• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向饮食和微生物色氨酸-吲哚代谢作为结肠癌的治疗方法。

Targeting Dietary and Microbial Tryptophan-Indole Metabolism as Therapeutic Approaches to Colon Cancer.

机构信息

Human Health, Performance and Recreation, Robbins College of Health and Human Sciences, Baylor University, Waco, TX 76798-7346, USA.

Human Science and Design, Robbins College of Health and Human Sciences, Baylor University, Waco, TX 76798-7346, USA.

出版信息

Nutrients. 2021 Apr 3;13(4):1189. doi: 10.3390/nu13041189.

DOI:10.3390/nu13041189
PMID:33916690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8066279/
Abstract

Tryptophan metabolism, via the kynurenine (Kyn) pathway, and microbial transformation of tryptophan to indolic compounds are fundamental for host health; both of which are altered in colon carcinogenesis. Alterations in tryptophan metabolism begin early in colon carcinogenesis as an adaptive mechanism for the tumor to escape immune surveillance and metastasize. The microbial community is a key part of the tumor microenvironment and influences cancer initiation, promotion and treatment response. A growing awareness of the impact of the microbiome on tryptophan (Trp) metabolism in the context of carcinogenesis has prompted this review. We first compare the different metabolic pathways of Trp under normal cellular physiology to colon carcinogenesis, in both the host cells and the microbiome. Second, we review how the microbiome, specifically indoles, influence host tryptophan pathways under normal and oncogenic metabolism. We conclude by proposing several dietary, microbial and drug therapeutic modalities that can be utilized in combination to abrogate tumorigenesis.

摘要

色氨酸代谢途径(通过犬尿氨酸途径)和色氨酸转化为吲哚化合物的微生物转化对于宿主健康至关重要,而这两者在结肠癌变中都会发生改变。在结肠癌变的早期,色氨酸代谢的改变是肿瘤为逃避免疫监视和转移而产生的一种适应性机制。微生物群落是肿瘤微环境的关键组成部分,影响癌症的发生、促进和治疗反应。人们越来越意识到微生物组对致癌作用下色氨酸(Trp)代谢的影响,这促使我们进行了本次综述。我们首先比较了正常细胞生理条件下和结肠癌变过程中宿主细胞和微生物组中色氨酸代谢的不同途径。其次,我们综述了微生物组,特别是吲哚,如何在正常和致癌代谢下影响宿主色氨酸途径。最后,我们提出了几种可以联合使用的饮食、微生物和药物治疗方式来消除肿瘤发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/ccf3b655aa7a/nutrients-13-01189-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/448416bc88a9/nutrients-13-01189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/30d8dfecab3e/nutrients-13-01189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/ccf3b655aa7a/nutrients-13-01189-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/448416bc88a9/nutrients-13-01189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/30d8dfecab3e/nutrients-13-01189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d973/8066279/ccf3b655aa7a/nutrients-13-01189-g003.jpg

