Department of Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Jiangxi Key Laboratory for Individual Cancer Therapy, Nanchang, Jiangxi, China.
Front Immunol. 2023 Feb 27;14:1058627. doi: 10.3389/fimmu.2023.1058627. eCollection 2023.
Despite great success, immunotherapy still faces many challenges in practical applications. It was previously found that family with sequence similarity 110 member A (FAM110A) participate in the regulation of the cell cycle and plays an oncogenic role in pancreatic cancer. However, the prognostic value of FAM110A in pan-cancer and its involvement in immune response remain unclear.
The Human Protein Atlas (HPA) database was used to detect the expression of FAM110A in human normal tissues, the Tumor Immune Estimation Resource (TIMER) and TIMER 2.0 databases were used to explore the association of FAM110A expression with immune checkpoint genes and immune infiltration, and the Gene Set Cancer Analysis (GSCA) database was used to explore the correlation between FAM110A expression and copy number variations (CNV) and methylation. The LinkedOmics database was used for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Statistical analysis and visualization of data from the The Cancer Genome Atlas (TCGA) or the Genotype-Tissue Expression (GTEx) databases were performed using the R software (version 3.6.3). Clinical samples were validated using immunohistochemistry.
FAM110A expression was elevated in most tumor tissues compared with that in normal tissues. CNV and methylation were associated with abnormal FAM110A mRNA expression in tumor tissues. FAM110A affected prognosis and was associated with the expression of multiple immune checkpoint genes and abundance of tumor-infiltrating immune cells across multiple types of cancer, especially in liver hepatocellular carcinoma (LIHC). FAM110A-related genes were involved in multiple immune-related processes in LIHC.
FAM110A participates in regulating the immune infiltration and affecting the prognosis of patients in multiple cancers, especially in LIHC. FAM110A may serve as a prognostic and immunological biomarker for human cancer.
尽管免疫疗法取得了巨大成功,但在实际应用中仍面临许多挑战。先前发现家族性 110 成员 A(FAM110A)参与细胞周期的调节,并在胰腺癌中发挥致癌作用。然而,FAM110A 在泛癌中的预后价值及其在免疫反应中的作用尚不清楚。
使用人类蛋白质图谱(HPA)数据库检测 FAM110A 在人正常组织中的表达,使用肿瘤免疫估计资源(TIMER)和 TIMER 2.0 数据库探讨 FAM110A 表达与免疫检查点基因和免疫浸润的关系,使用基因集癌症分析(GSCA)数据库探讨 FAM110A 表达与拷贝数变异(CNV)和甲基化的相关性。使用 LinkedOmics 数据库进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析。使用 R 软件(版本 3.6.3)对来自癌症基因组图谱(TCGA)或基因型组织表达(GTEx)数据库的数据进行统计分析和可视化。使用免疫组织化学法验证临床样本。
与正常组织相比,大多数肿瘤组织中 FAM110A 的表达升高。CNV 和甲基化与肿瘤组织中异常的 FAM110A mRNA 表达有关。FAM110A 影响预后,并与多种癌症中多种免疫检查点基因的表达和肿瘤浸润免疫细胞的丰度相关,尤其是在肝肝细胞癌(LIHC)中。FAM110A 相关基因参与了 LIHC 中的多个免疫相关过程。
FAM110A 参与调节免疫浸润,并影响多种癌症患者的预后,尤其是在 LIHC 中。FAM110A 可能作为人类癌症的预后和免疫生物标志物。