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The gut microbiome is formed by a vast and diverse community of bacteria that colonizes our large intestine. These bacteria start residing in the gut from birth and continue diversifying throughout life, influenced by factors such as diet, lifestyle, and stress. The gut bacterial community also includes bacteria from food and those that enter the colon through the anus.
The normal gut flora of the colon plays a critical role in generating essential vitamins such as vitamins K, B5, and B7.
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Correction: Peptine et al. Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA) and Vancomycin-Resistant Enterococci (VRE) in Nosocomial Infections: A Systematic Review of Resistance, Pathogenesis, and Clinical Management. <i>Microorganisms</i> 2026, <i>14</i>, 428.

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Exploring the Intestinal Microbiota Profile in Prostate Cancer Patients and Healthy Controls.

Giovanna Cocomazzi1, Annacandida Villani1, Gandino Mencarelli2

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This summary is machine-generated.

Gut bacteria differ between prostate cancer patients and healthy individuals. Specific bacteria like Lactobacillus and Collinsella may serve as future biomarkers for prostate cancer diagnosis and prognosis.

Keywords:
16S rRNA gene sequencingbacterial signaturefunctional predictiongut microbiotaprostate cancer

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Area of Science:

  • Microbiology
  • Oncology
  • Gastroenterology

Background:

  • Prostate cancer (PCa) is a common male neoplasm.
  • Gut microbiota's role in PCa onset, progression, and prognosis is increasingly recognized.
  • Prostate-specific antigen (PSA) testing for PCa screening has limited specificity.

Purpose of the Study:

  • Investigate gut microbiota differences between PCa patients and healthy controls (HCs).
  • Identify bacterial biomarkers for PCa diagnosis and prognosis.
  • Correlate gut microbes with clinical laboratory parameters in PCa evaluation.

Main Methods:

  • 16S rRNA gene sequencing of fecal DNA from 18 PCa patients and 18 HCs.
  • Analysis of gut microbial profiles, including diversity and functional predictions.
  • Recursive partitioning tree for bacterial signature identification and correlation analysis.

Main Results:

  • Significant differences in gut microbiota composition and diversity (alpha, beta) between PCa patients and HCs.
  • Enriched microbial pathways in PCa patients include Krebs cycle and steroid hormone synthesis.
  • A bacterial signature of Lactobacillus and Collinsella distinguished PCa from HCs, with significant correlations to clinical parameters.

Conclusions:

  • Gut microbiota profiles show potential as future biomarkers for prostate cancer risk and progression.
  • Specific bacterial signatures, like Lactobacillus and Collinsella, may aid in PCa diagnosis.
  • Further prospective studies and clinical validation are necessary before implementing these as diagnostic or prognostic tools.