Diet and the microbiome as mediators of prostate cancer risk, progression, and therapy response

被引:0
|
作者
Cruz-Lebron, Angelica
Faiez, Tasnim Syakirah [1 ]
Hess, Megan M. [1 ]
Sfanos, Karen S. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21218 USA
[2] Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21218 USA
关键词
Prostate cancer; diet; microbiome; inflammation; infection; metabolites; DOUBLE-STRAND BREAKS; PHIP-DNA ADDUCTS; INTESTINAL MICROBIOTA; METABOLIC-ACTIVATION; GUT MICROBIOTA; IN-VIVO; S-PHASE; GROWTH; EQUOL; RECEPTOR;
D O I
10.1016/j.urolonc.2024.12.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Complex relationships between the human microbiome and cancer are increasingly recognized for cancer sites that harbor commensal microbial communities such as the gut, genitourinary tract, and skin. For organ sites that likely do not contain commensal microbiota, there is still a substantial capacity for the human-associated microbiota to influence disease etiology across the cancer spectrum. We propose such a relationship for prostate cancer, the most commonly diagnosed cancer in males in the United States. This review explores the current evidence for a role for the urinary and gut microbiota in prostate cancer risk, via both direct interactions (prostate infections) and long-distance interactions such as via the metabolism of procarcinogenic or anticarcinogenic dietary metabolites. We further explore a newly recognized role of the gut microbiota in mediating cancer treatment response or resistance either via production of androgens and/or procarcinogenic metabolites or via direct metabolism of anticancer drugs that are used to treat advanced disease. Overall, we present the current state of knowledge relating to how the human microbiome mediates prostate cancer risk, progression, and therapy response, as well as suggest future research directions for the field. (c) 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:209 / 220
页数:12
相关论文
共 50 条
  • [1] Microbiome in cancer progression and therapy
    Andreeva, Natalia V.
    Gabbasova, Railia R.
    Grivennikov, Sergei I.
    CURRENT OPINION IN MICROBIOLOGY, 2020, 56 : 118 - 126
  • [2] The Microbiome and Prostate Cancer Risk
    Wheeler, Karen M.
    Liss, Michael A.
    CURRENT UROLOGY REPORTS, 2019, 20 (10)
  • [3] The evolving role of diet in prostate cancer risk and progression
    Kaiser, Adeel
    Haskins, Christopher
    Siddiqui, Mohummad M.
    Hussain, Arif
    D'Adamo, Christopher
    CURRENT OPINION IN ONCOLOGY, 2019, 31 (03) : 222 - 229
  • [4] Understanding the microbiome as a mediator of bladder cancer progression and therapeutic response
    Golshani, Mahgol
    Taylor III, John A.
    Woolbright, Benjamin L.
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2025, 43 (04) : 254 - 265
  • [5] The human microbiome and its link in prostate cancer risk and pathogenesis
    Katongole, Paul
    Sande, Obondo J.
    Joloba, Moses
    Reynolds, Steven J.
    Niyonzima, Nixon
    INFECTIOUS AGENTS AND CANCER, 2020, 15 (01)
  • [6] The Microbiome of Prostate Fluid Is Associated With Prostate Cancer
    Ma, Xiaowei
    Chi, Chenfei
    Fan, Liancheng
    Dong, Baijun
    Shao, Xiaoguang
    Xie, Shaowei
    Li, Min
    Xue, Wei
    FRONTIERS IN MICROBIOLOGY, 2019, 10
  • [7] Obesity, dietary interventions and microbiome alterations in the development and progression of prostate cancer
    Trecarten, Shaun
    Liss, Michael A.
    Hamilton-Reeves, Jill
    Digiovanni, John
    FRONTIERS IN IMMUNOLOGY, 2025, 15
  • [8] MICROBIOME AND PROSTATE CANCER
    Marekovic, Ivana
    ACTA CLINICA CROATICA, 2024, 63 : 56 - 62
  • [9] Microbiome and Diet in Colon Cancer Development and Treatment
    Kato, Ikuko
    Sun, Jun
    CANCER JOURNAL, 2023, 29 (02) : 89 - 97
  • [10] Chronic inflammatory mediators enhance prostate cancer development and progression
    Thapa, Dinesh
    Ghosh, Rita
    BIOCHEMICAL PHARMACOLOGY, 2015, 94 (02) : 53 - 62