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Environmental Toxicant Induced Epigenetic Transgenerational Inheritance of Prostate Pathology and Stromal-Epithelial Cell Epigenome and Transcriptome Alterations: Ancestral Origins of Prostate Disease

机译:前列腺病理学环境毒性诱导的表观遗传转化遗传和间质-上皮细胞表观基因组和转录组改变:前列腺疾病的祖先

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摘要

Prostate diseases include prostate cancer, which is the second most common male neoplasia, and benign prostatic hyperplasia (BPH), which affects approximately 50% of men. The incidence of prostate disease is increasing, and some of this increase may be attributable to ancestral exposure to environmental toxicants and epigenetic transgenerational inheritance mechanisms. The goal of the current study was to determine the effects that exposure of gestating female rats to vinclozolin has on the epigenetic transgenerational inheritance of prostate disease, and to characterize by what molecular epigenetic mechanisms this has occurred. Gestating female rats (F0 generation) were exposed to vinclozolin during E8-E14 of gestation. F1 generation offspring were bred to produce the F2 generation, which were bred to produce the transgenerational F3 generation. The transgenerational F3 generation vinclozolin lineage males at 12 months of age had an increased incidence of prostate histopathology and abnormalities compared to the control lineage. Ventral prostate epithelial and stromal cells were isolated from F3 generation 20-day old rats, prior to the onset of pathology, and used to obtain DNA and RNA for analysis. Results indicate that there were transgenerational changes in gene expression, noncoding RNA expression, and DNA methylation in both cell types. Our results suggest that ancestral exposure to vinclozolin at a critical period of gestation induces the epigenetic transgenerational inheritance of prostate stromal and epithelial cell changes in both the epigenome and transcriptome that ultimately lead to prostate disease susceptibility and may serve as a source of the increased incidence of prostate pathology observed in recent years.
机译:前列腺疾病包括前列腺癌和良性前列腺增生(BPH),前列腺癌是第二大最常见的男性赘生物,其影响大约50%的男性。前列腺疾病的发病率正在增加,其中某些增加可能归因于祖先接触环境毒物和表观遗传的世代遗传机制。本研究的目的是确定妊娠雌性大鼠暴露于长春新碱对前列腺疾病的表观遗传跨代遗传的影响,并通过这种分子表观遗传机制进行表征。妊娠雌性大鼠(F0代)在妊娠E8-E14期间暴露于Vinclozolin。繁殖F1代后代以产生F2代,然后繁殖以产生跨代F3代。与对照谱系相比,在12个月大的F3代长效Vinclozolin谱系男性具有更高的前列腺组织病理学和异常发生率。在病理学发作之前,从F3代20日龄大鼠中分离出前列腺前列腺上皮和基质细胞,并用于获得DNA和RNA用于分析。结果表明,在两种细胞类型中,基因表达,非编码RNA表达和DNA甲基化都有代际变化。我们的研究结果表明,在妊娠的关键时期祖先接触长春新唑啉可诱导表观基因组和转录组的前列腺基质和上皮细胞发生表观遗传的跨代遗传,最终导致前列腺疾病的易感性,并且可能是导致前列腺癌易感性增加的原因。近年来观察到前列腺病理。

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