癌症表观基因组学综述

Robby Kumar, N. Sharan
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引用次数: 1

摘要

对控制正常细胞生长至关重要的基因的表观遗传失活是癌细胞的标志。DNA的表观遗传修饰不改变核苷酸序列,而是涉及基因转录和DNA甲基化的调节。肿瘤抑制基因启动子内的超甲基化或组蛋白去乙酰化会导致该基因的沉默、缺失或突变。癌细胞经常表现出异常的甲基化,并且随着疾病的进展,异常的频率增加。高甲基化事件可发生在肿瘤发生的早期,涉及可能使细胞易发生恶性转化的途径的破坏。表观遗传修饰如DNA甲基化可以用于癌症患者的临床目的,首先使用超甲基化作为癌细胞的分子生物标志物,其次,表观遗传改变可能是可逆的。
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Cancer Epigenomics: a review
Epigenetic inactivation of genes that are crucial for the control of normal cell growth is a hallmark of cancer cells. Epigenetic modifications of the DNA do not alter the nucleotide sequence instead they involve the regulation of gene transcription and DNA methylation. Hypermethylation or histone deacetylation, which is within the promoter of a tumor suppressor gene, leads to the silencing as well as a deletion or a mutation of that gene. Cancer cells often show aberrant methylation and the frequency of aberrations increases is seen with the progression of disease. Hypermethylation events can occur early in tumorogenesis, involving the disruption of pathways that may predispose cells to malignant transformation. Epigenetic modification such as DNA methylation can be exploited for clinical purposes in cancer patients, first using hypermethylation as a molecular biomarker of cancer cells and second, epigenetic changes which are potentially reversible.
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