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:Epigenetic Regulation of NKT-Cell-Related Gene Signatures and Prognostic Implications in Oropharyngeal Squamous Cell Carcinoma.
Epigenetic Regulation of NKT-Cell-Related Gene Signatures and Prognostic Implications in Oropharyngeal Squamous Cell Carcinoma.
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这些发现凸显了 NKT 细胞分化在 OPSCC 中是一个强有力的预后指标,并支持进一步探索表观遗传-免疫相互作用作为潜在治疗靶点。
口咽鳞状细胞癌(OPSCC)是头颈癌的主要亚型,其预后日益受到肿瘤免疫微环境的影响。尽管免疫检查点抑制剂已改善部分患者的结局,但可靠的预测性生物标志物仍然有限。
本研究旨在探讨OPSCC中自然杀伤T(NKT)细胞相关基因特征的预后相关性及表观遗传调控。采用单样本基因集富集分析(ssGSEA)对81例OPSCC患者的临床病理和转录组数据进行分析,以评估免疫相关基因集富集评分。评估了其与总生存期和临床特征的关联,并通过表达、甲基化和网络分析进一步探索了候选预后基因。
高NKT细胞分化富集评分与生存改善和有利的临床特征显著相关。基因水平分析确定ITK、ZNF683和ATF2是与T细胞信号传导和表观遗传调控相关的关键预后标志物。甲基化谱分析显示肿瘤组织中ITK高甲基化和ZNF683低甲基化,提示基因表达改变的表观遗传基础。
Oropharyngeal squamous cell carcinoma (OPSCC) is a major subtype of head and neck cancer, with prognosis increasingly influenced by the tumour immune microenvironment. Although immune checkpoint inhibitors have improved outcomes for some patients, reliable predictive biomarkers remain limited.
This study aimed to investigate the prognostic relevance and epigenetic regulation of natural killer T (NKT)-cell-related gene signatures in OPSCC. Clinicopathological and transcriptomic data from 81 OPSCC patients were analysed using single-sample gene set enrichment analysis (ssGSEA) to evaluate immune-related gene set enrichment scores. Associations with overall survival and clinical features were assessed, and candidate prognostic genes were further explored through expression, methylation, and network analyses.
High NKT cell differentiation enrichment scores were significantly associated with improved survival and favourable clinical features. Gene-level analyses identified ITK, ZNF683, and ATF2 as key prognostic markers linked to T-cell signalling and epigenetic regulation. Methylation profiling revealed hypermethylation of ITK and hypomethylation of ZNF683 in tumour tissues, suggesting an epigenetic basis for altered gene expression.
These findings highlight NKT cell differentiation as a strong prognostic indicator in OPSCC and support further exploration of epigenetic-immunologic interactions as potential therapeutic targets.
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