神经肽肾上腺髓质素通过负性调节肿瘤免疫促进头颈部鳞状癌的进展

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摘要

目的:探讨神经肽基因肾上腺髓质素(ADM)在头颈部鳞状细胞癌(HNSC)中的调节机制和功能。方法:利用TCGA-HNSC数据库公开的数据,通过分析ADM的RNA表达水平,探讨ADM单基因在HNSC中的作用,特别从肿瘤浸润性免疫细胞、免疫调节基因、免疫检查点基因、estimat - immune - stromal评分、免疫簇预后价值等方面探讨ADM在肿瘤免疫中的作用。使用R软件包对癌症和非癌症样本的数据进行统计分析。在本分析中使用了许多web服务器,包括cBioportal, TIMER, STRING, GeneMANIA和GEPIA。结果:在HNSC肿瘤样本中发现ADM显著上调,并与较差的预后结果相关。在HNSC中,adm显著相关基因在细胞因子-细胞因子受体相互作用、HIF-1信号转导、MAPK信号转导、趋化因子信号转导、AGE-RAGE信号转导、松弛素信号转导、病毒蛋白与细胞因子和细胞因子受体相互作用、nf - κ B信号转导等多种促瘤通路中富集。ADM与肿瘤巨噬细胞、T细胞、B细胞、Treg细胞、T辅助细胞、Th17细胞、NK细胞、肥大细胞、树突状细胞等多种浸润性免疫细胞呈负相关,参与HNSC的肿瘤免疫。ADM的表达与大部分免疫调节基因呈负相关。在HNSC中,ADM与estimate_stromal - immune评分呈负相关,提示其参与肿瘤免疫微环境。结论:ADM基因可能通过负调控免疫细胞、介导细胞因子和趋化因子信号通路、HIF-1信号通路、MAPK信号通路、nf - κ B信号通路,在HNSC的进展中发挥重要作用。因此,ADM可作为一种有价值的候选生物标志物,在头颈部肿瘤的治疗中具有广阔的应用前景。
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The neuropeptide Adrenomedullin Promoted the Progression of Head and Neck Squamous Carcinoma by Negatively Regulating Tumour Immunity
Objective: To investigate the putative regulatory mechanisms and functions of the neuropeptide gene adrenomedullin (ADM) in head and neck squamous cell carcinoma (HNSC). Methods: Publicly available data from the TCGA-HNSC database were utilized to explore the involvement of ADM single gene in HNSC by analyzing RNA expression levels of ADM. The involvement of ADM in tumor immunity was particularly investigated from the aspect of tumor-infiltrating immune cells, immune modulator genes, immune checkpoint genes, Estimate-Immune-Stromal score, and immune clusters’ prognostic values. Statistical analysis of the data pertaining to cancer and non-cancerous samples was performed using R software packages. Many web servers were used in the present analyses, including cBioportal, TIMER, STRING, GeneMANIA, and GEPIA. Results: ADM was found to be significantly upregulated in HNSC tumor samples and associated with worse prognostic outcomes. ADM-significantly correlated genes in HNSC were enriched in several tumor promoting pathways, including cytokine-cytokine receptor interaction, HIF-1 signaling, MAPK signaling, chemokine signaling, AGE-RAGE signaling, Relaxin signaling, viral protein interaction with cytokine and cytokine receptor, and NF-kappa B signaling. ADM is involved in tumor immunity of HNSC by being negatively correlated with several tumor-infiltrating immune cells, including tumor macrophages, T cells, B cells, Treg cells, T helper cells, Th17 cells, NK cells, mast cells, and dendritic cells. The negative correlation was observed between ADM expression and the majority of immunomodulator genes. ADM was also found to be negatively correlated with the Estimate-Stromal-Immune score in HNSC, indicating its involvement in the tumor immune microenvironment. Conclusions: ADM gene may play a significant role in promoting the progression of HNSC by negatively regulating immune cells, mediating cytokine and chemokine signaling, HIF-1 signaling, MAPK signaling, and NF-kappa B signaling. Therefore ADM can be regarded as a valuable candidate biomarker and holds promising prospects in treating head and neck cancer.
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