The Role of Gut Microbiome in the Pathogenesis of Prostate Cancer: A Prospective, Pilot Study

医学 前列腺癌 肠道微生物群 发病机制 微生物群 癌症 前列腺疾病 前瞻性队列研究 肿瘤科 生物信息学 前列腺 内科学 肠道菌群 免疫学 生物
作者
David Golombos,Abimbola Ayangbesan,Padraic O’Malley,Patrick Lewicki,LaMont Barlow,Christopher E. Barbieri,Chrystal Chan,Casey DuLong,Galeb Abu-Ali,Curtis Huttenhower,Douglas S. Scherr
出处
期刊:Urology [Elsevier]
卷期号:111: 122-128 被引量:170
标识
DOI:10.1016/j.urology.2017.08.039
摘要

Objective

To elucidate potential biomarkers or mechanistic principles involved with the gut microbiota and its impact on prostate cancer pathogenesis.

Materials and Methods

We performed a prospective case-control pilot study evaluating the gut microbiome of 20 men with either benign prostatic conditions (n = 8) or intermediate or high risk clinically localized prostate cancer (Gleason ≥4 + 3 cN0M0) (n = 12) undergoing care at tertiary referral center from September 1, 2015 to March 1, 2016. Key exclusion criteria included recent antibiotic use, significant gastrointestinal disorders, hormonal or systemic therapy for prostate cancer. Computational genomics analysis was performed on collected stool samples using MetaPhlAn2 and HUMAnN2 platforms. Linear discriminant analysis effect size method was used to support high-dimensional class comparisons to find biologically relevant features. Kruskal-Wallis sum-rank test was used to detect features with significant differential abundance with respect to class, with biological consistency investigated using a set of pairwise tests among subclasses using the Wilcoxon rank-sum test, both to an α ≤0.05.

Results

Higher relative abundance of Bacteriodes massiliensis was seen in prostate cancer cases compared to controls. Faecalibacterium prausnitzii and Eubacterium rectalie had higher relative abundance among controls. Biologically significant differences were also found in relative gene, pathway, and enzyme abundance.

Conclusion

Biologically significant differences exist in the gut microbial composition of men with prostate cancer compared to benign controls. These differences may play a role in the pathobiology of prostate cancer, and warrant further exploration.
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