Li Ren, Wang Yuan-Yuan, Wang Shu-Le, Li Xue-Peng, Chen Yang, Li Zi-Ao, He Jian-Hang, Zhou Zi-Han, Li Jia-Yu, Guo Xiao-Long, Wang Xiao-Gang, Wu Yong-Qiang, Ren Ye-Qing, Zhang Wen-Ju, Wang Xiao-Man, Guo Geng
Department of Neurosurgery, The First Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Department of Radiology, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Front Genet. 2022 Sep 16;13:956632. doi: 10.3389/fgene.2022.956632. eCollection 2022.
Guanylate binding protein 2 (GBP2) is a member of the guanine binding protein family, and its relationship with prognostic outcomes and tumor immune microenvironments in glioma remains elusive. We found GBP2 were increased in glioma tissues at both mRNA and protein levels. Kaplan-Meier curves revealed that high GBP2 expression was linked with worse survival of glioma patients, and multivariate Cox regression analysis indicated that high GBP2 expression was an independent prognostic factor for glioma. Combined analysis in immune database revealed that the expression of GBP2 was significantly related to the level of immune infiltration and immunomodulators. Single-cell analysis illustrated the high expression of GBP2 in malignant glioma cells showed the high antigen presentation capability, which were confirmed by real-time polymerase chain reaction (qRT-PCR) data. Additionally, the hsa-mir-26b-5p and hsa-mir-335-5p were predicted as GBP2 regulators and were validated in U87 and U251 cells. Our results first decipher immune-related characteristics and noncoding regulators of GBP2 in glioma, which may provide insights into associated immunotherapies and prognostic predictor.
鸟苷酸结合蛋白2(GBP2)是鸟嘌呤结合蛋白家族的成员,其与胶质瘤的预后结果和肿瘤免疫微环境之间的关系仍不清楚。我们发现GBP2在胶质瘤组织中的mRNA和蛋白质水平均升高。Kaplan-Meier曲线显示,GBP2高表达与胶质瘤患者较差的生存率相关,多变量Cox回归分析表明,GBP2高表达是胶质瘤的独立预后因素。免疫数据库中的联合分析显示,GBP2的表达与免疫浸润水平和免疫调节剂显著相关。单细胞分析表明,恶性胶质瘤细胞中GBP2的高表达显示出高抗原呈递能力,这一结果得到了实时聚合酶链反应(qRT-PCR)数据的证实。此外,hsa-mir-26b-5p和hsa-mir-335-5p被预测为GBP2的调节因子,并在U87和U251细胞中得到验证。我们的结果首次揭示了胶质瘤中GBP2的免疫相关特征和非编码调节因子,这可能为相关免疫治疗和预后预测提供见解。