首页 | 本学科首页   官方微博 | 高级检索  
     


The gut microbiota associated with high-Gleason prostate cancer
Authors:Makoto Matsushita  Kazutoshi Fujita  Daisuke Motooka  Koji Hatano  Shota Fukae  Norihiko Kawamura  Eisuke Tomiyama  Yujiro Hayashi  Eri Banno  Tetsuya Takao  Shingo Takada  Shinichi Yachida  Hirotsugu Uemura  Shota Nakamura  Norio Nonomura
Affiliation:1. Department of Urology, Graduate School of Medicine, Osaka University, Suita, Japan;2. Department of Infection Metagenomics, Research Institute for Microbial Diseases, Osaka University, Suita, Japan;3. Department of Urology, Osaka Police Hospital, Osaka, Japan;4. Department of Urology, Osaka General Medical Center, Osaka, Japan;5. Department of Urology, Faculty of Medicine, Kindai University, Osakasayama, Japan;6. Department of Cancer Genome Informatics, Graduate School of Medicine, Osaka University, Suita, Japan
Abstract:We have found that intestinal bacteria and their metabolites, short-chain fatty acids (SCFAs), promote cancer growth in prostate cancer (PCa) mouse models. To clarify the association between gut microbiota and PCa in humans, we analyzed the gut microbiota profiles of men with suspected PCa. One hundred and fifty-two Japanese men undergoing prostate biopsies (96 with cancer and 56 without cancer) were included in the study and randomly divided into two cohorts: a discovery cohort (114 samples) and a test cohort (38 samples). The gut microbiota was compared between two groups, a high-risk group (men with Grade group 2 or higher PCa) and a negative + low-risk group (men with negative biopsy or Grade group 1 PCa), using 16S rRNA gene sequencing. The relative abundances of Rikenellaceae, Alistipes, and Lachnospira, all SCFA-producing bacteria, were significantly increased in high-risk group. In receiver operating characteristic curve analysis, the index calculated from the abundance of 18 bacterial genera which were selected by least absolute shrinkage and selection operator regression detected high-risk PCa in the discovery cohort with higher accuracy than the prostate specific antigen test (area under the curve [AUC] = 0.85 vs 0.74). Validation of the index in the test cohort showed similar results (AUC = 0.81 vs 0.67). The specific bacterial taxa were associated with high-risk PCa. The gut microbiota profile could be a novel useful marker for the detection of high-risk PCa and could contribute to the carcinogenesis of PCa.
Keywords:bacteria  biomarkers  gastrointestinal microbiome  metagenomics  prostate cancer
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号