表观遗传学
医学
重编程
DNA甲基化
小RNA
癌症研究
表观遗传疗法
疾病
体细胞
肿瘤科
组蛋白
肾细胞癌
生物信息学
生物
病理
细胞
遗传学
基因表达
DNA
基因
作者
Sophie C. Joosten,Kim M. Smits,Maureen J.B. Aarts,Veerle Melotte,Alexander Koch,Vivianne C. G. Tjan‐Heijnen,Manon van Engeland
标识
DOI:10.1038/s41585-018-0023-z
摘要
Renal cell carcinoma (RCC) is characterized by an infrequent number of somatic mutations. By contrast, epigenetic aberrations are commonly found in RCC, indicating that epigenetic reprogramming is an important event in RCC development. Epigenetic alterations comprise several different aberrations, such as changes in histone modifications, DNA methylation, and microRNA levels, and occur in the most important signalling pathways in RCC, such as the von Hippel-Lindau disease tumour suppressor (VHL)-hypoxia-inducible factor (HIF) pathway, the WNT-β-catenin pathway, and pathways involved in epithelial-mesenchymal transition. Owing to their involvement in these pathways and frequent occurrence in RCC, epigenetic alterations are regarded as potential biomarkers for the early detection of disease and for prediction of prognosis and treatment response. In addition, most of these alterations are potentially reversible, so they also provide new targets for therapy. At the moment, epigenetic biomarkers for RCC are not being used in clinical practice, but targeted epigenetic therapies are under investigation. Understanding the extent of epigenetic changes occurring in RCC and the mechanisms by which they influence disease progression and treatment response, as well as knowledge of current research on biomarkers and treatments, is crucial to successful clinical translation of epigenetics in RCC.
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