Departments of Urology, Physiology and Pathology, College of Medicine, University of Illinois at Chicago, 820 S Wood Street, MC955, Chicago, 60612, IL, USA.
Differentiation. 2021 Mar-Apr;118:72-81. doi: 10.1016/j.diff.2020.12.001. Epub 2021 Jan 7.
While estrogens are involved in normal prostate morphogenesis and function, inappropriate early-life estrogenic exposures, either in type, dose or timing, can reprogram the prostate gland and lead to increased disease risk with aging. This process is referred to as estrogen imprinting or developmental estrogenization of the prostate gland. The present review discusses published and new evidence for prostatic developmental estrogenization that includes extensive research in rodent models combined with epidemiology findings that together have helped to uncover the architectural and molecular underpinnings that promote this phenotype. Complex interactions between steroid receptors, developmental morphoregulatory factors, epigenetic machinery and stem-progenitor cell targets coalesce to hard wire structural, cellular and epigenomic reorganization of the tissue which retains a life-long memory of early-life estrogens, ultimately predisposing the gland to prostatitis, hyperplasia and carcinogenesis with aging.
虽然雌激素参与了正常前列腺的形态发生和功能,但不合适的早期生命雌激素暴露,无论是类型、剂量还是时间,都可能重新编程前列腺,并随着年龄的增长增加疾病风险。这个过程被称为前列腺的雌激素印迹或发育性雌激素化。本综述讨论了已发表的和新的前列腺发育性雌激素化的证据,包括对啮齿动物模型的广泛研究以及流行病学发现,这些研究共同揭示了促进这种表型的结构和分子基础。甾体受体、发育形态调节因子、表观遗传机制和干细胞-祖细胞靶标之间的复杂相互作用,共同导致组织的结构、细胞和表观基因组的重新组织,这种组织保留了对早期生命雌激素的终生记忆,最终使前列腺容易发生前列腺炎、增生和癌变。