Beta-glucans, naturally occurring polysaccharides derived from fungi, yeasts, cereals, and bacteria, have emerged as potent cancer therapeutics due to their multifaceted immunomodulatory, anti-inflammatory, and direct anti-tumor properties. These compounds engage pattern recognition receptors (PRRs) such as Dectin-1, Toll-like receptors (TLRs), and complement receptor 3 (CR3), activating macrophages, natural killer (NK) cells, and dendritic cells to enhance anti-tumor immunity. Beta-glucans suppress pro-inflammatory cytokines (e.g., TNF-α, IL-6) and tumor-promoting pathways like NF-κB, while modulating gut microbiota to create an anti-cancer environment. Their nanoparticle formulations enable targeted drug delivery, enhancing the efficacy of chemotherapy and immunotherapy. Clinical studies demonstrate their synergy with cancer treatments, improving patient outcomes and quality of life.
This 2025 review comprehensively covers β-glucan mechanisms in oncology: receptor engagement (Dectin-1, TLR, CR3), immune cell activation (macrophages, NK cells, DCs), NF-κB suppression, gut microbiota modulation, and nanoparticle-based drug delivery. Clinical evidence confirms synergy with chemotherapy and immunotherapy. The review positions β-glucans as versatile cancer immunotherapy adjuvants with multi-pronged mechanisms against tumor growth and immune evasion.
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Ameri Shah Reza M; Najafi S; Kahfi M; Safari M; Mahjoor M. Beta-glucans in oncology: revolutionizing treatment with immune power & tumor targeting. Naunyn-Schmiedeberg's Archives of Pharmacology. 2025. DOI: 10.1007/s00210-025-04519-8. PMID: 40864254.
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