CI: 0.6087-0.8104, P<0.0001) in ccRCC patients. Moreover, the results of MSP and demethylation analysis validated that decreased IRF6 expression was caused by DNA hypermethylation. Furthermore, our results showed that IRF6 expression was associated with the infiltration levels of multiple immune cells in ccRCC. These findings demonstrated that IRF6 expression was significantly reduced in ccRCC and DNA hypermethylation played an important role in decreased IRF6 expression. In addition, the decrease of IRF6 was related to the unfavorable prognosis of ccRCC patients and the alterations of tumor immune cells infiltration.
新出现的证据表明,作为干扰素调节因子(IRFs)家族的一员,IRF6在多种肿瘤中发挥重要作用。然而,IRF6在肾透明细胞癌(ccRCC)中的表达状态及其预后价值仍不清楚。在本研究中,我们使用TCGA-KIRC、GEO和TIP数据库以及免疫组织化学染色来确定IRF6在ccRCC中的表达谱、临床病理特征和预后价值。利用甲基化特异性PCR(MSP)和去甲基化分析来验证DNA甲基化对IRF6表达的调节作用。我们的结果发现,IRF6在ccRCC组织和细胞系中表达下调,IRF6表达降低与更差的临床病理特征和更差的预后相关。此外,多因素Cox回归分析结果也证实,IRF6表达降低是ccRCC患者总生存期(OS)缩短(HR:0.8524,95%CI:0.7614-0.9543,P=0.0056)和无病生存期(DFS)缩短(HR:0.7024,95%CI:0.6087-0.8104,P<0.0001)的独立危险因素预测指标。此外,MSP和去甲基化分析结果证实,IRF6表达降低是由DNA高甲基化引起的。此外,我们的结果表明,IRF6表达与ccRCC中多种免疫细胞的浸润水平相关。这些发现表明,IRF6在ccRCC中表达显著降低,DNA高甲基化在IRF6表达降低中起重要作用。此外,IRF6的降低与ccRCC患者的不良预后以及肿瘤免疫细胞浸润的改变有关。