Head and neck squamous cell carcinoma (HNSCC) develops within a chronically inflamed and metabolically constrained tumor microenvironment that profoundly shapes innate immune function. Tumor-associated macrophages (TAMs) are abundant in HNSCC and display marked plasticity, yet predominantly acquire immunosuppressive states that promote tumor progression and therapeutic resistance. Traditional M1/M2 polarization models fail to capture this dynamic behavior. Emerging evidence instead identifies metabolic reprogramming as a central regulator of macrophage function in cancer. Hypoxia, nutrient limitation, extracellular acidification, and tumor-derived metabolites such as lactate and lipids rewire macrophage metabolism, directly influencing inflammatory signaling and immune suppression. This review integrates recent advances in immunometabolism to examine how metabolic adaptations govern macrophage innate functions in HNSCC and highlights therapeutic opportunities targeting macrophage metabolism to overcome immune resistance.
Building similarity graph...
Analyzing shared references across papers
Loading...
Vincent Yuan (Tue,) studied this question.
www.synapsesocial.com/papers/69d0af52659487ece0fa5351 — DOI: https://doi.org/10.3390/biology15070561
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Vincent Yuan
Biology
University of Pittsburgh Medical Center
Building similarity graph...
Analyzing shared references across papers
Loading...