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Microbiome signatures in prostate cancer.
Banerjee, Sagarika; Alwine, James C; Wei, Zhi; Tian, Tian; Shih, Natalie; Sperling, Colin; Guzzo, Thomas; Feldman, Michael D; Robertson, Erle S.
Affiliation
  • Banerjee S; Department of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
  • Alwine JC; Department of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Wei Z; Department of Computer Science, New Jersey Institute of Technology, Newark, NJ, USA.
  • Tian T; Department of Computer Science, New Jersey Institute of Technology, Newark, NJ, USA.
  • Shih N; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Sperling C; Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Guzzo T; Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Feldman MD; Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Robertson ES; Department of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Carcinogenesis ; 40(6): 749-764, 2019 07 06.
Article in En | MEDLINE | ID: mdl-30794288
We have established a microbiome signature for prostate cancer using an array-based metagenomic and capture-sequencing approach. A diverse microbiome signature (viral, bacterial, fungal and parasitic) was observed in the prostate cancer samples compared with benign prostate hyperplasia controls. Hierarchical clustering analysis identified three distinct prostate cancer-specific microbiome signatures. The three signatures correlated with different grades, stages and scores of the cancer. Thus, microbiome signature analysis potentially provides clinical diagnosis and outcome predictions. The array data were validated by PCR and targeted next-generation sequencing (NGS). Specific NGS data suggested that certain viral genomic sequences were inserted into the host somatic chromosomes of the prostate cancer samples. A randomly selected group of these was validated by direct PCR and sequencing. In addition, PCR validation of Helicobacter showed that Helicobacter cagA sequences integrated within specific chromosomes of prostate tumor cells. The viral and Helicobacter integrations are predicted to affect the expression of several cellular genes associated with oncogenic processes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Microbiota Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Carcinogenesis Year: 2019 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Microbiota Type of study: Prognostic_studies Limits: Humans / Male Language: En Journal: Carcinogenesis Year: 2019 Type: Article Affiliation country: United States