Abudusalam Kaderya, Xu Yan, Keyumu Pazilat, Cheng Tong, Xu Manyu, Lu Bing, Sun Pingping, Musha Kadierjiang, Huang Jianfei
Translational Medicine Center, People's Hospital of Kizilsu Kirgiz Autonomous Prefecture 845350, Xinjiang Autonomous Region, China.
Department of Clinical Biobank, Affiliated Hospital of Nantong University & Department of Pathology, Medical School of Nantong University, Nantong 226001, Jiangsu, China.
Curr Med Chem. 2024 Feb 26. doi: 10.2174/0109298673282921240220101914.
Patients with glioma have limited treatment options and experience poor prognoses. Therefore, it is urgently needed to explore new diagnostic and therapeutic targets.
This study aimed to investigate the relevance of WSC domain-containing 2 (WSCD2) expression to glioma, clinicopathological characteristics, tumor-infiltrating immune cells (TILs), and patient prognosis.
We analyzed WSCD2 mRNA expression in glioma tissues and patient survival using the Gene Expression Profiling Interactive Analysis database. Furthermore, the relationship between the expressions of WSCD2 mRNA and TILs in gliomas was evaluated utilizing the Tumor Immune Estimation Resource database. Lastly, we employed multiplex immunohistochemistry to detect the protein expressions of WSCD2 and TILs in glioma tissues.
WSCD2 mRNA expression in glioma tissues was lower than that in tissues of benign brain disease. High WSCD2 mRNA expression was also significantly associated with a favorable outcome. Additionally, WSCD2 mRNA expression was correlated with TIL expression in glioma; however, no such relationship was detected between the protein expressions of WSCD2 and TILs in glioma tissues. Cox regression multivariate analysis and Kaplan-Meier survival analysis showed that WSCD2 expression in glioma tissues could be an independent prognostic factor.
This study highlights the correlation between WSCD2 expression and TILs and demonstrates the prognostic significance of WSCD2 in glioma. Furthermore, our results suggest that WSCD2 may be a potential immunotherapy target in glioma.
胶质瘤患者的治疗选择有限,预后较差。因此,迫切需要探索新的诊断和治疗靶点。
本研究旨在探讨含WSC结构域蛋白2(WSCD2)表达与胶质瘤、临床病理特征、肿瘤浸润免疫细胞(TILs)及患者预后的相关性。
我们使用基因表达谱交互分析数据库分析胶质瘤组织中WSCD2 mRNA表达及患者生存率。此外,利用肿瘤免疫评估资源数据库评估胶质瘤中WSCD2 mRNA表达与TILs表达之间的关系。最后,我们采用多重免疫组化检测胶质瘤组织中WSCD2和TILs的蛋白表达。
胶质瘤组织中WSCD2 mRNA表达低于良性脑疾病组织。高WSCD2 mRNA表达也与良好预后显著相关。此外,WSCD2 mRNA表达与胶质瘤中的TIL表达相关;然而,在胶质瘤组织中未检测到WSCD2与TILs蛋白表达之间存在这种关系。Cox回归多因素分析和Kaplan-Meier生存分析表明,胶质瘤组织中WSCD2表达可能是一个独立的预后因素。
本研究强调了WSCD2表达与TILs之间的相关性,并证明了WSCD2在胶质瘤中的预后意义。此外,我们的结果表明WSCD2可能是胶质瘤潜在的免疫治疗靶点。