Hu Yuan, Liu Muyuan, Xu Shaowei, Li Shaokun, Yang Mingfeng, Su Tian, Yuan Zihong, Peng Hanwei
Department of Head and Neck Surgery, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, China (mainland).
Med Sci Monit. 2020 Nov 26;26:e927368. doi: 10.12659/MSM.927368.
BACKGROUND Dickkopf Wnt signaling pathway inhibitor (DKK) gene family, which is known to inhibit the Wnt regulation process, is widely found in cancers. However, the roles and functions of specific family members in head and neck squamous cell carcinoma (HNSCC) are still unclear. MATERIAL AND METHODS Online bioinformatics tools (Oncomine, UALCAN, Kaplan-Meier plotter, GEPIA, Metascape, and STRING) were used to analyze the relationships between distinct DKKs and HNSCC. The transcriptome expression, clinical association, functions, pathways, and protein-protein interaction networks of DKKs in HNSCC were explored. RESULTS The mRNA expression of DKK1, DKK3, and Dickkopf-like acrosomal protein 1 (DKKL1) in HNSCC was significantly higher than in normal tissues, while that of DKK4 was lower. The mRNA expression of DKK1, DKK3, and DKKL1 was elevated in higher-grade HNSCC. The mRNA expression of DKK1 and DKK3 was elevated in human papillomavirus (HPV)-negative HNSCC, while DKKL1 had a higher mRNA expression in HPV-positive HNSCC. In addition, DKK1 was significantly associated with unfavorable overall survival in HNSCC patients. DKK3 was more likely to be a negative factor for the 5-year survival rate, while DKK4 was the opposite. DKK1 function was mainly enriched in GTPase-mediated signal transduction. Porcupine O-acyltransferase, a key regulator of the Wnt signaling pathway, was also associated with DKK1 in the protein-protein interaction network. CONCLUSIONS With regard to improving the therapeutic strategies of HNSCC in the future, DKK1 could be an unfavorable prognostic biomarker. DKK3, DKK4, and DKKL1 might be potential biomarkers for HNSCC.
背景 已知Dickkopf Wnt信号通路抑制剂(DKK)基因家族可抑制Wnt调控过程,在癌症中广泛存在。然而,特定家族成员在头颈部鳞状细胞癌(HNSCC)中的作用和功能仍不清楚。材料与方法 使用在线生物信息学工具(Oncomine、UALCAN、Kaplan-Meier plotter、GEPIA、Metascape和STRING)分析不同DKK与HNSCC之间的关系。探讨了HNSCC中DKK的转录组表达、临床关联、功能、通路及蛋白质-蛋白质相互作用网络。结果 HNSCC中DKK1、DKK3和类Dickkopf顶体蛋白1(DKKL1)的mRNA表达显著高于正常组织,而DKK4的表达较低。DKK1、DKK3和DKKL1的mRNA表达在高级别HNSCC中升高。DKK1和DKK3的mRNA表达在人乳头瘤病毒(HPV)阴性的HNSCC中升高,而DKKL1在HPV阳性的HNSCC中mRNA表达较高。此外,DKK1与HNSCC患者不良的总生存期显著相关。DKK3更可能是5年生存率的负性因素,而DKK4则相反。DKK1的功能主要富集于GTPase介导的信号转导。Wnt信号通路的关键调节因子豪猪O-酰基转移酶在蛋白质-蛋白质相互作用网络中也与DKK1相关。结论 关于未来改善HNSCC的治疗策略,DKK1可能是一个不良的预后生物标志物。DKK3、DKK4和DKKL1可能是HNSCC的潜在生物标志物。