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健脾解毒汤通过色氨酸代谢-AhR 途径抑制 TAMs 的 M2 极化来抑制结直肠癌细胞生长。

Jianpi Jiedu decoction suppresses colorectal cancer growth by inhibiting M2 polarization of TAMs through the tryptophan metabolism-AhR pathway.

机构信息

Department of Integrated Traditional Chinese & Western Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China; National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, 410011, China.

Department of Addiction Medicine, Hunan Institute of Mental Health, Brain Hospital of Hunan Province (The Second People's Hospital of Hunan Province), Changsha, Hunan, 410007, China.

出版信息

Int Immunopharmacol. 2024 Sep 10;138:112610. doi: 10.1016/j.intimp.2024.112610. Epub 2024 Jul 3.


DOI:10.1016/j.intimp.2024.112610
PMID:38963982
Abstract

BACKGROUND: Traditional Chinese medicine, JianpiJiedu decoction (JPJDF), has been utilized in colorectal cancer (CRC) treatment for over forty years. The potential of JPJDF to inhibit CRC through modulation of intestinal microbiota and their metabolites remains uncertain. AIMS: This study aims to further investigate the therapeutic mechanisms of JPJDF in CRC. METHODS: CAC mouse models were developed using azoxymethane (AOM) and dextran sulfate sodium (DSS). Intestinal tissues and contents underwent 16S rRNA gene sequencing and untargeted metabolomics analysis. Serum levels of IL-1β and TNF-α were measured using ELISA. Immunohistochemistry was utilized to assess the expression of Ki67, ZO-1, Occludin, CD68, and CD206. Furthermore, western blotting was performed to evaluate the protein expression of AhR and NF-κB. RESULTS: JPJDF inhibited colorectal tumourigenesis in AOM/DSS treated mice, while also suppressing tumor cell proliferation and upregulating the expression of tight junction proteins. The results of 16S rRNA gene sequencing analysis revealed that JPJDF altered intestinal microbiota composition by increasing the abundance of beneficial bacteria. Additionally, JPJDF reduced tryptophan metabolites, effectively alleviating inflammation and significantly restoring intestinal barrier function in CAC mice. Molecular biology experiments confirmed that JPJDF suppressed the expression levels of AhR and M2-type tumor-associated macrophages, thereby promoting anti-tumor immunity and exerting inhibitory effects on CAC growth. CONCLUSION: JPJDF can regulate the tryptophan metabolism-AhR pathway by modulating the gut microbiota, reducing intestinal inflammation, improving intestinal barrier function, enhancing anti-tumor immunity, and effectively inhibiting CAC growth.

摘要

背景:传统中药健脾解毒汤(JPJDF)已用于结直肠癌(CRC)治疗四十余年。JPJDF 通过调节肠道微生物群及其代谢物来抑制 CRC 的潜力尚不确定。

目的:本研究旨在进一步探讨 JPJDF 在 CRC 中的治疗机制。

方法:采用氧化偶氮甲烷(AOM)和葡聚糖硫酸钠(DSS)建立 CAC 小鼠模型。对肠道组织和内容物进行 16S rRNA 基因测序和非靶向代谢组学分析。采用 ELISA 法检测血清中 IL-1β和 TNF-α的水平。采用免疫组织化学法检测 Ki67、ZO-1、Occludin、CD68 和 CD206 的表达。此外,采用 Western blot 法评估 AhR 和 NF-κB 的蛋白表达。

结果:JPJDF 抑制了 AOM/DSS 处理的小鼠结直肠肿瘤的发生,同时抑制肿瘤细胞增殖并上调紧密连接蛋白的表达。16S rRNA 基因测序分析结果表明,JPJDF 通过增加有益菌的丰度改变了肠道微生物群落组成。此外,JPJDF 减少了色氨酸代谢物,有效缓解了炎症,并显著恢复了 CAC 小鼠的肠道屏障功能。分子生物学实验证实,JPJDF 抑制了 AhR 和 M2 型肿瘤相关巨噬细胞的表达水平,从而促进了抗肿瘤免疫,并对 CAC 的生长发挥了抑制作用。

结论:JPJDF 可通过调节肠道微生物群、减轻肠道炎症、改善肠道屏障功能、增强抗肿瘤免疫来调节色氨酸代谢-AhR 通路,有效抑制 CAC 的生长。

相似文献

[1]
Jianpi Jiedu decoction suppresses colorectal cancer growth by inhibiting M2 polarization of TAMs through the tryptophan metabolism-AhR pathway.

Int Immunopharmacol. 2024-9-10

[2]
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J Ethnopharmacol. 2023-2-10

[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
Integration of microbiome, metabolomics and transcriptome for in-depth understanding of berberine attenuates AOM/DSS-induced colitis-associated colorectal cancer.

Biomed Pharmacother. 2024-10

引用本文的文献

[1]
Metabolic reprogramming and immunosenescence in colorectal cancer: mechanisms and therapeutic implications.

Front Cell Dev Biol. 2025-8-13

[2]
Parabacteroides johnsonii inhibits the onset and progression of colorectal cancer by modulating the gut microbiota.

J Transl Med. 2025-7-2

[3]
Immunometabolism of Innate Immune Cells in Gastrointestinal Cancer.

Cancers (Basel). 2025-4-27

[4]
Influence of gut microbial metabolites on tumor immunotherapy: mechanisms and potential natural products.

Front Immunol. 2025-2-24

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