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The role of gut microbiota in prostate cancer progression: A Mendelian randomization study of immune mediation.
Li, Song; Liu, Ruoxuan; Hao, Xuexue; Liu, Xiaoqiang.
Afiliação
  • Li S; Department of Urology, Tianjin Medical University General Hospital, Tianjin, China.
  • Liu R; Department of Urology, Huaihe Hospital of Henan University, Kaifeng, China.
  • Hao X; Plastic Surgery Department, Henan International Joint Laboratory of Cellular Medical Engineering, Henan, China.
  • Liu X; Department of Urology, Huaihe Hospital of Henan University, Kaifeng, China.
Medicine (Baltimore) ; 103(27): e38825, 2024 Jul 05.
Article em En | MEDLINE | ID: mdl-38968485
ABSTRACT
The potential relationship between the gut microbiota and prostate cancer, possibly influenced by immune cells, remains unclear. This study employed the mediation Mendelian randomization (MR) technique to investigate the causal link between the gut microbiota, immune cells, and prostate cancer. Data on immune cell activity were sourced from Valeria Orrù's research, whereas the genome-wide association study outcome dataset was obtained from the Integrative Epidemiology Unit database. The bidirectional MR analysis utilized 5 different

methods:

inverse variance weighted (IVW), weighted median, MR-Egger regression, weighted mode, and simple mode. In addition, the mediating effect of immune cells on the gut microbiota and prostate cancer was explored using mediation analysis. Eighty-three single nucleotide polymorphisms associated with prostate cancer were screened as instrumental variables. In a positive MR analysis with gut microbiota as the exposure factor, IVW showed an association between 8 gut microbiota and prostate cancer. Additionally, 9 types of immune cells have been found to be associated with prostate cancer using methods such as IVW. MR analysis of the gut microbiota on immune cells (beta1) revealed a negative correlation between Bifidobacterium and CD39+ T regulatory cells (Tregs; odds ratio [OR] = 0.785, 95% confidence interval [CI] = 0.627-0.983, P = .03). Furthermore, MR analysis of immune cells in prostate cancer disease (beta2) showed that CD39+Tregs are a risk factor for prostate cancer (OR = 1.215, 95% CI = 1.027-1.354, P = .04). Moreover, MR analysis of gut microbiota in prostate cancer (total effect) indicated that Bifidobacterium is a protective factor for prostate cancer (OR = 0.905, 95% CI = 0.822-0.977, P = .04). The sensitivity analysis verified the robustness of the above results. Mediation analysis demonstrated that CD39+Tregs partially mediate the causal relationship between Bifidobacterium and prostate cancer. This study demonstrates that Bifidobacterium inhibits prostate cancer progression through CD39+Tregs as mediators, providing new ideas and approaches for the treatment and prevention of prostate cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Progressão da Doença / Polimorfismo de Nucleotídeo Único / Análise da Randomização Mendeliana / Microbioma Gastrointestinal Limite: Humans / Male Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Progressão da Doença / Polimorfismo de Nucleotídeo Único / Análise da Randomização Mendeliana / Microbioma Gastrointestinal Limite: Humans / Male Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China