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:C16orf74 is a novel prognostic biomarker and associates with immune infiltration in head and neck squamous cell carcinoma.
C16orf74 is a novel prognostic biomarker and associates with immune infiltration in head and neck squamous cell carcinoma.
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。
头颈部鳞状细胞癌(HNSC)是一种常见且侵袭性强的恶性肿瘤,预后较差,凸显了对新型生物标志物和治疗策略的需求。本研究探讨了C16orf74作为HNSC潜在诊断和预后生物标志物的作用。生物信息学分析显示,C16orf74在HNSC中显著过表达,并与疾病晚期、治疗耐药以及较短的总生存期和无进展生存期相关。整合C16orf74表达与临床病理特征构建的预后列线图展现出稳健的预测性能。功能富集和免疫浸润分析表明,C16orf74高表达可能通过减少关键免疫细胞群体(如B细胞、T细胞和NK 细胞)而促进免疫抑制性肿瘤微环境,这些细胞对抗肿瘤免疫至关重要。
此外,C16orf74表达与免疫检查点表达及免疫治疗反应呈负相关,凸显其作为免疫检查点阻断(ICB)疗效预测生物标志物的潜力。药物敏感性分析确定了针对C16orf74高表达患者的潜在治疗药物,包括三氧化二砷、卡莫司汀、长春新碱、槲皮素和卡铂。这些发现凸显了C16orf74作为生物标志物和治疗靶点以改善HNSC管理的潜力。
Head and neck squamous cell carcinoma (HNSC) is a prevalent and aggressive malignancy with poor prognosis, underscoring the need for novel biomarkers and therapeutic strategies.
This study investigates the role of C16orf74 as a potential diagnostic and prognostic biomarker in HNSC. Bioinformatics analyses revealed that C16orf74 is significantly overexpressed in HNSC and is associated with advanced disease stages, therapy resistance, and shorter overall and progression-free survival.
A prognostic nomogram integrating C16orf74 expression with clinicopathological features demonstrated robust predictive performance. Functional enrichment and immune infiltration analyses suggest that high C16orf74 expression might contribute to an immunosuppressive tumor microenvironment by reducing key immune cell populations, such as B cells, T cells, and natural killer cells, which are critical for anti-tumor immunity.
Moreover, C16orf74 expression was inversely associated with immune checkpoint expression and immunotherapy response, highlighting its potential as a predictive biomarker for immune checkpoint blockade (ICB) efficacy. Drug sensitivity analyses identified potential therapeutic agents, including arsenic trioxide, carmustine, vincristine, quercetin, and carboplatin for patients with high C16orf74 expression.
These findings highlight the potential of C16orf74 as a biomarker and therapeutic target to improve HNSC management.
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。