Eubacterium coprostanoligenes alleviates chemotherapy-induced intestinal mucositis by enhancing intestinal mucus barrier

被引:15
作者
Bai, Dongsheng [1 ]
Zhao, Jiawei [1 ]
Wang, Runde [1 ]
Du, Jiaying [1 ]
Zhou, Chen [1 ]
Gu, Chunyang [1 ]
Wang, Yuxiang [1 ]
Zhang, Lulu [2 ]
Zhao, Yue [1 ]
Lu, Na [1 ]
机构
[1] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, State Key Lab Nat Med,Dept Physiol, Jiangsu Key Lab Carcinogenesis & Intervent, Nanjing 210009, Peoples R China
[2] Nanjing Med Univ, Sch Pharm, Dept Clin Pharmacol, Nanjing 211166, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemotherapy; Mucositis; Eubacterium coprostanoligenes; MUC2; AUF1; DISEASE SUSCEPTIBILITY; MUCIN; MICROBIOTA; EXPRESSION; 5-FLUOROURACIL; IRINOTECAN; TOXICITY; COLITIS; MODEL;
D O I
10.1016/j.apsb.2023.12.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemotherapy-induced mucositis represents a severe adverse outcome of cancer treatment, significantly curtailing the efficacy of these treatments and, in some cases, resulting in fatal consequences. Despite identifying intestinal epithelial cell damage as a key factor in chemotherapy-induced mucositis, the paucity of effective treatments for such damage is evident. In our study, we discovered that Eubacterium coprostanoligenes promotes mucin secretion by goblet cells, thereby fortifying the integrity of the intestinal mucus barrier. This enhanced barrier function serves to resist microbial invasion and subsequently reduces the inflammatory response. Importantly, this effect remains unobtrusive to the antitumor efficacy of chemotherapy drugs. Mechanistically, E. copr up-regulates the expression of AUF1, leading to the stabilization of Muc2 mRNA and an increase in mucin synthesis in goblet cells. An especially significant finding is that E. copr activates the AhR pathway, thereby promoting the expression of AUF1. In summary, our results strongly indicate that E. copr enhances the intestinal mucus barrier, effectively alleviating chemotherapy-induced intestinal mucositis by activating the AhR/AUF1 pathway, consequently enhancing Muc2 mRNA stability.
引用
收藏
页码:1677 / 1692
页数:16
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