IL4I1在人类肿瘤中的预后和免疫学作用的泛癌分析:大体量全息研究和单细胞测序验证

Bin Chen, Yi Liu, Yuping He, Chenfu Shen
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引用次数: 0

摘要

背景白细胞介素-4 诱导基因 1(IL4I1)调节多种肿瘤类型的肿瘤进展。然而,它与泛癌症患者的免疫浸润和预后的相关性仍不清楚。方法数据来自癌症基因组图谱(TCGA)、基因型-组织表达(GTEx)、UALCAN、临床蛋白质组肿瘤分析联盟(CPTAC)、基因表达总库(GEO)、cBioPortal、癌症单细胞状态图谱(CancerSEA)、该研究利用肿瘤 IMmune Estimation Resource (TIMER) 数据库评估 IL4I1 的表达、临床特征和预后影响、基因组富集、与免疫细胞浸润的相关性,以及 IL4I1 甲基化和表达与生存预后的关系。结果IL4I1在大多数肿瘤中显著过表达,IL4I1的失衡与总生存期和病理分期显著相关。此外,IL4I1 蛋白总量在癌症中有所增加。因此,IL4I1 可作为多种癌症的预后生物标志物或保护因素。IL4I1的甲基化水平也可作为预后标志物。IL4I1 的功能富集与免疫调节途径密切相关。scRNA-seq分析表明,IL4I1在肿瘤微环境中的不同细胞间存在显著差异,在巨噬细胞中的富集程度最高。在大多数肿瘤中,各种免疫检查点基因与IL4I1的表达呈正相关。此外,IL4I1高表达的患者可能对BMS-754807和多西他赛耐药,但对替莫唑胺敏感。IL4I1的高表达与肿瘤的免疫抑制状态有关,可能有助于肿瘤相关巨噬细胞的侵袭。因此,IL4I1 可能是治疗和预后癌症患者的一个新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pan-cancer analysis of prognostic and immunological role of IL4I1 in human tumors: a bulk omics research and single cell sequencing validation

Pan-cancer analysis of prognostic and immunological role of IL4I1 in human tumors: a bulk omics research and single cell sequencing validation

Background

Interleukin-4 inducible gene 1 (IL4I1) regulates tumor progression in numerous tumor types. However, its correlation with immune infiltration and prognosis of patients in a pan-cancer setting remains unclear.

Methods

Data from the Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx), UALCAN, Clinical Proteomic Tumor Analysis Consortium (CPTAC), Gene Expression Omnibus (GEO), cBioPortal, Cancer Single-cell State Atlas (CancerSEA), and Tumor IMmune Estimation Resource(TIMER) databases were used to evaluate IL4I1 expression, clinical features and prognostic effects, gene set enrichment, and correlation with immune cell infiltration, as well as the relationship between IL4I1 methylation and expression and survival prognosis. Correlations with 192 anticancer drugs were also analyzed.

Results

IL4I1 was significantly overexpressed in the majority of tumors, and the imbalance of IL4I1 was significantly correlated with overall survival and pathological stage. Moreover, total IL4I1 protein was increased in cancer. Therefore, IL4I1 may be used as a prognostic biomarker or protective factor in numerous types of cancer. The methylation level of IL4I1 may also be used as a prognostic marker. The functional enrichment of IL4I1 was closely related to the immunomodulatory pathway. In addition, the level of tumor-associated macrophage infiltration was positively correlated with the expression of IL4I1 in pan-cancerous tissues. scRNA-seq analysis suggested that IL4I1 differ significantly among different cells in the tumor microenvironment and was most enriched in macrophages. Various immune checkpoint genes were positively correlated with IL4I1 expression in most tumors. In addition, patients with high IL4I1 expression may be resistant to BMS-754807 and docetaxel, but sensitive to temozolomide.

Conclusion

IL4I1 may play a role as promoter of cancer and prognostic indicator in patients. High expression of IL4I1 is associated with the state of tumor immunosuppression and may contribute to tumor-associated macrophage invasion. Therefore, IL4I1 may be a new therapeutic target for the treatment and prognosis of patients with cancer.

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