Nakatsu Geicho, Li Xiangchun, Zhou Haokui, Sheng Jianqiu, Wong Sunny Hei, Wu William Ka Kai, Ng Siew Chien, Tsoi Ho, Dong Yujuan, Zhang Ning, He Yuqi, Kang Qian, Cao Lei, Wang Kunning, Zhang Jingwan, Liang Qiaoyi, Yu Jun, Sung Joseph J Y
Department of Medicine and Therapeutics, Institute of Digestive Disease, State Key Laboratory of Digestive Disease, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, 30-32 Ngan Shing Street, Shatin, Hong Kong SAR, China.
CUHK Shenzhen Research Institute, 2 Yuexing Road, Nanshan District, Shenzhen 518057, China.
Nat Commun. 2015 Oct 30;6:8727. doi: 10.1038/ncomms9727.
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.
肠道微生物群落失调促进结直肠癌(CRC)的发生。在此,我们对结直肠癌发生不同阶段人类肠道黏膜中的微生物群落进行编目。我们分析了47对腺瘤与腺瘤相邻黏膜、52对癌与癌相邻黏膜的肠道黏膜微生物组以及61名健康对照。相对丰度谱的概率划分显示,以口腔微生物组成员为主的元群落主要与结直肠癌相关。配对样本分析显示病变部位与相邻黏膜之间的群落结构存在差异。细菌分类群的相关性表明腺瘤中存在失调的早期迹象,随后在癌症中共同排斥关系更为常见。通过与两个先前发表的数据集比较,我们验证了CRC相关微生物组中的这些改变。我们的结果表明,一个分类学定义的微生物群落与结直肠癌的发生有关。