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表观基因组学与卵巢癌。

Epigenomics and ovarian carcinoma.

机构信息

Department of Otolaryngology & Head & Neck Surgery, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, Maryland 21231, USA.

出版信息

Biomark Med. 2010 Aug;4(4):543-70. doi: 10.2217/bmm.10.72.

DOI:10.2217/bmm.10.72
PMID:20701443
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4441332/
Abstract

Ovarian cancer is the leading cause of death among gynecological cancers. It is now recognized that in addition to genetic alterations, epigenetic mechanisms, such as DNA methylation, histone modifications and nucleosome remodeling, play an important role in the development and progression of ovarian cancer by modulating chromatin structure, and gene and miRNA expression. Furthermore, epigenetic alterations have been recognized as useful tools for the development of novel biomarkers for diagnosis, prognosis, therapeutic prediction and monitoring of diseases. Moreover, new epigenetic therapies, such as DNA methyltransferase inhibitors and histone deacetylase inhibitors, have been found to be a potential therapeutic option, especially when used in combination with other agents. Here we discuss current developments in ovarian carcinoma epigenome research, the importance of the ovarian carcinoma epigenome for development of diagnostic and prognostic biomarkers, and the current epigenetic therapies used in ovarian cancer.

摘要

卵巢癌是妇科癌症死亡的主要原因。现在人们认识到,除了遗传改变外,表观遗传机制,如 DNA 甲基化、组蛋白修饰和核小体重塑,通过调节染色质结构以及基因和 miRNA 表达,在卵巢癌的发生和发展中发挥重要作用。此外,表观遗传改变已被认为是开发用于疾病诊断、预后、治疗预测和监测的新型生物标志物的有用工具。此外,发现新的表观遗传疗法,如 DNA 甲基转移酶抑制剂和组蛋白去乙酰化酶抑制剂,是一种潜在的治疗选择,尤其是与其他药物联合使用时。本文讨论了卵巢癌表观基因组研究的最新进展、卵巢癌表观基因组在开发诊断和预后生物标志物方面的重要性,以及目前用于卵巢癌的表观遗传疗法。

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本文引用的文献

1
Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
2
Genome-wide DNA methylation analysis of archival formalin-fixed paraffin-embedded tissue using the Illumina Infinium HumanMethylation27 BeadChip.基于 Illumina Infinium HumanMethylation27 BeadChip 的存档福尔马林固定石蜡包埋组织的全基因组 DNA 甲基化分析。
Methods. 2010 Nov;52(3):248-54. doi: 10.1016/j.ymeth.2010.04.012. Epub 2010 Apr 29.
3
Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma.鉴定出一种 CpG 岛甲基化表型,它定义了神经胶质瘤的一个独特亚群。
Cancer Cell. 2010 May 18;17(5):510-22. doi: 10.1016/j.ccr.2010.03.017. Epub 2010 Apr 15.
4
Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents.临床试验中的新型组蛋白去乙酰化酶抑制剂作为抗癌药物。
J Hematol Oncol. 2010 Feb 4;3:5. doi: 10.1186/1756-8722-3-5.
5
Methylation analysis by DNA immunoprecipitation.通过 DNA 免疫沉淀进行甲基化分析。
J Cell Physiol. 2010 Mar;222(3):522-31. doi: 10.1002/jcp.22009.
6
Solving the Dnmt2 enigma.解开Dnmt2之谜。
Chromosoma. 2010 Feb;119(1):35-40. doi: 10.1007/s00412-009-0240-6.
7
DNA methylation analysis in liquid-based cytology for cervical cancer screening.用于宫颈癌筛查的液基细胞学中的DNA甲基化分析。
Int J Cancer. 2009 Dec 15;125(12):2995-3002. doi: 10.1002/ijc.24745.
8
Combined inhibition of DNA methylation and histone acetylation enhances gene re-expression and drug sensitivity in vivo.DNA甲基化和组蛋白乙酰化的联合抑制增强了体内基因的重新表达和药物敏感性。
Br J Cancer. 2009 Mar 10;100(5):758-63. doi: 10.1038/sj.bjc.6604932.
9
MicroRNAs and their target messenger RNAs associated with ovarian cancer response to chemotherapy.与卵巢癌化疗反应相关的微小RNA及其靶信使核糖核酸
Gynecol Oncol. 2009 May;113(2):249-55. doi: 10.1016/j.ygyno.2009.01.014. Epub 2009 Feb 23.
10
The promises and pitfalls of epigenetic therapies in solid tumours.实体瘤表观遗传疗法的前景与陷阱
Eur J Cancer. 2009 May;45(7):1129-1136. doi: 10.1016/j.ejca.2009.01.003. Epub 2009 Feb 11.