相似文献

1
Targeting Dietary and Microbial Tryptophan-Indole Metabolism as Therapeutic Approaches to Colon Cancer.靶向饮食和微生物色氨酸-吲哚代谢作为结肠癌的治疗方法。
Nutrients. 2021 Apr 3;13(4):1189. doi: 10.3390/nu13041189.
2
Oral tryptophan activates duodenal aryl hydrocarbon receptor in healthy subjects: a crossover randomized controlled trial.口服色氨酸激活健康受试者十二指肠芳烃受体:一项交叉随机对照试验。
Am J Physiol Gastrointest Liver Physiol. 2024 Jun 1;326(6):G687-G696. doi: 10.1152/ajpgi.00306.2023. Epub 2024 Apr 9.
3
Amino Acid Trp: The Far Out Impacts of Host and Commensal Tryptophan Metabolism.氨基酸色氨酸:宿主和共生色氨酸代谢的深远影响。
Front Immunol. 2021 Jun 4;12:653208. doi: 10.3389/fimmu.2021.653208. eCollection 2021.
4
Reimagining IDO Pathway Inhibition in Cancer Immunotherapy via Downstream Focus on the Tryptophan-Kynurenine-Aryl Hydrocarbon Axis.通过下游聚焦色氨酸-犬尿氨酸-芳烃轴重新构想癌症免疫治疗中的 IDO 途径抑制。
Clin Cancer Res. 2019 Mar 1;25(5):1462-1471. doi: 10.1158/1078-0432.CCR-18-2882. Epub 2018 Oct 30.
5
Tryptophan metabolism induced by TDO2 promotes prostatic cancer chemotherapy resistance in a AhR/c-Myc dependent manner.TDO2 诱导的色氨酸代谢通过 AhR/c-Myc 依赖性途径促进前列腺癌化疗耐药。
BMC Cancer. 2021 Oct 17;21(1):1112. doi: 10.1186/s12885-021-08855-9.
6
Associations of microbial and indoleamine-2,3-dioxygenase-derived tryptophan metabolites with immune activation in healthy adults.健康成年人中微生物和色氨酸 2,3-双加氧酶衍生色氨酸代谢物与免疫激活的关联。
Front Immunol. 2022 Sep 29;13:917966. doi: 10.3389/fimmu.2022.917966. eCollection 2022.
7
Evading immunity: new enzyme implicated in cancer.逃避免疫:与癌症相关的新酶
J Natl Cancer Inst. 2012 Mar 7;104(5):349-52. doi: 10.1093/jnci/djs152. Epub 2012 Feb 20.
8
Targeting Tryptophan Catabolism in Cancer Immunotherapy Era: Challenges and Perspectives.在癌症免疫治疗时代靶向色氨酸代谢:挑战与展望。
Front Immunol. 2022 Jan 31;13:807271. doi: 10.3389/fimmu.2022.807271. eCollection 2022.
9
Involvement of the microbiota-gut-brain axis in chronic restraint stress: disturbances of the kynurenine metabolic pathway in both the gut and brain.肠道菌群-肠-脑轴在慢性束缚应激中的作用:肠道和大脑中犬尿氨酸代谢途径的紊乱。
Gut Microbes. 2021 Jan-Dec;13(1):1-16. doi: 10.1080/19490976.2020.1869501.
10
Kynurenine produced by indoleamine 2,3-dioxygenase 2 exacerbates acute liver injury by carbon tetrachloride in mice.吲哚胺 2,3-双加氧酶 2 产生的犬尿氨酸通过加剧四氯化碳诱导的小鼠急性肝损伤。
Toxicology. 2020 May 30;438:152458. doi: 10.1016/j.tox.2020.152458. Epub 2020 Apr 11.

引用本文的文献

1
Metabolic interactions: how gut microbial metabolites influence colorectal cancer.代谢相互作用:肠道微生物代谢产物如何影响结直肠癌
Front Microbiol. 2025 Jul 23;16:1611698. doi: 10.3389/fmicb.2025.1611698. eCollection 2025.
2
Gut microbiota shapes cancer immunotherapy responses.肠道微生物群塑造癌症免疫治疗反应。
NPJ Biofilms Microbiomes. 2025 Jul 25;11(1):143. doi: 10.1038/s41522-025-00786-8.
3
Oral oncolytic magnetotactic bacteria elicit anti-colorectal tumor immunity and reprogram microbiota metabolism.口服溶瘤趋磁细菌可引发抗结直肠癌免疫并重塑微生物群代谢。

