Ali Sikandar, Liu Shiyu, Chen Jiali, Ullah Jawad, Mou Guoyu, Huang Xiaohua
Department of Clinical Biochemistry, College of Laboratory Medicine, Dalian Medical University, Dalian, China.
Department of Breast Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Medicine (Baltimore). 2025 Jul 25;104(30):e43396. doi: 10.1097/MD.0000000000043396.
Despite significant successes, immunotherapy continues to face numerous challenges in practical applications. CD82 plays an important role in the tumor microenvironment (TME) across various cancers. However, the prognostic value of CD82 in immunotherapy and its role in the immune response remain unclear. The expression levels of CD82 in healthy human tissues were assessed using the human protein atlas (HPA) database tool. The association among CD82 expression levels, copy number variations (CNV), and methylation was explored using the gene set cancer analysis (GSCA) database. Timer tumor immune estimation resource (TIMER) database is used for immune checkpoint and immune infiltration. The LinkedOmincs database is used for enrichment analysis. The statistical inquiry was performed through the R program (version 4.4.1). The result has shown that CD82 mRNA levels were significantly downregulated in most tumor types. Abnormal CD82 mRNA expression was associated with CNV and methylation changes in tumor tissues. Furthermore, several immune checkpoint genes related to CD82 influenced prognosis and were linked to increased immune cell infiltration across various cancer forms, including liver hepatocellular carcinoma (LIHC). The prognosis of the patients under multiple cancer forms, particularly LIHC, was remarkably influenced by CD82, which plays a vital role in modulating immune infiltration. CD82 has the potential to serve as both a prognostic indicator and an immunological biomarker in human cancer. CD82 expression is frequently downregulated across various cancer associated with poor prognosis, influenced by CNV and DNA methylation alterations. Its abnormal expression correlates with changes in immune checkpoint gene activity and enhanced immune cell infiltration, notably in liver. These associations suggest that CD82 plays a significant role in shaping the tumor immune microenvironment and affects patient prognosis. Consequently, CD82 holds promise as both a prognostic biomarker and an immunomodulatory target in cancer immunotherapy.
尽管取得了显著成功,但免疫疗法在实际应用中仍面临众多挑战。CD82在各种癌症的肿瘤微环境(TME)中发挥着重要作用。然而,CD82在免疫疗法中的预后价值及其在免疫反应中的作用仍不清楚。使用人类蛋白质图谱(HPA)数据库工具评估健康人体组织中CD82的表达水平。利用基因集癌症分析(GSCA)数据库探索CD82表达水平、拷贝数变异(CNV)和甲基化之间的关联。Timer肿瘤免疫估计资源(TIMER)数据库用于免疫检查点和免疫浸润分析。LinkedOmincs数据库用于富集分析。通过R程序(版本4.4.1)进行统计查询。结果表明,大多数肿瘤类型中CD82 mRNA水平显著下调。CD82 mRNA的异常表达与肿瘤组织中的CNV和甲基化变化有关。此外,几个与CD82相关的免疫检查点基因影响预后,并与包括肝细胞癌(LIHC)在内的各种癌症类型中免疫细胞浸润增加有关。多种癌症类型患者的预后,尤其是LIHC患者的预后,受到CD82的显著影响,CD82在调节免疫浸润中起着至关重要的作用。CD82有潜力作为人类癌症的预后指标和免疫生物标志物。在各种与预后不良相关的癌症中,CD82表达经常下调,受CNV和DNA甲基化改变的影响。其异常表达与免疫检查点基因活性的变化和免疫细胞浸润增强相关,尤其是在肝脏中。这些关联表明,CD82在塑造肿瘤免疫微环境中起重要作用,并影响患者预后。因此,CD82有望作为癌症免疫疗法中的预后生物标志物和免疫调节靶点。