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:The role of lnc‑MAPKAPK5‑AS1 in immune cell infiltration in hepatocellular carcinoma: Bioinformatics analysis and validation.
The role of lnc‑MAPKAPK5‑AS1 in immune cell infiltration in hepatocellular carcinoma: Bioinformatics analysis and validation.
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lnc-MAPKAPK5-AS1在多种癌症中的致癌和抑癌作用表明其在调节癌症进展中的复杂性。通过从The Cancer Genome Atlas和Gene Expression Omnibus进行数据挖掘,研究了lnc-MAPKAPK5-AS1在肝细胞癌(HCC)中的表达和启动子甲基化水平,并探讨了其在预后和免疫中的意义。lnc-MAPKAPK5-AS1在HCC中与其蛋白编码基因MAPKAPK5共表达,并由于其启动子区域低甲基化而在HCC组织中表现出上调。lnc-MAPKAPK5-AS1高表达与不良预后相关。富集分析显示,lnc-MAPKAPK5-AS1参与免疫和代谢相关通路。lnc-MAPKAPK5-AS1表达的变化影响肿瘤微环境中的浆细胞、T细胞CD4 +记忆静息细胞、NK细胞、巨噬细胞M0/M1和静息肥大细胞。
发现lnc-MAPKAPK5-AS1与多个免疫检查点相关。对Sangerbox数据库的分析显示,lnc-MAPKAPK5-AS1表达、肿瘤突变负荷和微卫星不稳定性之间存在正相关关系,这提示免疫治疗可能在lnc-MAPKAPK5-AS1高表达的肿瘤中有效。经验证,lnc-MAPKAPK5-AS1的表达可指示对16种常见靶向药物的敏感性。免疫组织化学证实了MAPKAPK5蛋白在HCC中的表达及其预后意义。应用加权基因共表达网络分析来识别与免疫反应评分和基因表达均相关的枢纽基因。这些结果表明,lnc-MAPKAPK5-AS1可能作为癌基因参与HCC的发生发展,并可能通过调节物质代谢和免疫反应成为潜在的治疗靶点。
The oncogenic and tumor suppressor roles of lnc-MAPKAPK5-AS1 in multiple cancers suggest its complexity in modulating cancer progression. The expression and promoter methylation level of lnc-MAPKAPK5-AS1 in hepatocellular carcinoma (HCC) was investigated through data mining from The Cancer Genome Atlas and Gene Expression Omnibus and its significance in prognosis and immunity was explored. lnc-MAPKAPK5-AS1 was co-expressed with its protein-coding gene MAPKAPK5 in HCC and exhibited upregulation in HCC tissues as a result of hypomethylation of its promoter region. High expression of lnc-MAPKAPK5-AS1 was associated with poor prognosis. Enrichment analysis revealed that lnc-MAPKAPK5-AS1 is involved in immune and metabolic-related pathways. Changes in the expression of lnc-MAPKAPK5-AS1 affected plasma cells, T cells CD4 + memory resting, NK cells, macrophages M0/M1, and mast cells resting in the tumor microenvironment.
lnc-MAPKAPK5-AS1 was found to correlate with multiple immune checkpoints. Analysis of the Sangerbox database revealed positive relationships between expression of lnc-MAPKAPK5-AS1, tumor mutational burden and microsatellite instability, which suggested that immunotherapy may be effective in tumors with high expression of lnc-MAPKAPK5-AS1. The expression of lnc-MAPKAPK5-AS1 was verified to indicate sensitivity to 16 common targeted drugs.
Immunohistochemistry confirmed the expression of MAPKAPK5 protein in HCC and its prognostic significance. Weighted gene co-expression network analysis was applied to identify hub genes related to both immunoreactive score and gene expression. These results revealed that lnc-MAPKAPK5-AS1 may be involved in the occurrence and development of HCC as an oncogene and may represent a potential therapeutic target through modulating the substance metabolism and immune response.
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