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肠道细菌与靶向治疗之间的相互作用:对未来癌症治疗的启示。

The interplay between gut bacteria and targeted therapies: implications for future cancer treatments.

作者信息

He Juan, Chen Yu, Zhao Huakan, Li Yongsheng

机构信息

Chongqing University Cancer Hospital, School of Medicine, Chongqing University, Chongqing, China.

Department of Medical Oncology, Chongqing University Cancer Hospital, 181 Hanyu Road, Shapingba District, Chongqing, 400030, China.

出版信息

Mol Med. 2025 Feb 13;31(1):58. doi: 10.1186/s10020-025-01108-6.

DOI:10.1186/s10020-025-01108-6
PMID:39948481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11827328/
Abstract

Targeted therapy represents a form of cancer treatment that specifically focuses on molecular markers regulating the growth, division, and dissemination of cancer cells. It serves as the cornerstone of precision medicine and is associated with fewer adverse effects compared to conventional chemotherapy, thus enhancing the quality of patient survival. These make targeted therapy as a vital component of contemporary anti-cancer strategies. Although targeted therapy has achieved excellent anti-cancer results, there are still many factors affecting its efficacy. Among the numerous factors affecting anti-cancer treatment, the role of intestinal bacteria and its metabolites are becoming increasingly prominent, particularly in immunotherapy. However, their effects on anticancer targeted therapy have not been systematically reviewed. Herein, we discuss the crosstalk between gut bacteria and anticancer targeted therapies, while also highlighting potential therapeutic strategies and future research directions.

摘要

靶向治疗是一种癌症治疗形式,它特别关注调节癌细胞生长、分裂和扩散的分子标志物。它是精准医学的基石,与传统化疗相比,副作用更少,从而提高了患者的生存质量。这些使得靶向治疗成为当代抗癌策略的重要组成部分。尽管靶向治疗已经取得了出色的抗癌效果,但仍有许多因素影响其疗效。在影响抗癌治疗的众多因素中,肠道细菌及其代谢产物的作用日益突出,尤其是在免疫治疗中。然而,它们对抗癌靶向治疗的影响尚未得到系统的综述。在此,我们讨论肠道细菌与抗癌靶向治疗之间的相互作用,同时强调潜在的治疗策略和未来的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/9df9f686d886/10020_2025_1108_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/52f81644275e/10020_2025_1108_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/1f2c27fbd1ae/10020_2025_1108_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/d37087afb43d/10020_2025_1108_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/9df9f686d886/10020_2025_1108_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/52f81644275e/10020_2025_1108_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/1f2c27fbd1ae/10020_2025_1108_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/d37087afb43d/10020_2025_1108_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92a/11827328/9df9f686d886/10020_2025_1108_Fig4_HTML.jpg

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本文引用的文献

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Nat Microbiol. 2024 Sep;9(9):2292-2307. doi: 10.1038/s41564-024-01784-w. Epub 2024 Aug 21.
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Therapeutic advances of targeting receptor tyrosine kinases in cancer.靶向治疗癌症受体酪氨酸激酶的治疗进展。
Signal Transduct Target Ther. 2024 Aug 14;9(1):201. doi: 10.1038/s41392-024-01899-w.
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Trimethylamine N-oxide promotes the proliferation and migration of hepatocellular carcinoma cell through the MAPK pathway.
氧化三甲胺通过丝裂原活化蛋白激酶(MAPK)途径促进肝癌细胞的增殖和迁移。
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Peptostreptococcus stomatis promotes colonic tumorigenesis and receptor tyrosine kinase inhibitor resistance by activating ERBB2-MAPK.口腔普氏菌通过激活 ERBB2-MAPK 促进结肠肿瘤发生和受体酪氨酸激酶抑制剂耐药。
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Black rice diet alleviates colorectal cancer development through modulating tryptophan metabolism and activating AHR pathway.黑米饮食通过调节色氨酸代谢和激活芳烃受体(AHR)途径减轻结直肠癌的发展。
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