Suppr超能文献

癌症中 microRNA 表达的表观遗传调控

Epigenetic regulation of microRNA expression in cancer.

作者信息

Choudhry Hani, Catto James W F

机构信息

Academic Urology Unit, Division of Clinical Sciences, Royal Hallamshire Hospital, University of Sheffield, Sheffield, UK.

出版信息

Methods Mol Biol. 2011;676:165-84. doi: 10.1007/978-1-60761-863-8_12.

Abstract

Epigenetic gene regulation is important in human cancer. Both functional and observational data implicate alterations of histone modifications, DNA promoter methylation, and non-coding RNA expression in carcinogenic roles. We sought to explore the role of aberrant DNA hypermethylation in the regulation of microRNA (miR) expression in human cancer. From human genome databases we calculated that 13 and 28% of human miR genes are located within 3 and 10 kb of a CpG island, respectively. To identify miRs that are regulated by epigenetic mechanisms in cancer, we performed expression profiling prior to and following treatment of cell lines with 5-azacytidine. We used oligonucleotide microarrays to determine miR expression. For miRs whose expression changed following 5-azacytidine treatment, we sequenced the adjacent CpG island and promoter using bisulphite-treated DNA. Here, we describe these methods to enable other researchers to use this approach.

摘要

表观遗传基因调控在人类癌症中具有重要意义。功能数据和观察数据均表明,组蛋白修饰、DNA启动子甲基化及非编码RNA表达的改变在致癌过程中发挥作用。我们试图探究异常DNA高甲基化在人类癌症中对微小RNA(miR)表达调控的作用。通过人类基因组数据库,我们计算得出分别有13%和28%的人类miR基因位于CpG岛的3 kb和10 kb范围内。为了鉴定癌症中受表观遗传机制调控的miR,我们在用5-氮杂胞苷处理细胞系前后进行了表达谱分析。我们使用寡核苷酸微阵列来确定miR表达。对于那些在5-氮杂胞苷处理后表达发生变化的miR,我们使用亚硫酸氢盐处理的DNA对相邻的CpG岛和启动子进行测序。在此,我们描述这些方法,以便其他研究人员能够采用这种方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验