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在生物体液中检测癌症特异性表观基因组变化:生物标志物发现和应用中的有力工具。

Detection of cancer-specific epigenomic changes in biofluids: powerful tools in biomarker discovery and application.

机构信息

Epigenetics Group, International Agency for Research on Cancer, 150 Cours Albert Thomas, 69372 Lyon, Cedex 08, France.

出版信息

Mol Oncol. 2012 Dec;6(6):704-15. doi: 10.1016/j.molonc.2012.07.005. Epub 2012 Aug 16.

Abstract

The genetic and epigenetic material originating from tumour that can be found in body fluids of individuals with cancer harbours tumour-specific alterations and represents an attractive target for biomarker discovery. Epigenetic changes (DNA methylation, histone modifications and non-coding RNAs) are present ubiquitously in virtually all types of human malignancies and may appear in early cancer development, and thus they provide particularly attractive markers with broad applications in diagnostics. In addition, because changes in the epigenome may constitute a signature of specific exposure to certain risk factors, they have the potential to serve as highly specific biomarkers for risk assessment. While reliable detection of cancer-specific epigenetic changes has proven to be technically challenging, a substantial progress has been made in developing the methodologies that allow an efficient and sensitive detection of epigenomic changes using the material originating from body fluids. In this review we discuss the application of epigenomics as a tool for biomarker research, with the focus on the analysis of DNA methylation in biofluids.

摘要

来自癌症患者体液中的肿瘤的遗传和表观遗传物质携带有肿瘤特异性的改变,是生物标志物发现的一个有吸引力的目标。表观遗传变化(DNA 甲基化、组蛋白修饰和非编码 RNA)普遍存在于几乎所有类型的人类恶性肿瘤中,并且可能出现在癌症早期发展中,因此它们提供了特别有吸引力的标记物,具有广泛的诊断应用。此外,由于表观基因组的改变可能构成特定暴露于某些危险因素的特征,因此它们有可能作为风险评估的高度特异性生物标志物。虽然已经证明可靠地检测癌症特异性的表观遗传变化具有技术挑战性,但在开发使用体液来源的材料进行高效和敏感的表观基因组变化检测的方法学方面已经取得了实质性进展。在这篇综述中,我们讨论了表观基因组学作为生物标志物研究工具的应用,重点是生物流体中 DNA 甲基化的分析。

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