本文引用的文献

1
Targeting regulation of tryptophan metabolism for colorectal cancer therapy: a systematic review.靶向色氨酸代谢调控用于结直肠癌治疗:一项系统综述
RSC Adv. 2019 Jan 23;9(6):3072-3080. doi: 10.1039/c8ra08520j. eCollection 2019 Jan 22.
2
Alteration of fecal tryptophan metabolism correlates with shifted microbiota and may be involved in pathogenesis of colorectal cancer.粪便色氨酸代谢的改变与菌群移位相关,并可能与结直肠癌的发病机制有关。
World J Gastroenterol. 2020 Dec 7;26(45):7173-7190. doi: 10.3748/wjg.v26.i45.7173.
3
Indole Propionic Acid, an Unusual Antibiotic Produced by the Gut Microbiota, With Anti-inflammatory and Antioxidant Properties.
Bioact Mater. 2025 Jun 29;51:909-923. doi: 10.1016/j.bioactmat.2025.06.046. eCollection 2025 Sep.
4
Global research trends in tryptophan metabolism and cancer: a bibliometric and visualization analysis (2005-2024).色氨酸代谢与癌症的全球研究趋势:文献计量与可视化分析(2005 - 2024年)
Front Oncol. 2025 Jul 1;15:1621666. doi: 10.3389/fonc.2025.1621666. eCollection 2025.
5
Dietary Manipulation on Gut Microbiome in Patients with Diabetes and Colorectal cancer.糖尿病和结直肠癌患者肠道微生物群的饮食调控
Curr Nutr Rep. 2025 Jun 3;14(1):75. doi: 10.1007/s13668-025-00667-8.
6
The Kynurenine Pathway and Indole Pathway in Tryptophan Metabolism Influence Tumor Progression.色氨酸代谢中的犬尿氨酸途径和吲哚途径影响肿瘤进展。
Cancer Med. 2025 Mar;14(6):e70703. doi: 10.1002/cam4.70703.
7
Targeting the Kynurenine Pathway: A Novel Approach in Tumor Therapy.靶向犬尿氨酸途径:肿瘤治疗的新方法。
Expert Rev Mol Med. 2025 Mar 5;27:1-33. doi: 10.1017/erm.2025.5.
8
The Role of Indoxyl Sulfate in Exacerbating Colorectal Cancer During Chronic Kidney Disease Progression: Insights into the Akt/β-Catenin/c-Myc and AhR/c-Myc Pathways in HCT-116 Colorectal Cancer Cells.硫酸吲哚酚在慢性肾脏病进展过程中加重结直肠癌的作用:对HCT-116结肠癌细胞中Akt/β-连环蛋白/c-Myc和芳烃受体/c-Myc信号通路的见解
Toxins (Basel). 2025 Jan 1;17(1):17. doi: 10.3390/toxins17010017.
9
Exploring the biological impact of bacteria-derived indole compounds on human cell health: Cytotoxicity and cell proliferation across six cell lines.探索细菌衍生的吲哚化合物对人类细胞健康的生物学影响:六种细胞系的细胞毒性和细胞增殖
Toxicol Rep. 2024 Dec 24;14:101883. doi: 10.1016/j.toxrep.2024.101883. eCollection 2025 Jun.
10
Higher physical activity levels are related to faecal microbiota diversity and composition in young adults.较高的身体活动水平与年轻人的粪便微生物群多样性和组成有关。
Biol Sport. 2025 Jan;42(1):123-135. doi: 10.5114/biolsport.2025.139850. Epub 2024 Jun 4.
吲哚丙酸,一种由肠道微生物群产生的特殊抗生素,具有抗炎和抗氧化特性。
Front Microbiol. 2020 Oct 27;11:575586. doi: 10.3389/fmicb.2020.575586. eCollection 2020.
4
Metabolites of microbiota response to tryptophan and intestinal mucosal immunity: A therapeutic target to control intestinal inflammation.肠道微生物群响应色氨酸和肠黏膜免疫的代谢产物:控制肠道炎症的治疗靶点。
Med Res Rev. 2021 Mar;41(2):1061-1088. doi: 10.1002/med.21752. Epub 2020 Nov 10.
5
Drug Mimicry: Promiscuous Receptors PXR and AhR, and Microbial Metabolite Interactions in the Intestine.药物模拟:多态性受体 PXR 和 AhR 以及肠道中的微生物代谢物相互作用。
Trends Pharmacol Sci. 2020 Dec;41(12):900-908. doi: 10.1016/j.tips.2020.09.013. Epub 2020 Oct 20.
6
Serum kynurenine levels are a novel biomarker to predict the prognosis of patients with hepatocellular carcinoma.血清犬尿氨酸水平是预测肝细胞癌患者预后的新型生物标志物。
PLoS One. 2020 Oct 21;15(10):e0241002. doi: 10.1371/journal.pone.0241002. eCollection 2020.
7
IDO Expression in Cancer: Different Compartment, Different Functionality?IDO 在癌症中的表达:不同部位,不同功能?
Front Immunol. 2020 Sep 24;11:531491. doi: 10.3389/fimmu.2020.531491. eCollection 2020.
8
Polyamines and Kynurenines at the Intersection of Immune Modulation.多胺与犬尿氨酸在免疫调节中的交汇点
Trends Immunol. 2020 Nov;41(11):1037-1050. doi: 10.1016/j.it.2020.09.007. Epub 2020 Oct 12.
9
FadA promotes DNA damage and progression of Fusobacterium nucleatum-induced colorectal cancer through up-regulation of chk2.FadA 通过上调 chk2 促进具核梭杆菌诱导的结直肠癌的 DNA 损伤和进展。
J Exp Clin Cancer Res. 2020 Sep 29;39(1):202. doi: 10.1186/s13046-020-01677-w.
10
Nutritional Therapy to Modulate Tryptophan Metabolism and Aryl Hydrocarbon-Receptor Signaling Activation in Human Diseases.营养疗法调节色氨酸代谢和芳香烃受体信号激活在人类疾病中的作用。
Nutrients. 2020 Sep 17;12(9):2846. doi: 10.3390/nu12092846.