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Prevalence of genotoxic bacteria in men undergoing biopsy for prostate cancer.
Lee, John; Wickes, Brian L; Fu, Jianmin; Brockman, Nohelli E; Garg, Harshit; Jobin, Christian; Johson-Pais, Teresa; Leach, Robin; Lai, Zhao; Liss, Michael A.
Afiliação
  • Lee J; Department of Urology, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Wickes BL; Department of Microbiology, Immunology, and Molecular Genetics, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Fu J; Department of Microbiology, Immunology, and Molecular Genetics, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Brockman NE; Department of Microbiology, Immunology, and Molecular Genetics, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Garg H; Department of Urology, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Jobin C; Division of Gastroenterology, Hepatology, and Nutrition, University of Florida College of Medicine, Gainesville, Florida, USA.
  • Johson-Pais T; Department of Urology, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Leach R; Department of Cell and Systems Biology, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Lai Z; Department of Molecular Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
  • Liss MA; Department of Urology, University of Texas Health San Antonio, San Antonio, Texas, USA.
Prostate ; 83(7): 663-669, 2023 05.
Article em En | MEDLINE | ID: mdl-36842100
ABSTRACT

BACKGROUND:

New evidence suggests that bacteria-produced DNA toxins may have a role in the development or progression of prostate cancer. To determine the prevalence of these genes in a noninfection (i.e., colonized) state, we screened urine specimens in men before undergoing a biopsy for prostate cancer detection.

METHODS:

We developed a multiplex polymerase chain reaction using three of the most described bacterial genotoxin gene primers Colibactin (polyketone synthase [pks] gene island clbN and clbB), cytotoxic necrotizing factor (cnf1) toxin, and cytolethal distending toxin B (cdtB) represented gene islands. After calibration on Escherichia coli samples of known genotypes, we used a training and validation cohort. We performed multiplex testing on a training cohort of previously collected urine from 45 men undergoing prostate biopsy. For the validation cohort, we utilized baseline urine samples from a previous randomized clinical trial (n = 263) with known prostate cancer outcomes.

RESULTS:

The prevalence of four common bacterial genotoxin genes detected in the urine before prostate biopsy for prostate cancer is 8% (25/311). The prevalence of pks island (clbN and clbB), cnf1, and cdt toxin genes are 6.1%, 2.4%, and 1.7%, respectively. We found no association between urinary genotoxins and prostate cancer (p = 0.83). We did identify a higher proportion of low-grade cancer (92% vs. 44%) in those men positive for urinary genotoxin and higher-grade cancer in those genotoxin negative (8% vs. 56%, p = 0.001).

CONCLUSIONS:

The prevalence of urinary genotoxins is low and does not correspond to a prostate cancer diagnosis. The urine was taken at one point in time and does not rule out the possibility of previous exposure.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article