Gut microbiota interactions with antitumor immunity in colorectal cancer: From understanding to application

被引:19
作者
Zhuang, Yu-Pei [1 ,2 ]
Zhou, Hong-Li [3 ]
Chen, Hai-Bin [1 ]
Zheng, Ming-Yue [1 ,2 ]
Liang, Yu-Wei [1 ,2 ]
Gu, Yu-Tian [1 ,2 ]
Li, Wen-Ting [1 ,2 ]
Qiu, Wen -Li [1 ,4 ]
Zhou, Hong-Guang [1 ,2 ]
机构
[1] Nanjing Univ Chinese Med, Affiliated Hosp, Dept Oncol, Nanjing, Peoples R China
[2] Nanjing Univ Chinese Med, Clin Coll 1, Jiangsu Collaborat Innovat Ctr Tradit Chinese Med, Nanjing, Peoples R China
[3] Nanjing Univ Chinese Med, Coll Pharm, Nanjing, Peoples R China
[4] Nanjing Univ Chinese Med, Affiliated Hosp, Dept Radiol, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal cancer; Gut microbiota; Tumor immunity; Modulation strategies; MUCOSA-ASSOCIATED MICROBIOTA; FUSOBACTERIUM-NUCLEATUM; INTESTINAL MICROBIOTA; COLON-CANCER; TUMOR MICROENVIRONMENT; CHECKPOINT INHIBITORS; OVERCOMES RESISTANCE; THERAPY EFFICACY; DIETARY FIBER; PHAGE THERAPY;
D O I
10.1016/j.biopha.2023.115040
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Colorectal cancer (CRC) is one of highly prevalent cancer. Immunotherapy with immune checkpoint inhibitors (ICIs) has dramatically changed the landscape of treatment for many advanced cancers, but CRC still exhibits suboptimal response to immunotherapy. The gut microbiota can affect both anti-tumor and pro-tumor immune responses, and further modulate the efficacy of cancer immunotherapy, particularly in the context of therapy with ICIs. Therefore, a deeper understanding of how the gut microbiota modulates immune responses is crucial to improve the outcomes of CRC patients receiving immunotherapy and to overcome resistance in nonresponders. The present review aims to describe the relationship between the gut microbiota, CRC, and antitumor immune responses, with a particular focus on key studies and recent findings on the effect of the gut microbiota on the antitumor immune activity. We also discuss the potential mechanisms by which the gut microbiota influences host antitumor immune responses as well as the prospective role of intestinal flora in CRC treatment. Further-more, the therapeutic potential and limitations of different modulation strategies for the gut microbiota are also discussed. These insights may facilitate to better comprehend the interplay between the gut microbiota and the antitumor immune responses of CRC patients and provide new research pathways to enhance immunotherapy efficacy and expand the patient population that could be benefited by immunotherapy.
引用
收藏
页数:24
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