普氏粪杆菌
代谢组
结直肠癌
小桶
肠道菌群
基因组
甘油磷脂
微生物群
生物
癌变
肥胖
拟杆菌
癌症
代谢组学
双歧杆菌
生物信息学
乳酸菌
遗传学
基因
转录组
免疫学
拟杆菌
细菌
内分泌学
磷脂
基因表达
膜
作者
Jinming Li,Ziying Chen,Qinying Wang,Lutao Du,Yongzhi Yang,Fanying Guo,Xinxiang Li,Yanjie Chao,Yanlei Ma
标识
DOI:10.1016/j.xcrm.2024.101429
摘要
Obesity is a risk factor for colorectal cancer (CRC), and the involvement of gut microbiota in the pathogenesis of obesity and CRC is widely recognized. However, the landscape of fecal microbiome and metabolome distinguishing patients with obesity-related CRC from obesity remains unknown. Here, we utilize metagenomic sequencing and metabolomics from 522 patients with CRC and healthy controls to identify the characteristics of obese CRC. Our integrated analysis reveals that obesity-related CRC is characterized by elevated Peptostreptococcus stomatis, dysregulated fatty acids and phospholipids, and altered Kyoto Encyclopedia of Genes and Genomes pathways involving glycerophospholipid metabolism and lipopolysaccharide synthesis. Correlation analysis unveils microbial interactions in obesity, where the probiotic Faecalibacterium prausnitzii and the tumor-promoting species P. stomatis may engage in cross-feeding, thereby promoting tumorigenesis. In vitro experiments affirm enhanced growth under cross-feeding conditions. The mutualistic microbe-microbe interaction may contribute to the association between obesity and elevated CRC risk. Additionally, diagnostic models incorporating BMI-specific microbial biomarkers display promise for precise CRC screening.
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