RUNX基因家族在人类癌症中的预后价值和免疫特性:一项泛癌症分析

Han Zhao, Yun Chen, Peijun Shen, Lan Gong
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引用次数: 3

摘要

背景:runt相关转录因子(RUNX)参与了许多基本的生物学过程,在肿瘤发生和转移中直接或间接地起着至关重要的作用。然而,RUNX基因家族的泛癌证据尚不存在。方法:本研究基于the Cancer Genome Atlas、gene expression Omnibus和Oncomine数据库,分析RUNX基因家族表达与不同类型肿瘤患者预后、免疫细胞浸润、药物反应和基因突变数据之间的潜在关联。结果:结果显示,RUNX基因家族在不同癌症类型中的表达存在差异,揭示了其在癌症中的异质性,且RUNX2在所有癌症类型中的表达均低于RUNX1和RUNX3。RUNX基因家族基因表达与多种肿瘤的预后有关。此外,我们的研究揭示了RUNX基因家族表达与ESTIMATE评分、RNA干性和DNA干性评分之间的明确关联。与RUNX1和RUNX2相比,RUNX3的遗传改变水平相对较低。RUNX基因家族基因与免疫浸润亚型有明显的关联,其表达在多数情况下与免疫检查点基因和药物敏感性呈正相关。两个免疫治疗队列证实RUNX的表达与免疫治疗的临床反应相关。结论:这些发现有助于阐明RUNX基因家族基因在不同类型肿瘤中的潜在致癌作用,并可作为各种恶性肿瘤的预后标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic value and immune characteristics of RUNX gene family in human cancers: a pan-cancer analysis
Background: Runt-related transcription factors (RUNX) are involved in numerous fundamental biological processes and play crucial parts in tumorigenesis and metastasis both directly and indirectly. However, the pan-cancer evidence of the RUNX gene family is not available. Methods: In this study, we analyzed the potential association between RUNX gene family expression and patient’s prognosis, immune cell infiltration, drug response, and genetic mutation data across different types of tumors using based on The Cancer Genome Atlas, Gene Expression Omnibus, and Oncomine database. Results: The results showed that the expression of the RUNX gene family varied among different cancer types, revealing its heterogeneity in cancers and that expression of RUNX2 was lower than that of RUNX1 and RUNX3 across all cancer types. RUNX gene family gene expression was related to prognosis in several cancers. Furthermore, our study revealed a clear association between RUNX gene family expression and ESTIMATE score, RNA stemness, and DNA stemness scores. Compared with RUNX1 and RUNX2, RUNX3 showed relatively low levels of genetic alterations. RUNX gene family genes had clear associations with immune infiltrate subtypes, and their expression was positively related to immune checkpoint genes and drug sensitivity in most cases. Two immunotherapy cohorts confirm that the expression of RUNX was correlated with the clinical response of immunotherapy. Conclusions: These findings will help to elucidate the potential oncogenic roles of RUNX gene family genes in different types of cancer and it can function as a prognostic marker in various malignant tumors.
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