Shifts in the Fecal Microbiota Associated with Adenomatous Polyps

被引:170
作者
Hale, Vanessa L. [1 ,2 ]
Chen, Jun [3 ]
Johnson, Stephen [3 ]
Harrington, Sean C. [2 ]
Yab, Tracy C. [4 ]
Smyrk, Thomas C. [5 ]
Nelson, Heidi [1 ]
Boardman, Lisa A. [4 ]
Druliner, Brooke R. [4 ]
Levin, Theodore R. [6 ]
Rex, Douglas K. [7 ]
Ahnen, Dennis J. [8 ]
Lance, Peter [9 ]
Ahlquist, David A. [4 ]
Chia, Nicholas [1 ,2 ,10 ,11 ]
机构
[1] Mayo Clin, Dept Surg, Rochester, MN USA
[2] Mayo Clin, Ctr Individualized Med, Microbiome Program, Rochester, MN USA
[3] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[4] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[5] Mayo Clin, Div Anat Patol, Rochester, MN USA
[6] Kaiser Permanente, Div Gastroenterol, Oakland, CA USA
[7] Indiana Univ Sch Med, Div Gastroenterol, Indianapolis, IN 46202 USA
[8] Univ Colorado, Sch Med, Denver Dept Vetarans Affairs, Med Ctr, Denver, CO USA
[9] Univ Arizona, Ctr Canc, Tucson, AZ USA
[10] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA
[11] Mayo Clin, Dept Physiol & Biomed Engn, Rochester, MN USA
关键词
16S RIBOSOMAL-RNA; COLORECTAL-CANCER; GUT MICROBIOME; BILE-ACIDS; MOGIBACTERIUM-TIMIDUM; DIETARY PATTERNS; RISK; METABOLITES; PREVENTION; DYSBIOSIS;
D O I
10.1158/1055-9965.EPI-16-0337
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Adenomatous polyps are the most common precursor to colorectal cancer, the second leading cause of cancer-related death in the United States. We sought to learn more about early events of carcinogenesis by investigating shifts in the gut microbiota of patients with adenomas. Methods: We analyzed 16S rRNA gene sequences from the fecal microbiota of patients with adenomas (n = 233) and without (n = 547). Results: Multiple taxa were significantly more abundant in patients with adenomas, including Bilophila, Desulfovibrio, proinflammatory bacteria in the genus Mogibacterium, and multiple Bacteroidetes species. Patients without adenomas had greater abundances of Veillonella, Firmicutes (Order Clostridia), and Actinobacteria (family Bifidobacteriales). Our findings were consistent with previously reported shifts in the gut microbiota of colorectal cancer patients. Importantly, the altered adenoma profile is predicted to increase primary and secondary bile acid production, as well as starch, sucrose, lipid, and phenylpropanoid metabolism. Conclusions: These data hint that increased sugar, protein, and lipid metabolism along with increased bile acid production could promote a colonic environment that supports the growth of bile-tolerant microbes such as Bilophilia and Desulfovibrio. In turn, these microbes may produce genotoxic or inflammatory metabolites such as H2S and secondary bile acids, which could play a role in catalyzing adenoma development and eventually colorectal cancer. Impact: This study suggests a plausible biological mechanism to explain the links between shifts in the microbiota and colorectal cancer. This represents a first step toward resolving the complex interactions that shape the adenoma-carcinoma sequence of colorectal cancer and may facilitate personalized therapeutics focused on the microbiota. (C)2016 AACR.
引用
收藏
页码:85 / 94
页数:10
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