Wu Gu Jie, Ren Kuan, He Min, Xu Jian Xun, Li Zhen Qing, Bo Ding, Xue Qun
Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, People's Republic of China.
Medical College of Nantong University, Nantong, 226001, Jiangsu, People's Republic of China.
Int J Gen Med. 2021 Nov 3;14:7599-7611. doi: 10.2147/IJGM.S337198. eCollection 2021.
Sorting nexin-20 (SNX20) is a member of the sorting nexin family of proteins. It plays a crucial role in the regulation of innate immunity. However, the prognostic risk, potential mechanisms, immunotherapy, and other functions of in lung adenocarcinoma (LUAD) remain unclear.
We analyzed and validated the expression and prognostic role of in LUAD through a combination of The Cancer Genome Atlas, Gene Expression Omnibus, Oncomine, TIMER, and Human Protein Atlas databases. Further, we analyzed the correlation between expression and clinical characteristics of LUAD, and the prognostic value of in LUAD was evaluated. Using fitted expression and other clinical parameters, a predictive model with predictive performance for the overall survival of patients with LUAD was constructed. The potential biological function of in LUAD was explored using gene set enrichment analysis. In addition, we analyzed the correlation between expression and the immune microenvironment and survival.
was downregulated in most cancer types, was associated with poor prognosis in LUAD and could be an independent prognostic factor for patients with LUAD. The predictive model developed by us had good predictive power for determining the overall survival of patients with LUAD. Biofunctional analysis revealed that genes co-expressed with mainly promoted the immune process and inhibited the cell proliferation process in LUAD. We observed that high expression of was accompanied by a better immune microenvironment and survival in patients with LUAD. Furthermore, the LUAD immune response was elevated with an increase in expression. Finally, we found that expression was significantly associated with various tumor-infiltrating immune cells, and it was widely involved in regulating various immune molecules in LUAD and affecting immune infiltration in the tumor microenvironment.
Our results suggested that is a potential immune-related biomarker and therapeutic target associated with the prognosis of patients with LUAD. This provided a new strategy for the development of immunotherapeutic and prognostic markers in LUAD.
分选连接蛋白20(SNX20)是分选连接蛋白家族的成员。它在先天免疫调节中起关键作用。然而,其在肺腺癌(LUAD)中的预后风险、潜在机制、免疫治疗及其他功能仍不清楚。
我们通过整合癌症基因组图谱、基因表达综合数据库、Oncomine、TIMER和人类蛋白质图谱数据库,分析并验证了SNX20在LUAD中的表达及预后作用。此外,我们分析了SNX20表达与LUAD临床特征之间的相关性,并评估了SNX20在LUAD中的预后价值。利用拟合的SNX20表达和其他临床参数,构建了一个对LUAD患者总生存具有预测性能的预测模型。使用基因集富集分析探索了SNX20在LUAD中的潜在生物学功能。此外,我们分析了SNX20表达与免疫微环境及生存之间的相关性。
SNX20在大多数癌症类型中表达下调,与LUAD的不良预后相关,并且可能是LUAD患者的独立预后因素。我们开发的预测模型对确定LUAD患者的总生存具有良好的预测能力。生物功能分析表明,与SNX20共表达的基因主要促进LUAD中的免疫过程并抑制细胞增殖过程。我们观察到,LUAD患者中SNX20的高表达伴随着更好的免疫微环境和生存。此外,随着SNX20表达的增加,LUAD免疫反应增强。最后,我们发现SNX20表达与各种肿瘤浸润免疫细胞显著相关,并且广泛参与调节LUAD中的各种免疫分子并影响肿瘤微环境中的免疫浸润。
我们的结果表明,SNX20是一种与LUAD患者预后相关的潜在免疫相关生物标志物和治疗靶点。这为LUAD免疫治疗和预后标志物的开发提供了新策略。