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GNGT1是胃癌中一种潜在的预后和免疫生物标志物。

GNGT1 is a potential prognostic and immunologic biomarker in gastric cancer.

作者信息

Huang Xuchong, Lin Juan, Wang Jian, Yang Weifeng, Ou Wenquan, Huang Xing, Chen Jiahua, Zhang Zixing, Wu Xiaohua

机构信息

Department of Clinical Medicine, Fujian Medical University, Fuzhou, China.

Department of General Surgery, Nanping First Hospital Affiliated to Fujian Medical University, Nanping, China.

出版信息

Sci Rep. 2025 Jul 1;15(1):21149. doi: 10.1038/s41598-025-08297-4.

Abstract

Gastric cancer(GC) is the fifth most common type of cancer worldwide and ranks third in terms of cancer-related mortality. Immunotherapy has shown promising outcomes and greatly extended survival in individuals with advanced stomach cancer. To improve the immunotherapy response in patients with GC, it is necessary to discover new molecular targets. The associations among G protein subunit gamma transducin 1(GNGT1) expression, clinicopathological features, and prognosis were assessed via the UALCAN and Kaplan-Meier databases. The CIBERSORT algorithm in R software and single-sample gene set enrichment analysis(ssGSEA) were used to analyse the proportions of infiltrating immune cells in the high-expression group and the low-expression group.GNGT1 expression was substantially greater in GC tissues than in normal tissues, and patients with GC who had high GNGT1 expression had worse clinicopathological characteristics and survival outcomes. Immunohistochemistry(IHC) experiments on stomach adenocarcinoma(STAD) samples confirmed the aberrant expression of GNGT1 and its association with a poor prognosis. Subsequent investigations revealed substantial negative correlations between GNGT1 and tumour mutational burden(TMB), microsatellite instability(MSI), immune cell infiltration, immune cell gene marker expression and immunological checkpoint expression in patients with STAD.GNGT1 is a reliable biomarker in patients with GC that also has an immunomodulatory function in this disease and may accelerate GC development by suppressing the infiltration of T cells, dendritic cells, M1 macrophages and B cells.

摘要

胃癌(GC)是全球第五大常见癌症类型,在癌症相关死亡率方面排名第三。免疫疗法已显示出有前景的结果,并极大地延长了晚期胃癌患者的生存期。为了提高GC患者的免疫治疗反应,有必要发现新的分子靶点。通过UALCAN和Kaplan-Meier数据库评估了G蛋白亚基γ转导素1(GNGT1)表达、临床病理特征和预后之间的关联。使用R软件中的CIBERSORT算法和单样本基因集富集分析(ssGSEA)来分析高表达组和低表达组中浸润免疫细胞的比例。GNGT1在GC组织中的表达明显高于正常组织,GNGT1高表达的GC患者具有更差的临床病理特征和生存结果。对胃腺癌(STAD)样本进行的免疫组织化学(IHC)实验证实了GNGT1的异常表达及其与不良预后的关联。随后的研究揭示了STAD患者中GNGT1与肿瘤突变负荷(TMB)、微卫星不稳定性(MSI)、免疫细胞浸润、免疫细胞基因标志物表达和免疫检查点表达之间存在显著的负相关。GNGT1是GC患者的可靠生物标志物,在该疾病中也具有免疫调节功能,并且可能通过抑制T细胞、树突状细胞、M1巨噬细胞和B细胞的浸润来加速GC的发展。

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