Victor S Chen, Christopher James, Mark Khemmani, Shalin Desai, Chirag Doshi, Goran Rac, Jeffrey L Ellis, Hiten D Patel, Guliz A Barkan, Gopal N Gupta, Robert C Flanigan, Alan J Wolfe
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Patients were excluded if they had Prostate Imaging Reporting and Data System lesions with scores ≤ 3, a history of prostate biopsy within 1 year, a history of prostate cancer, or antibiotic use within 30 days of biopsy. Tissue was collected from the MRI target lesions and nonneoplastic transitional zone. Bacteria were identified using 16S ribosomal RNA gene sequencing.</p><p><strong>Results: </strong>Across the 42 patients, 76% were found to have prostate cancer. Beta diversity indices differed significantly between the perineum, voided urine, and prostate tissue. There were no beta diversity differences between cancerous or benign tissue, or between pre- and postbiopsy urines. There appear to be unique genera more abundant in cancerous versus benign tissue. 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引用次数: 0
摘要
背景:前列腺微生物群与前列腺癌之间的联系仍不清楚。对前列腺组织微生物群进行分析的研究很少,而且这些研究受到经直肠活检潜在污染的限制。经会阴前列腺活检是一种替代方法,可避免粪便交叉污染。我们的目的是利用经会阴前列腺活检来描述前列腺微生物组的特征:在 2022 年至 2023 年期间,我们对临床怀疑患有前列腺癌的患者进行了前瞻性登记,这些患者将在磁共振成像(MRI)融合引导下接受经会阴前列腺活检。如果患者的前列腺成像报告和数据系统(Prostate Imaging Reporting and Data System)病灶评分≤3分、1年内有前列腺活检史、前列腺癌史或在活检后30天内使用过抗生素,则排除在外。从核磁共振成像目标病灶和非肿瘤性过渡区采集组织。通过 16S 核糖体 RNA 基因测序鉴定细菌:结果:42 名患者中,76% 发现患有前列腺癌。会阴部、排出的尿液和前列腺组织的贝塔多样性指数差异显著。癌组织和良性组织之间以及活检前尿液和活检后尿液之间没有贝塔多样性差异。与良性组织相比,癌症组织中似乎有更多的独特种属。α多样性指数与临床结果(包括癌症状态、等级和风险组别)之间没有差异:我们展示了一种严格的方法,可通过经会阴活检更好地确定前列腺微生物组的特征并限制污染。这些发现为今后大规模研究前列腺癌微生物组提供了一个框架。
A prospective evaluation of the prostate microbiome in malignant and benign tissue using transperineal biopsy.
Background: The link between the prostate microbiome and prostate cancer remains unclear. Few studies have analyzed the microbiota of prostate tissue, and these have been limited by potential contamination by transrectal biopsy. Transperineal prostate biopsy offers an alternative and avoids fecal cross-contamination. We aim to characterize the prostate microbiome using transperineal biopsy.
Methods: Patients with clinical suspicion for prostate cancer who were to undergo transperineal prostate biopsy with magnetic resonance imaging (MRI) fusion guidance were prospectively enrolled from 2022 to 2023. Patients were excluded if they had Prostate Imaging Reporting and Data System lesions with scores ≤ 3, a history of prostate biopsy within 1 year, a history of prostate cancer, or antibiotic use within 30 days of biopsy. Tissue was collected from the MRI target lesions and nonneoplastic transitional zone. Bacteria were identified using 16S ribosomal RNA gene sequencing.
Results: Across the 42 patients, 76% were found to have prostate cancer. Beta diversity indices differed significantly between the perineum, voided urine, and prostate tissue. There were no beta diversity differences between cancerous or benign tissue, or between pre- and postbiopsy urines. There appear to be unique genera more abundant in cancerous versus benign tissue. There were no differences in alpha diversity indices relative to clinical findings including cancer status, grade, and risk group.
Conclusions: We demonstrate a rigorous method to better characterize the prostate microbiome using transperineal biopsy and to limit contamination. These findings provide a framework for future large-scale studies of the microbiome of prostate cancer.
期刊介绍:
The Prostate is a peer-reviewed journal dedicated to original studies of this organ and the male accessory glands. It serves as an international medium for these studies, presenting comprehensive coverage of clinical, anatomic, embryologic, physiologic, endocrinologic, and biochemical studies.