Micevic Goran, Theodosakis Nicholas, Bosenberg Marcus
Department of Dermatology, Yale University School of Medicine, New Haven, CT 06520 USA.
Department of Pathology, Yale University School of Medicine, New Haven, CT 06520 USA.
Clin Epigenetics. 2017 Apr 4;9:34. doi: 10.1186/s13148-017-0332-8. eCollection 2017.
Aberrant DNA methylation is an epigenetic hallmark of melanoma, known to play important roles in melanoma formation and progression. Recent advances in genome-wide methylation methods have provided the means to identify differentially methylated genes, methylation signatures, and potential biomarkers. However, despite considerable effort and advances in cataloging methylation changes in melanoma, many questions remain unanswered. The aim of this review is to summarize recent developments, emerging trends, and important unresolved questions in the field of aberrant DNA methylation in melanoma. In addition to reviewing recent developments, we carefully synthesize the findings in an effort to provide a framework for understanding the current state and direction of the field. To facilitate clarity, we divided the review into DNA methylation changes in melanoma, biomarker opportunities, and therapeutic developments. We hope this review contributes to accelerating the utilization of the diagnostic, prognostic, and therapeutic potential of DNA methylation for the benefit of melanoma patients.
异常DNA甲基化是黑色素瘤的一种表观遗传特征,已知其在黑色素瘤的形成和进展中发挥重要作用。全基因组甲基化方法的最新进展为识别差异甲基化基因、甲基化特征和潜在生物标志物提供了手段。然而,尽管在对黑色素瘤中的甲基化变化进行编目方面付出了巨大努力并取得了进展,但许多问题仍未得到解答。本综述的目的是总结黑色素瘤异常DNA甲基化领域的最新进展、新趋势和重要的未解决问题。除了回顾最新进展外,我们还仔细综合研究结果,努力提供一个框架,以理解该领域的现状和发展方向。为便于阐述清晰,我们将综述分为黑色素瘤中的DNA甲基化变化、生物标志物机遇和治疗进展。我们希望本综述有助于加速利用DNA甲基化的诊断、预后和治疗潜力,造福黑色素瘤患者。