Association between Upper Digestive Tract Microbiota and Cancer-Predisposing States in the Esophagus and Stomach

被引:116
作者
Yu, Guoqin [1 ]
Gail, Mitchell H. [1 ]
Shi, Jianxin [1 ]
Klepac-Ceraj, Vanja [3 ,4 ]
Paster, Bruce J. [3 ,5 ]
Dye, Bruce A. [2 ]
Wang, Guo-Qing [6 ]
Wei, Wen-Qiang [6 ]
Fan, Jin-Hu [6 ]
Qiao, You-Lin [6 ]
Dawsey, Sanford M. [1 ]
Freedman, Neal D. [1 ]
Abnet, Christian C. [1 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
[2] Ctr Dis Control & Prevent, Natl Ctr Hlth Stat, Hyattsville, MD USA
[3] Forsyth Inst, Cambridge, MA USA
[4] Wellesley Coll, Wellesley, MA 02181 USA
[5] Harvard Univ, Sch Dent Med, Boston, MA 02115 USA
[6] Chinese Acad Med Sci, Inst Canc, Beijing 100021, Peoples R China
关键词
SQUAMOUS-CELL CARCINOMA; HELICOBACTER-PYLORI INFECTION; INFLAMMATORY BOWEL DISEASES; SERUM PEPSINOGENS; GUT MICROBIOME; GASTRIC-CANCER; PERNICIOUS-ANEMIA; HIGH-RISK; POPULATION; CHINA;
D O I
10.1158/1055-9965.EPI-13-0855
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The human upper digestive tract microbial community (microbiota) is not well characterized and few studies have explored how it relates to human health. We examined the relationship between upper digestive tract microbiota and two cancer-predisposing states, serum pepsinogen I/pepsinogen II ratio (PGI/II; predictor of gastric cancer risk) and esophageal squamous dysplasia (ESD; the precursor lesion of esophageal squamous cell carcinoma; ESCC) in a cross-sectional design. Methods: The Human Oral Microbe Identification Microarray was used to test for the presence of 272 bacterial species in 333 upper digestive tract samples from a Chinese cancer screening cohort. Serum PGI and PGII were determined by ELISA. ESD was determined by chromoendoscopy with biopsy. Results: Lower microbial richness (number of bacterial genera per sample) was significantly associated with lower PGI/II ratio (P = 0.034) and the presence of ESD (P = 0.018). We conducted principal component (PC) analysis on a beta-diversity matrix (pairwise difference in microbiota), and observed significant correlations between PC1, PC3, and PGI/II (P = 0.004 and 0.009, respectively), and between PC1 and ESD (P = 0.003). Conclusions: Lower microbial richness in upper digestive tract was independently associated with both cancer-predisposing states in the esophagus and stomach (presence of ESD and lower PGI/II). Impact: These novel findings suggest that the upper digestive tract microbiota may play a role in the etiology of chronic atrophic gastritis and ESD, and therefore in the development of gastric and esophageal cancers. (C) 2014 AACR.
引用
收藏
页码:735 / 741
页数:7
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