Recent metagenomic studies have discovered gut microbiome signatures in colonic tissues from patients with colorectal cancer or adenomas, suggesting a potential causal link between gut microbiome and the development of colorectal neoplasia. Diet clearly plays an important etiological role in colon carcinogenesis. It is long believed that diet is a major determinant of the human gut microbiota composition. Three recent landmark studies have provided compelling evidence supporting this notion, each having found similar microbiome core signatures. Furthermore, human gut microbiome signature or ?enterotype? is strongly associated with an individual?s long-term diet pattern, but not with short-term dietary changes. To date, few studies have comprehensively examined the complex interplay of fecal microbiome, diet, and risk of colon adenoma. Therefore, we propose a metagenomic molecular epidemiology study to address our hypothesis that diet-associated gut microbiome signatures are associated with risk of colon adenoma. This proposal builds upon a relatively large cohort of patients undergoing screening colonoscopy who are being recruited into the parent GI SPORE project for a stool- based methylation biomarker study for early detection of colon adenomas.
We aim to: 1) indentify gut microbiome signatures associated with habitual diet; 2) examine the association of gut microbiome signatures with risk of colon adenoma; and 3) assess direct and gut microbiome-mediated effects of diet on risk of colon adenoma.
These aims will be accomplished by using the existing Cleveland Risk Factors and Early Detection of Colon Adenoma cohort population, where rich dietary and epidemiological data and pre-screening stool samples are being collected from 1,600 average-risk patients as part of parent Case GI SPORE program.

Public Health Relevance

This project uses state-of-art deep sequencing technology and bioinformatics methodology to study human gut microbiome, and its interplay with diet in relation to risk of colon adenoma. This study will generate novel knowledge of the etiological role of gut microbiome in colon carcinogenesis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
1R03CA212558-01
Application #
9231051
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Lam, Tram K
Project Start
2017-01-01
Project End
2018-12-31
Budget Start
2017-01-01
Budget End
2017-12-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Family Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106