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:Bioinformatics analysis for the identification of Sprouty-related EVH1 domain-containing protein 3 expression and its clinical significance in thyroid carcinoma.
Bioinformatics analysis for the identification of Sprouty-related EVH1 domain-containing protein 3 expression and its clinical significance in thyroid carcinoma.
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低分化甲状腺癌(THCA)亚型与侵袭性病程、较差的总体预后以及远处器官转移风险增加相关。在本研究中,我们的目标是探索Sprouty相关EVH1结构域蛋白3(SPRED3)作为THCA患者早期诊断和预后生物标志物的潜在价值。通过查询癌症基因组图谱(TCGA)数据库,鉴定了与THCA相关的差异表达预后相关基因。利用癌症基因组图谱(TCGA)的数据分析了SPRED3基因在甲状腺癌(THCA)组织与正常组织中的表达差异,并通过免疫组织化学进一步验证。使用单因素和多因素Cox回归模型,结合THCA患者的临床信息,分析SPRED3基因在THCA患者中的预后价值。随后进行功能富集分析,以阐明SPRED3基因对甲状腺癌调控作用的分子机制。
此外,我们计算了THCA患者中浸润免疫细胞的百分比,并评估其与SPRED3基因表达的相关性。与非癌性甲状腺组织相比,SPRED3在甲状腺癌组织中的基因和蛋白表达水平升高。
此外,SPRED3在甲状腺癌中的表达与肿瘤位置、组织学分级、病理分期和肿瘤淋巴结转移分类(TNM)分期呈显著相关。单因素和多因素Cox比例风险(Cox)回归分析表明,SPRED3可作为预测THCA患者总生存期的独立预后因素。功能富集分析结果提示,SPRED3可能参与细胞外基质组织、表皮发育、信号受体激活因子活性、皮肤发育、受体配体活性、糖胺聚糖结合、神经活性配体-受体相互作用、IL-17信号通路和PI3K-Akt信号通路的调控。
此外,SPRED3基因的表达水平与甲状腺肿瘤微环境中多种免疫细胞(嗜酸性粒细胞、中枢记忆T细胞、中性粒细胞、巨噬细胞和NK细胞)的浸润之间存在显著相关性。SPRED3可作为THCA患者的预后生物标志物,并可能成为THCA的治疗靶点。
The poorly differentiated thyroid carcinoma (THCA) subtype is associated with an aggressive disease course, a less favorable overall prognosis, and an increased risk of distant organ metastasis. In this study, our objective was to explore the potential utility of the Sprouty-related EVH1 domain-containing protein 3 (SPRED3) as a biomarker for early diagnosis and prognosis in THCA patients. The differentially expressed prognostic-related genes associated with THCA were identified by querying The Cancer Genome Atlas (TCGA) database.
The difference in the expression of the SPRED3 gene between thyroid carcinoma (THCA) tissues and normal tissues was analyzed using data from The Cancer Genome Atlas (TCGA) and further validated through immunohistochemistry.
Univariate and multivariate Cox regression models were used, along with clinical information from THCA patients, to analyze the prognostic value of the SPRED3 gene in THCA patients. Functional enrichment analysis was subsequently performed to elucidate the molecular mechanisms underlying the regulatory effects of the SPRED3 gene on thyroid carcinoma.
Additionally, we calculated the percentage of infiltrating immune cells in THCA patients and evaluated their correlation with SPRED3 gene expression. Compared with those in noncancerous thyroid tissue, the gene and protein expression levels of SPRED3 were found to be elevated in thyroid carcinoma tissues.
Furthermore, the expression of SPRED3 in thyroid carcinoma exhibited significant correlations with tumor location, histological grade, pathological stage, and tumor node metastasis classification (TNM) stage. Univariate and multivariate Cox proportional hazards (Cox) regression analyses demonstrated that SPRED3 could serve as an independent prognostic factor for predicting the overall survival of THCA patients.
The results of functional enrichment analysis suggested the potential involvement of SPRED3 in the regulation of extracellular matrix organization, epidermal development, signaling receptor activator activity, skin development, receptor ligand activity, glycosaminoglycan binding, neuroactive ligand‒receptor interaction, the IL-17 signaling pathway, and the PI3K-Akt signaling pathway.
Additionally, there were significant correlations between the expression level of the SPRED3 gene and the infiltration of various immune cells (eosinophils, central memory T cells, neutrophils, macrophages, and NK cells) within the thyroid tumor microenvironment. SPRED3 can be used as a prognostic biomarker in patients with THCA could potentially be therapeutic target for THCA.
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