鹅去氧胆酸
癌症
结直肠癌
乳酸菌
内科学
胃肠病学
医学
内分泌学
生物
食品科学
胆汁酸
发酵
作者
Chen Liu,Peng Lai,Jiancong Hu,Shengmei Yin,Shuang Guo,Danling Liu,Jing Yu,Dayi Liang,Guangyuan Chen,Mengze Xing,Zhanhao Luo,Xiaosheng He,Junli Gong,Ping Lan,Zhen He
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2025-09-15
标识
DOI:10.1158/0008-5472.can-25-0879
摘要
High-fat diet (HFD) is positively correlated with colorectal cancer (CRC), but there are notable inter-individual differences in susceptibility to the tumor-promoting effects of HFD. A better understanding of the mechanisms that modulate the outcomes of HFD could help inform precision prevention strategies for CRC. Here, we found a key role for the gut microbiota in the individual differences observed in the tumor-promoting effects of HFD. Analysis of the gut bacteria enriched in mice resistant to HFD-induced cancer identified Lactobacillus johnsonii (L. johnsonii) as an effective protector. Colonization of L. johnsonii increased intestinal chenodeoxycholic acid (CDCA) concentrations in HFD-exposed mice, which decelerated HFD-induced CRC progression. Mechanistically, L. johnsonii converted conjugated bile acid to CDCA via bile salt hydrolase (BSH), and CDCA induced mitochondrial dysfunction and oxidative stress to promote apoptosis, effectively suppressing tumor development. These results establish the gut microbiota as a mediator of inter-individual differences in cancer susceptibility induced by HFD and reveal a probiotic strategy with the ability to inhibit tumorigenesis, suggesting a possible route to reduce HFD-induced CRC progression.
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