Mei Zubing, Wang Guanghui, Liang Zhonglin, Cui Ang, Xu Andong, Liu Yun, Liu Chenying, Yang Yili, Cui Long
Department of Colorectal Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Colorectal Cancer Research Center, Shanghai, China.
Oncotarget. 2017 Jun 13;8(24):38969-38977. doi: 10.18632/oncotarget.17163.
Interferon regulatory factor 2 (IRF-2) is known to play a pivotal role in the development and progression of several malignancies. As a crucial member of interferon regulatory factor family, the association between the expression of IRF-2 and clinical prognostic significance has not been fully explored in colorectal cancer (CRC). The purpose of our study was to investigate the expression profile of IRF-2 in CRC and to examine its association with clinical features. The expression levels of IRF-2 in 18 paired CRC and non-cancerous colorectal tissues were measured by quantitative real-time PCR (qRT-PCR) and those in 4 paired samples by Western blotting. The results showed a significant increase in IRF-2 mRNA expression and protein expression in CRC tissues compared to those in paired normal tissues. Besides, high expression of IRF-2 was significantly associated with distant metastasis (P = 0.041) and preoperative serum CEA level (P = 0.045). Kaplan-Meier survival analysis showed that patients with high expression of IRF-2 had a significantly worse overall survival than those with low expression of IRF-2 (P = 0.006). Further multivariate analysis indicated that IRF-2 and TNM stage were independent prognostic factors for overall survival in patients with CRC. Our study primarily suggests IRF-2 as a potential prognostic biomarker in CRC.
干扰素调节因子2(IRF-2)在多种恶性肿瘤的发生和发展中起着关键作用。作为干扰素调节因子家族的重要成员,IRF-2的表达与临床预后意义之间的关联在结直肠癌(CRC)中尚未得到充分研究。我们研究的目的是调查IRF-2在CRC中的表达谱,并检查其与临床特征的关联。通过定量实时PCR(qRT-PCR)测量了18对CRC和非癌性结直肠组织中IRF-2的表达水平,并通过蛋白质印迹法测量了4对样本中的表达水平。结果显示,与配对的正常组织相比,CRC组织中IRF-2 mRNA表达和蛋白质表达显著增加。此外,IRF-2的高表达与远处转移(P = 0.041)和术前血清CEA水平(P = 0.045)显著相关。Kaplan-Meier生存分析表明,IRF-2高表达的患者总生存期明显低于IRF-2低表达的患者(P = 0.006)。进一步的多变量分析表明,IRF-2和TNM分期是CRC患者总生存期的独立预后因素。我们的研究主要表明IRF-2是CRC中一种潜在的预后生物标志物。