胸腺瘤预后的一种新的免疫相关microRNA标记

Bin Wang, He Xiao, Xin Yang, Ying Zeng, Zhimin Zhang, Rui Yang, Hang Chen, Chuan Chen, Junxia Chen
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引用次数: 4

摘要

免疫微环境和microrna是肿瘤诊断和预后的常用预测因子。方法:从TCGA数据库中获取胸腺瘤组织中122个基因和126个microrna的表达。计算肿瘤浸润细胞比例,构建IMRS。在对基因集进行功能富集分析之前,计算TREM2hi评分。结果:IMRS3、TREM2hi评分、CD8+ T淋巴细胞丰度在WHO分类中存在显著差异。WHO分级、Masaoka分期以及miR-130b-5p、miR-1307-3p、miR-425-5p、CD8、CD68和CCL18的表达是无复发生存期和总生存期的预后因素。IMRS3上调使巨噬细胞极化进入M2,排斥CD8+ T等效应淋巴细胞,促进胸腺瘤恶性进展。结论:BRRS可能是TET预后的一种新的免疫相关microRNA特征。
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A novel immune-related microRNA signature for prognosis of thymoma
Introduction: Immune microenvironment and microRNAs serve as common predictors for diagnosis and prognosis of tumors. Methods: Expression of 122 genes and 126 microRNAs in thymoma was obtained from TCGA database. The proportion of tumor-infiltrating cells was calculated, and IMRS was constructed. TREM2hi score was calculated before functional enrichment analysis on gene sets. Results: IMRS3, TREM2hi score, and CD8+ T lymphocyte abundance were significantly different among WHO classifications. WHO classification, Masaoka staging, and miR-130b-5p, miR-1307-3p, miR-425-5p, CD8, CD68, and CCL18 expression were prognostic factors for relapse-free survival and overall survival. IMRS3 upregulation polarized macrophages into M2, which rejected CD8+ T and other effector lymphocytes to promote thymoma malignant progression. Conclusions: BRRS may present a novel immune-related microRNA signature for TET prognosis.
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