Neutrophil polarization landscapes in HCC: From immunosuppressive niches to antitumor immunity resuscitation

免疫学 医学 免疫 复苏 免疫系统 中性粒细胞 免疫抑制 中性粒细胞胞外陷阱 细胞免疫 生物 癌症研究 利基 生态位 炎症 免疫疗法 先天免疫系统 获得性免疫系统
作者
Jun Sun,Fan Yang,Yinyan Li,Shenglong Li,Jianbo Song
出处
期刊:Cancer Letters [Elsevier BV]
卷期号:651: 218527-218527 被引量:1
标识
DOI:10.1016/j.canlet.2026.218527
摘要

Hepatocellular carcinoma (HCC) is a leading cause of global cancer mortality, arising predominantly in the context of chronic liver injury and cirrhosis. The tumor microenvironment (TME) is a critical orchestrator of HCC progression and therapeutic resistance. Neutrophils, the most abundant circulating leukocytes and key first responders in hepatic immunity, play a pivotal and multifaceted role in this process. Under physiological conditions, neutrophils are essential for liver homeostasis and acute injury resolution. However, across the pathological continuum from chronic liver disease to HCC, sustained inflammatory signaling drives a profound reprogramming of neutrophil function. Within the established HCC TME, tumor-associated neutrophils (TANs) are frequently polarized into a protumorigenic phenotype, actively driving disease progression through several core mechanisms: they establish immunosuppressive niches by directly suppressing cytotoxic T-cell function; promote angiogenesis and metastasis via the secretion of factors like VEGF and MMPs; and contribute to genomic instability and therapy resistance through mechanisms such as neutrophil extracellular trap (NET) formation. This functional transition from defenders in acute injury to accomplices in malignant progression underscores the central role of neutrophils in liver pathobiology and HCC pathogenesis. This review synthesizes current knowledge on the recruitment, polarization, and functional diversity of neutrophils in the HCC TME, with a particular focus on their mechanisms in mediating immunosuppression through cellular crosstalk and metabolic reprogramming. We further critically evaluate emerging therapeutic strategies that target neutrophil-centric pathways to resuscitate antitumor immunity, including TAN repolarization, depletion of specific subsets, or functional blockade. Finally, we discuss the translational potential of neutrophil-related biomarkers for patient stratification and the rationale for developing combination therapies. A deeper understanding of the dynamic and pleiotropic roles of neutrophils in HCC is essential for devising more effective immunotherapeutic strategies and improving patient outcomes.
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