Wang Qinghao, Zhang Zixin, Zhou Hao, Qin Yanling, He Jun, Li Limin, Ding Xiaofeng
The National & Local Joint Engineering Laboratory of Animal Peptide Drug Development, College of Life Science, Hunan Normal University, Changsha, 410081, China.
Institute of Interdisciplinary Studies, Hunan Normal University, Changsha, 410081, China.
J Cancer. 2024 Sep 3;15(17):5605-5621. doi: 10.7150/jca.95138. eCollection 2024.
Eosinophils, a type of white blood cell originating from the bone marrow, are widely believed to play a crucial role in inflammatory processes, including allergic reactions and parasitic infections. However, the relationship between eosinophils and liver cancer is not well understood. Tumor immune infiltration scores were calculated using single-sample Gene Set Enrichment Analysis (ssGSEA). Key modules and hub genes associated with eosinophils were screened using Weighted Gene Co-expression Network Analysis (WGCNA). Univariate and multivariate Cox analyses, along with LASSO regression, were used to identify prognostic genes and create a risk model. The Tumor Immune Dysfunction and Exclusion (TIDE) score was used to evaluate the immunotherapeutic significance of the eosinophil-associated gene risk score (ERS) model. Experiments such as flow cytometry, immunohistochemical analysis, real-time quantitative PCR (RT-qPCR), and Western blotting were used to determine gene expression levels and the status of eosinophil infiltration in tumors. A risk trait model including 4 eosinophil-associated genes (RAMP3, G6PD, SSRP1, PLOD2) was developed by univariate Cox analysis and Lasso screening. Pathologic grading (p < 0.001) and model risk scores (p < 0.001) were found to be independent predictors of hepatocellular carcinoma (HCC) patient survival. Western blotting revealed higher levels of eosinophil peroxidase (EPX) in HCC tissues compared to adjacent normal tissues. Immunohistochemistry showed that eosinophils mainly infiltrated the connective tissue around HCC. The HCC samples showed low expression of RAMP3 and high expression of G6PD, SSRP1, and PLOD2, as detected by IHC and RT-qPCR analysis. The mouse experiments showed that IL-33 treatment induced the recruitment of eosinophils and reduced the number of intrahepatic tumor nodules. Overall, eosinophil infiltration in HCC is significantly correlated with patient survival. The risk assessment model based on eosinophil-related genes serves as a reliable clinical prognostic indicator and provides insights for precise treatment of HCC.
嗜酸性粒细胞是一种起源于骨髓的白细胞,人们普遍认为它在炎症过程中发挥关键作用,包括过敏反应和寄生虫感染。然而,嗜酸性粒细胞与肝癌之间的关系尚未完全明确。使用单样本基因集富集分析(ssGSEA)计算肿瘤免疫浸润评分。使用加权基因共表达网络分析(WGCNA)筛选与嗜酸性粒细胞相关的关键模块和枢纽基因。单变量和多变量Cox分析以及LASSO回归用于识别预后基因并创建风险模型。肿瘤免疫功能障碍和排除(TIDE)评分用于评估嗜酸性粒细胞相关基因风险评分(ERS)模型的免疫治疗意义。通过流式细胞术、免疫组织化学分析、实时定量PCR(RT-qPCR)和蛋白质免疫印迹等实验来确定基因表达水平以及肿瘤中嗜酸性粒细胞浸润情况。通过单变量Cox分析和LASSO筛选,建立了一个包含4个嗜酸性粒细胞相关基因(RAMP3、G6PD、SSRP1、PLOD2)的风险特征模型。病理分级(p < 0.001)和模型风险评分(p < 0.001)被发现是肝细胞癌(HCC)患者生存的独立预测因素。蛋白质免疫印迹显示,与相邻正常组织相比,HCC组织中嗜酸性粒细胞过氧化物酶(EPX)水平更高。免疫组织化学显示,嗜酸性粒细胞主要浸润HCC周围的结缔组织。免疫组织化学和RT-qPCR分析检测到,HCC样本中RAMP3表达低,G6PD、SSRP1和PLOD2表达高。小鼠实验表明,IL-33治疗可诱导嗜酸性粒细胞募集并减少肝内肿瘤结节数量。总体而言,HCC中的嗜酸性粒细胞浸润与患者生存显著相关。基于嗜酸性粒细胞相关基因的风险评估模型可作为可靠的临床预后指标,并为HCC的精准治疗提供思路。