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:Analysis of the correlation between COL11A1 gene expression and clinical features in bladder urothelial carcinoma.
Analysis of the correlation between COL11A1 gene expression and clinical features in bladder urothelial carcinoma.
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膀胱尿路上皮癌(BLCA)是一种常见的泌尿系统恶性肿瘤,其诊断和治疗较为复杂。本研究通过分析COL11A1与临床病理特征、肿瘤进展及免疫浸润动态的关联,探讨该基因在肿瘤进展和免疫调节中的诊断及预后价值。采用Kaplan-Meier生存分析和免疫浸润分析等统计方法,我们评估了407例BLCA患者和28例正常对照中COL11A1的表达。
结果显示,BLCA组织中COL11A1显著过表达(P < 0.001),且高表达与较差的生存结局相关(风险比 = 1.53,P = 0.005)。免疫浸润分析显示,COL11A1水平与巨噬细胞、Th1细胞、自然杀伤(NK)细胞和中性粒细胞呈显著正相关(P < 0.001),同时与晚期T分期(P < 0.001)和N分期(P = 0.030)显著相关。这些发现确立了COL11A1作为BLCA多层面生物标志物的地位,为诊断、预后和治疗策略提供了重要见解。
进一步研究应阐明其在肿瘤发生和免疫调节中的机制作用,并探索其跨恶性肿瘤的应用潜力,以推动个性化肿瘤学的发展。
Bladder urothelial carcinoma (BLCA) is a prevalent urinary malignancy that complicates diagnosis and treatment.
This study investigates the diagnostic and prognostic utility of COL11A1, a gene implicated in tumor progression and immune modulation, by analyzing its association with clinicopathological features, tumor progression, and immune infiltration dynamics. Using statistical methods, including Kaplan-Meier survival analysis and immune infiltration profiling, we evaluated COL11A1 expression in 407 BLCA patients and 28 normal controls.
Results demonstrated significant COL11A1 overexpression in BLCA tissues versus controls (P < 0. 001), with elevated expression correlating with poorer survival outcomes (hazard ratio = 1. 53, P = 0. 005). Immune infiltration analysis revealed robust positive associations between COL11A1 levels and macrophages, Th1 cells, natural killer (NK) cells, and neutrophils (P < 0. 001), alongside significant links to advanced T stage (P < 0. 001) and N stage (P = 0. 030).
These findings establish COL11A1 as a multifaceted biomarker for BLCA, offering critical insights into diagnosis, prognosis, and therapeutic strategies.
Further research should elucidate its mechanistic roles in tumorigenesis and immune regulation, with potential applications across malignancies to advance personalized oncology.
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