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饮食与肠道微生物群在癌症中的相互作用。

Interactions between diet and gut microbiota in cancer.

机构信息

Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Harvard Chan Microbiome in Public Health Center, Boston, MA, USA.

出版信息

Nat Microbiol. 2024 Jul;9(7):1644-1654. doi: 10.1038/s41564-024-01736-4. Epub 2024 Jun 21.

DOI:10.1038/s41564-024-01736-4
PMID:38907007
Abstract

Dietary patterns and specific dietary components, in concert with the gut microbiota, can jointly shape susceptibility, resistance and therapeutic response to cancer. Which diet-microbial interactions contribute to or mitigate carcinogenesis and how they work are important questions in this growing field. Here we interpret studies of diet-microbial interactions to assess dietary determinants of intestinal colonization by opportunistic and oncogenic bacteria. We explore how diet-induced expansion of specific gut bacteria might drive colonic epithelial tumorigenesis or create immuno-permissive tumour milieus and introduce recent findings that provide insight into these processes. Additionally, we describe available preclinical models that are widely used to study diet, microbiome and cancer interactions. Given the rising clinical interest in dietary modulations in cancer treatment, we highlight promising clinical trials that describe the effects of different dietary alterations on the microbiome and cancer outcomes.

摘要

饮食模式和特定的饮食成分,与肠道微生物群一起,可以共同塑造对癌症的易感性、抵抗力和治疗反应。哪些饮食-微生物相互作用有助于或减轻致癌作用,以及它们是如何工作的,这是这个不断发展的领域的重要问题。在这里,我们解释饮食-微生物相互作用的研究,以评估饮食对机会性和致癌细菌肠道定植的决定因素。我们探讨了饮食诱导的特定肠道细菌的扩张如何驱动结肠上皮肿瘤发生,或创造免疫允许的肿瘤微环境,并介绍了最近的发现,这些发现为了解这些过程提供了线索。此外,我们还描述了广泛用于研究饮食、微生物组和癌症相互作用的现有临床前模型。鉴于临床对癌症治疗中饮食调节的兴趣日益增加,我们重点介绍了一些有前途的临床试验,这些试验描述了不同饮食改变对微生物组和癌症结果的影响。

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本文引用的文献

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Nat Microbiol. 2024 Apr;9(4):922-937. doi: 10.1038/s41564-024-01628-7. Epub 2024 Mar 19.
2
Nutrition and dietary restrictions in cancer prevention.癌症预防中的营养与饮食限制。
Biochim Biophys Acta Rev Cancer. 2024 Jan;1879(1):189063. doi: 10.1016/j.bbcan.2023.189063. Epub 2023 Dec 24.
3
Methionine restriction-induced sulfur deficiency impairs antitumour immunity partially through gut microbiota.
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Arch Public Health. 2025 Aug 11;83(1):209. doi: 10.1186/s13690-025-01685-2.
4
Metabolic Adaptations in Cancer Progression: Optimization Strategies and Therapeutic Targets.癌症进展中的代谢适应:优化策略与治疗靶点
Cancers (Basel). 2025 Jul 15;17(14):2341. doi: 10.3390/cancers17142341.
5
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。
Bioact Mater. 2025 Jun 29;51:909-923. doi: 10.1016/j.bioactmat.2025.06.046. eCollection 2025 Sep.
6
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