RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:TMUB1 Correlated with Immune Infiltration Is a Prognostic Marker for Colorectal Cancer.
TMUB1 Correlated with Immune Infiltration Is a Prognostic Marker for Colorectal Cancer.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
TMUB1 的高表达与 CRC 患者的不良预后密切相关。TMUB1 可能是一个潜在的预后生物标志物,并可用于 CRC 的治疗方法。
跨膜和泛素样结构域包含蛋白1(TMUB1)在大量肝脏和食管肿瘤中过表达。然而,关于TMUB1在结直肠癌(CRC)中临床意义的研究报道较少。
在此,我们通过生物信息学分析评估了TMUB1的临床意义和潜在生物学作用。采用单因素和多因素分析评估TMUB1与临床病理特征的关系。通过基因集富集分析(GSEA)确定TMUB1的生物学功能,同时使用简单样本GSEA分析TMUB1表达与24种免疫细胞浸润之间的关联。
TMUB1在CRC组织中较正常对照显著过表达。TMUB1在CRC中的高表达与T分期、新类型和残留肿瘤相关。此外,TMUB1被确定为不良无病生存期(DFS)和较短总生存期(OS)的独立因素。GSEA显示,TMUB1与缺氧、血管生成、脂肪生成、炎症反应、IL6-JAK-STAT3信号通路、凋亡、有丝分裂纺锤体及IL2-STAT5信号通路相关。TMUB1的表达与T辅助细胞、Tcm细胞、巨噬细胞和Th2细胞的丰度呈负相关,而与包括CD56bright和CD56dim NK细胞在内的多种免疫细胞类型的丰度呈正相关。
Transmembrane and ubiquitin-like domain-containing protein 1 (TMUB1) is overexpressed in a large number of liver and esophageal tumors. However, only a few reports on the clinical significance of TMUB1 in colorectal cancer (CRC) exist.
Here, we evaluated the clinical significance and potential biological role of TMUB1 using bioinformatics analysis. Univariate and multivariate analyses were performed to evaluate the relationship of TMUB1 with clinicopathological features. Gene set enrichment analysis (GSEA) was performed to identify the biological function of TMUB1, while any associations between the expression of TMUB1 and the infiltration of 24 immune cells were analyzed using simple-sample GSEA.
TMUB1 was significantly overexpressed in CRC tissues compared with normal controls. The high expression of TMUB1 in CRC was associated with T stage, neotype, and residual tumor. Moreover, TMUB1 was identified as an independent factor of poor disease-free survival (DFS) and short overall survival (OS). GSEA demonstrated that TMUB1 was related to hypoxia, angiogenesis, adipogenesis, inflammatory response, IL6-JAK-STAT3 signaling, apoptosis, mitotic spindle, and IL2-STAT5 signaling. The expression of TMUB1 negatively correlated with the abundance of T helper cells, Tcm cells, macrophages, and Th2 cells, whereas it positively correlated with the abundance of several immune cell types, including CD56bright and CD56dim NK cells.
The high expression of TMUB1 is closely related to a poor prognosis in patients with CRC. TMUB1 may be a potential prognostic biomarker and be used for therapeutic approaches in CRC.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。