The multispecies microbial cluster of Fusobacterium, Parvimonas, Bacteroides and Faecalibacterium as a precision biomarker for colorectal cancer diagnosis

梭杆菌 生物标志物 普氏粪杆菌 结直肠癌 脆弱类杆菌 消化链球菌 拟杆菌 微生物学 普雷沃菌属 生物 肠道菌群 拟杆菌科 核梭杆菌 医学 胃肠病学 癌症 内科学 牙周炎 免疫学 细菌 粪便 遗传学 抗生素 牙龈卟啉单胞菌 生物化学
作者
Kelly Conde‐Pérez,Pablo Aja‐Macaya,Elena Buetas,Noelia Trigo‐Tasende,Mohammed Nasser‐Ali,Soraya Rumbo‐Feal,Paula Nión,Elsa Martín‐De Arribas,Lara S. Estévez,Begoña Otero‐Alén,José F. Noguera,Ángel Concha,Simón Pardiñas‐López,Miguel Carda‐Diéguez,M.I. Gomez-Randulfe Rodriguez,Nieves Martínez Lago,Susana Ladra,Luis M. A. Aparicio,Germán Bou,Álex Mira,Juán A. Vallejo,Margarita Poza
出处
期刊:Molecular Oncology [Wiley]
卷期号:18 (5): 1093-1122 被引量:3
标识
DOI:10.1002/1878-0261.13604
摘要

The incidence of colorectal cancer (CRC) has increased worldwide, and early diagnosis is crucial to reduce mortality rates. Therefore, new noninvasive biomarkers for CRC are required. Recent studies have revealed an imbalance in the oral and gut microbiomes of patients with CRC, as well as impaired gut vascular barrier function. In the present study, the microbiomes of saliva, crevicular fluid, feces, and non‐neoplastic and tumor intestinal tissue samples of 93 CRC patients and 30 healthy individuals without digestive disorders (non‐CRC) were analyzed by 16S rRNA metabarcoding procedures. The data revealed that Parvimonas , Fusobacterium , and Bacteroides fragilis were significantly over‐represented in stool samples of CRC patients, whereas Faecalibacterium and Blautia were significantly over‐abundant in the non‐CRC group. Moreover, the tumor samples were enriched in well‐known periodontal anaerobes, including Fusobacterium , Parvimonas , Peptostreptococcus , Porphyromonas , and Prevotella . Co‐occurrence patterns of these oral microorganisms were observed in the subgingival pocket and in the tumor tissues of CRC patients, where they also correlated with other gut microbes, such as Hungatella . This study provides new evidence that oral pathobionts, normally located in subgingival pockets, can migrate to the colon and probably aggregate with aerobic bacteria, forming synergistic consortia. Furthermore, we suggest that the group composed of Fusobacterium , Parvimonas , Bacteroides , and Faecalibacterium could be used to design an excellent noninvasive fecal test for the early diagnosis of CRC. The combination of these four genera would significantly improve the reliability of a discriminatory test with respect to others that use a single species as a unique CRC biomarker.
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