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本文引用的文献

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A folic acid-enriched diet attenuates prostate involution in response to androgen deprivation.富含叶酸的饮食可减轻雄激素剥夺引起的前列腺退化。
Prostate. 2019 Feb;79(2):183-194. doi: 10.1002/pros.23723. Epub 2018 Oct 8.
2
Dysregulation and prognostic potential of 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and 5-carboxylcytosine (5caC) levels in prostate cancer.前列腺癌中 5-甲基胞嘧啶(5mC)、5-羟甲基胞嘧啶(5hmC)、5-甲酰胞嘧啶(5fC)和 5-羧基胞嘧啶(5caC)水平的失调及其预后潜力。
Clin Epigenetics. 2018 Aug 7;10(1):105. doi: 10.1186/s13148-018-0540-x.
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In vivo replacement of damaged bladder urothelium by Wolffian duct epithelial cells.体内 Wolffian 导管上皮细胞替代受损膀胱尿路上皮。
Proc Natl Acad Sci U S A. 2018 Aug 14;115(33):8394-8399. doi: 10.1073/pnas.1802966115. Epub 2018 Jul 30.
4
Altered DNA methyltransferases promoter methylation and mRNA expression are associated with tamoxifen response in breast tumors.DNA 甲基转移酶启动子甲基化和 mRNA 表达的改变与乳腺癌对他莫昔芬的反应相关。
J Cell Physiol. 2018 Sep;233(9):7305-7319. doi: 10.1002/jcp.26562. Epub 2018 Mar 25.
5
Androgenic to oestrogenic switch in the human adult prostate gland is regulated by epigenetic silencing of steroid 5α-reductase 2.成年男性前列腺中雄激素向雌激素的转变受甾体5α-还原酶2的表观遗传沉默调控。
J Pathol. 2017 Dec;243(4):457-467. doi: 10.1002/path.4985.
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Caloric restriction delays age-related methylation drift.热量限制延缓与年龄相关的甲基化漂移。
Nat Commun. 2017 Sep 14;8(1):539. doi: 10.1038/s41467-017-00607-3.
7
Loss of Gene Imprinting in Murine Prostate Promotes Widespread Neoplastic Growth.小鼠前列腺中基因印记的缺失促进广泛的肿瘤生长。
Cancer Res. 2017 Oct 1;77(19):5236-5247. doi: 10.1158/0008-5472.CAN-16-3089. Epub 2017 Aug 3.
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Genome-wide DNA methylation measurements in prostate tissues uncovers novel prostate cancer diagnostic biomarkers and transcription factor binding patterns.前列腺组织中的全基因组DNA甲基化测量揭示了新型前列腺癌诊断生物标志物和转录因子结合模式。
BMC Cancer. 2017 Apr 17;17(1):273. doi: 10.1186/s12885-017-3252-2.
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Genome-wide hepatic DNA methylation changes in high-fat diet-induced obese mice.高脂饮食诱导的肥胖小鼠肝脏全基因组DNA甲基化变化
Nutr Res Pract. 2017 Apr;11(2):105-113. doi: 10.4162/nrp.2017.11.2.105. Epub 2017 Mar 15.
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Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism.饮食限制可预防与年龄相关的DNA甲基化,并诱导脂质代谢的表观遗传重编程。
Genome Biol. 2017 Mar 28;18(1):56. doi: 10.1186/s13059-017-1187-1.

发育与疾病中的DNA甲基化:前列腺研究人员概述

DNA methylation in development and disease: an overview for prostate researchers.

作者信息

Joseph Diya B, Strand Douglas W, Vezina Chad M

机构信息

Department of Comparative Biosciences, University of Wisconsin-Madison Madison, WI 53706, USA.

Department of Urology, UT Southwestern Medical Center Dallas, TX 75390, USA.

出版信息

Am J Clin Exp Urol. 2018 Dec 20;6(6):197-218. eCollection 2018.

PMID:30697577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6334199/
Abstract

Epigenetic mechanisms including DNA methylation are critical regulators of organismal development and tissue homeostasis. DNA methylation is the transfer of methyl groups to cytosines, which adds an additional layer of complexity to the genome. DNA methylation marks are recognized by the cellular machinery to regulate transcription. Disruption of DNA methylation with aging or exposure to environmental toxins can change susceptibility to disease or trigger processes that lead to disease. In this review, we provide an overview of the DNA methylation machinery. More specifically, we describe DNA methylation in the context of prostate development, prostate cancer, and benign prostatic hyperplasia (BPH) as well as the impact of dietary and environmental factors on DNA methylation in the prostate.

摘要

包括DNA甲基化在内的表观遗传机制是机体发育和组织稳态的关键调节因子。DNA甲基化是甲基基团转移至胞嘧啶的过程,这为基因组增添了一层额外的复杂性。DNA甲基化标记可被细胞机制识别以调控转录。随着年龄增长或暴露于环境毒素而导致的DNA甲基化破坏,会改变疾病易感性或引发导致疾病的过程。在本综述中,我们概述了DNA甲基化机制。更具体地说,我们描述了前列腺发育、前列腺癌和良性前列腺增生(BPH)背景下的DNA甲基化,以及饮食和环境因素对前列腺DNA甲基化的影响。