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表观遗传生物标志物在人类疾病早期诊治中的研究进展

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  • 1. 武汉大学中南医院骨科,武汉 430071
    2.武汉大学基础医学院药理学系,武汉 430071
    3. 湖北省发育源性疾病重点实验室,武汉 430071
作者简介: 黎伟,硕士研究生,专业方向:骨关节病。E-mail: 444069914@qq.com|通讯作者: 秦俊,博士,主治医师,专业方向:骨关节病。E-mail: heart. blue@163.com

收稿日期: 2017-10-16

  修回日期: 2018-01-03

  网络出版日期: 2018-02-01

基金资助

国家自然科学基金项目(81220108026,81401832)

Research progress of epigenetic biomarkers in the early diagnosis and treatment of human diseases

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  • 1. Department of Orthopedics, Zhongnan Hospital of Wuhan University, Wuhan 430071, China
    2. Department of Pharmacology, Basic Medical School of Wuhan University, Wuhan 430071, China
    3. Hubei Provincial Key Laboratory of Developmentally Originated Disease, Wuhan 430071, China

Received date: 2017-10-16

  Revised date: 2018-01-03

  Online published: 2018-02-01

Supported by

the National Natural Science Foundation of China(81220108026,81401832)

摘要

表观遗传修饰异常见于人类的多种疾病(如肿瘤、老年性疾病、发育源性疾病等),影响着这些疾病的发生发展。已有的研究表明,异常表观遗传改变可以作为疾病状态和疾病预测的生物标志物。表观遗传修饰改变的可逆性和可控性也为疾病早期的预防和治疗提供了新策略。本文对DNA甲基化修饰、组蛋白共价修饰、非编码RNA等三种表观遗传方式在肿瘤、老年性疾病和发育源性疾病的研究,以及三者作为表遗传生物标志物在疾病早期诊断和治疗的应用展开介绍,以期为肿瘤、老年性和发育源性相关疾病的诊断与治疗提供借鉴和 参考。

本文引用格式

黎伟, 秦俊, 汪晖, 陈廖斌 . 表观遗传生物标志物在人类疾病早期诊治中的研究进展[J]. 遗传, 2018 , 40(2) : 104 -115 . DOI: 10.16288/j.yczz.17-220

Abstract

Abnormal epigenetic modifications are common in many diseases (such as tumors, senile and developmental diseases), and can influence the pathogenesis and progression of these diseases. Various studies demonstrated that abnormal epigenetic changes could be used as biomarkers for diagnosis of the disease status and prognosis of disease progression. The reversibility and controllability of epigenetic modifications also offer an opportunity to develop new strategies for the early prevention and treatment of diseases. In this review, we provide a brief overview of the latest discoveries in three areas of epigenetic research, i.e., DNA methylation, histone modifications and non-coding RNAs, and their potential applications in early diagnosis and treatment of tumors, senile and developmental diseases. We hope to provide some insights and references in developing strategies for the diagnosis and treatment of these diseases.

参考文献

[1] Prins GS, Ye SH, Birch L, Zhang X, Cheong A, Lin H, Calderon-Gierszal E, Groen J, Hu WY, Ho SM, Van Breemen RB . Prostate cancer risk and DNA methylation signatures in aging rats following developmental BPA Exposure: a dose-response analysis. Environ Health Perspect, 2017, 125(7):077007.
[2] Graca I, Pereira-Silva E, Henrique R, Packham G, Crabb SJ, Jeronimo C . Epigenetic modulators as therapeutic targets in prostate cancer. Clin Epigenetics, 2016, 8(1):98.
[3] Tahara T, Tahara S, Horiguchi N, Kawamura T, Okubo M, Yamada H, Yoshida D, Ohmori T, Maeda K, Komura N, Ikuno H, Jodai Y, Kamano T, Nagasaka M, Nakagawa Y, Tsukamoto T, Urano M, Shibata T, Kuroda M, Ohmiya N . Methylation status of IGF2 DMR and LINE1 in leukocyte DNA provides distinct clinicopathological features of gastric cancer patients. Clin Exp Med, 2017. DOI: 10.1007/s10238-017-0471-4.
[4] Moruzzi S, Guarini P, Udali S, Ruzzenente A, Guglielmi A, Conci S, Pattini P, Martinelli N, Olivieri O, Tammen S A, Choi S W, Friso S . One-carbon genetic variants and the role of MTHFD1 1958G>A in liver and colon cancer risk according to global DNA methylation. PLoS One, 2017, 12(10):e0185792.
[5] Iwata A, Nagata K, Hatsuta H, Takuma H, Bundo M, Iwamoto K, Tamaoka A, Murayama S, Saido T, Tsuji S . Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulation. Hum Mol Genet, 2014, 23(3):648-656.
[6] Lee J, Hagerty S, Cormier KA, Kim J, Kung AL, Ferrante RJ, Ryu H . Monoallele deletion of CBP leads to pericentromeric heterochromatin condensation through ESET expression and histone H3(K9) methylation. Hum Mol Genet, 2008, 17(12):1774-1782.
[7] Begum G, Davies A, Stevens A, Oliver M, Jaquiery A, Challis J, Harding J, Bloomfield F, White A . Maternal undernutrition programs tissue-specific epigenetic changes in the glucocorticoid receptor in adult offspring. Endocrinology, 2013, 154(12):4560-4569.
[8] Baserga M, Kaur R, Hale MA, Bares A, Yu X, Callaway CW , McKnight RA, Lane RH. Fetal growth restriction alters transcription factor binding and epigenetic mechanisms of renal 11β-hydroxysteroid dehydrogenase type 2 in a sex-specific manner. Am J Physiol Regul Integr Comp Physiol, 2010, 299(1):R334-R342.
[9] Baserga M, Hale MA, Wang ZM , YuX, Callaway CW, McKnight RA, Lane RH. Uteroplacental insufficiency alters nephrogenesis and downregulates cyclooxygenase-2 expression in a model of IUGR with adult-onset hypertension. Am J Physiol Regul Integr Comp Physiol, 2007, 292(5):R1943-R1955.
[10] Masuyama H, Hiramatsu Y . Effects of a high-fat diet exposure in utero on the metabolic syndrome-like phenomenon in mouse offspring through epigenetic changes in adipocytokine gene expression. Endocrinology, 2012, 153(6):2823-2830.
[11] Li D, Tian YJ, Guo J, Sun WP, Lun YZ, Guo M, Luo N, Cao Y, Cao JM, Gong XJ, Zhou SS . Nico
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