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结肠癌免疫治疗中的肿瘤相关巨噬细胞:作用机制、天然产物干预及微环境重塑

Tumor-associated macrophages in colon cancer immunotherapy: mechanisms, natural product interventions, and microenvironment remodeling.

作者信息

He Qingman, Xiang Li, Luo Yuanyuan, Wang Rongrong, Zheng Chuan, Gao Yongxiang, Yao Huan

机构信息

Department of Rheumatology and Immunology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.

College of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.

出版信息

Front Immunol. 2025 Aug 12;16:1642091. doi: 10.3389/fimmu.2025.1642091. eCollection 2025.


DOI:10.3389/fimmu.2025.1642091
PMID:40873588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12378638/
Abstract

Colon cancer persists as a major global health burden due to therapy resistance and metastasis, with tumor-associated macrophages (TAMs) in the microenvironment driving progression through immune evasion and angiogenesis. This review highlights plant-derived therapeutics targeting TAMs to disrupt protumor signaling. Key phytochemicals (e.g., Curcumin, Cucurbitacin B, Astragaloside IV) suppress M2 polarization via NF-κB/STAT3 inhibition, block VEGF/HIF-1α-mediated angiogenesis, and enhance antitumor immunity by downregulating PD-L1. Cannabidiol, Hydroxygenkwanin regulate TAM metabolism. Dietary agents like sulforaphane and β-glucans modulate TAM-gut microbiome crosstalk. Nanoparticle-encapsulated phytochemicals enhance TAM-targeted delivery, while clinical translation requires standardized phytopreparations and biomarker-guided trials. We propose integrating validated botanical adjuvants (e.g., Fucoidan for TLR4 inhibition, dihydroisotanshinone I for CCL2 suppression) with immunotherapies to remodel immunosuppressive niches. Phytotherapy offers a multifaceted strategy to overcome TAM-driven therapeutic barriers in colon cancer, emphasizing plant-based precision medicine to augment conventional treatments.

摘要

由于治疗耐药性和转移,结肠癌仍然是全球主要的健康负担,微环境中的肿瘤相关巨噬细胞(TAM)通过免疫逃避和血管生成推动疾病进展。本综述重点介绍了针对TAM以破坏促肿瘤信号传导的植物源疗法。关键植物化学物质(如姜黄素、葫芦素B、黄芪甲苷IV)通过抑制NF-κB/STAT3抑制M2极化,阻断VEGF/HIF-1α介导的血管生成,并通过下调PD-L1增强抗肿瘤免疫力。大麻二酚、羟基芫花素调节TAM代谢。萝卜硫素和β-葡聚糖等膳食剂可调节TAM与肠道微生物群的相互作用。纳米颗粒包裹的植物化学物质可增强TAM靶向递送,而临床转化需要标准化的植物制剂和生物标志物指导的试验。我们建议将经过验证的植物佐剂(如用于抑制TLR4的岩藻依聚糖、用于抑制CCL2的二氢异丹参酮I)与免疫疗法相结合,以重塑免疫抑制微环境。植物疗法提供了一种多方面的策略来克服TAM驱动的结肠癌治疗障碍,强调基于植物的精准医学以增强传统治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/15de683c85c5/fimmu-16-1642091-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/6d8952567059/fimmu-16-1642091-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/5bd42be9bf41/fimmu-16-1642091-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/559b5449a423/fimmu-16-1642091-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/15de683c85c5/fimmu-16-1642091-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/6d8952567059/fimmu-16-1642091-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/5bd42be9bf41/fimmu-16-1642091-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/559b5449a423/fimmu-16-1642091-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/190a/12378638/15de683c85c5/fimmu-16-1642091-g004.jpg

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Tumor-associated macrophages in colon cancer immunotherapy: mechanisms, natural product interventions, and microenvironment remodeling.

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本文引用的文献

[1]
VSIG4 Promotes Tumour-Associated Macrophage M2 Polarization and Immune Escape in Colorectal Cancer via Fatty Acid Oxidation Pathway.

Clin Transl Med. 2025-5

[2]
Chinese yam polysaccharide enhances anti-PD-1 immunotherapy in colorectal cancer through alterations in the gut microbiota and metabolites.

Int J Biol Macromol. 2025-5

[3]
Colon cancer exosome-associated HSP90B1 initiates pre-metastatic niche formation in the liver by polarizing M1 macrophage into M2 phenotype.

Biol Direct. 2025-4-15

[4]
Tetrahydrocurcumin alleviates colorectal tumorigenesis by modulating the SPP1/CD44 axis and preventing M2 tumor-associated macrophage polarization.

Phytomedicine. 2025-6

[5]
Targeted release of a bispecific fusion protein SIRPα/Siglec-10 by oncolytic adenovirus reinvigorates tumor-associated macrophages to improve therapeutic outcomes in solid tumors.

J Immunother Cancer. 2025-4-1

[6]
Tumor-Derived Exosomal circ_0020095 Promotes Colon Cancer Cell Proliferation and Metastasis by Inhibiting M1 Macrophage Polarization.

J Biochem Mol Toxicol. 2025-4

[7]
Exosomal miR-92a-3p modulates M2 macrophage polarization in colorectal cancer: implications for tumor migration and angiogenesis.

Med Oncol. 2025-3-10

[8]
Polarized Tissue-Derived Macrophages Display Enhanced M2d Phenotype after Prolonged Stimulation with Adenosine A Receptor Agonist in the Presence of LPS.

Front Biosci (Landmark Ed). 2025-2-17

[9]
Multifunctional nanodrug for simultaneously combating chemoresistance and immunosuppression in Fusobacterium nucleatum-associated colorectal cancer.

Acta Biomater. 2025-3-15

[10]
Targeting MAPK14 by Lobeline Upregulates Slurp1-Mediated Inhibition of Alternative Activation of TAM and Retards Colorectal Cancer Growth.

Adv Sci (Weinh). 2025-3

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