通过NETs-IL-17/VEGF/S100A9轴的中性细胞-巨细胞交叉促进肝细胞癌的进展
Rong Wu1, Rui Wu2, Xuehua Kong1
1Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, No.74 linjiang Road, Yu Zhong District, Chongqing, 400010, China.
Journal of experimental & clinical cancer research : CR
|December 31, 2025
概括
中性细胞外细胞陷 (NETs) 和IL-17通过重编程巨细胞来驱动肝细胞癌 (HCC) 的进展和转移. NETs-IL-17显示为预测HCC转移的生物标志物具有前途.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 癌症生物学 癌症生物学
背景情况:
- 与瘤相关的中性粒细胞和巨细胞在肝细胞癌 (HCC) 微环境中至关重要.
- 这些细胞之间的精确相互作用及其在HCC进展中的作用尚未完全理解.
研究的目的:
- 研究中性粒细胞外细胞陷 (NETs) 中介的巨细胞重编程在HCC.中的机制.
- 阐明这种相互作用对HCC进展和转移的贡献.
主要方法:
- 对TCGA和临床HCC样本的生物信息分析.
- 与中性粒细胞,巨细胞和HCC细胞进行共同培养实验.
- 在体内小鼠模型和分子分析.
主要成果:
- 在HCC中,NETs升高,与M2巨细胞透和前转移性细胞因子相关.
- NETs通过IL-17/IL-17R/NF-κB信号传递诱导M2d巨分化,增强瘤生长,血管新生和转移.
- 确定了中性粒细胞和M2d巨细胞之间的积极反循环,涉及NETs-IL-17,VEGF和S100A9.
- NETs-IL-17显示了肝外转移的高预测值 (AUC=0.89).
结论:
- 一个NETs-IL-17/VEGF/S100A9轴创建一个积极的反循环,加速HCC的进展和转移.
- NETs-IL-17是一种潜在的生物标志物,可用于预测HCC的肝外转移.
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