Gut mucosal microbiome across stages of colorectal carcinogenesis

Geicho Nakatsu(Chinese University of Hong Kong), Xiangchun Li(Chinese University of Hong Kong), Haokui Zhou(Chinese University of Hong Kong), Jian-qiu Sheng(The Military General Hospital of Beijing PLA), Sunny H. Wong(Chinese University of Hong Kong), William Ka Kei Wu(Chinese University of Hong Kong), Siew C. Ng(Chinese University of Hong Kong), Ho Tsoi(Chinese University of Hong Kong), Yujuan Dong(Chinese University of Hong Kong), Ning Zhang(Sun Yat-sen University), Yuqi He(The Military General Hospital of Beijing PLA), Qian Kang(The Military General Hospital of Beijing PLA), Lei Cao(Chinese University of Hong Kong), Kunning Wang(Chinese University of Hong Kong), Jingwan Zhang(Chinese University of Hong Kong), Qiaoyi Liang(Chinese University of Hong Kong), Jun Yu(Chinese University of Hong Kong), Joseph J.�Y. Sung(Chinese University of Hong Kong)
Nature Communications
October 30, 2015
Cited by 702Open Access
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Abstract

Gut microbial dysbiosis contributes to the development of colorectal cancer (CRC). Here we catalogue the microbial communities in human gut mucosae at different stages of colorectal tumorigenesis. We analyse the gut mucosal microbiome of 47 paired samples of adenoma and adenoma-adjacent mucosae, 52 paired samples of carcinoma and carcinoma-adjacent mucosae and 61 healthy controls. Probabilistic partitioning of relative abundance profiles reveals that a metacommunity predominated by members of the oral microbiome is primarily associated with CRC. Analysis of paired samples shows differences in community configurations between lesions and the adjacent mucosae. Correlations of bacterial taxa indicate early signs of dysbiosis in adenoma, and co-exclusive relationships are subsequently more common in cancer. We validate these alterations in CRC-associated microbiome by comparison with two previously published data sets. Our results suggest that a taxonomically defined microbial consortium is implicated in the development of CRC.


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