Trimarchi Michael P, Mouangsavanh Mary, Huang Tim Hui-Ming
Human Cancer Genetics Program, Department of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, Ohio 43210, USA.
Chin J Cancer. 2011 Nov;30(11):749-56. doi: 10.5732/cjc.011.10128.
Epigenetic mechanisms, including DNA methylation, are responsible for determining and maintaining cell fate, stably differentiating the various tissues in our bodies. Increasing evidence shows that DNA methylation plays a significant role in cancer, from the silencing of tumor suppressors to the activation of oncogenes and the promotion of metastasis. Recent studies also suggest a role for DNA methylation in drug resistance. This perspective article discusses how DNA methylation may contribute to the development of acquired endocrine resistance, with a focus on breast cancer. In addition, we discuss DNA methylome profiling and how recent developments in this field are shedding new light on the role of epigenetics in endocrine resistance. Hormone ablation is the therapy of choice for hormone-sensitive breast tumors, yet as many as 40% of patients inevitably relapse, and these hormone refractory tumors often have a poor prognosis. Epigenetic studies could provide DNA methylation biomarkers to predict and diagnose acquired resistance in response to treatment. Elucidation of epigenetic mechanisms may also lead to the development of new treatments that specifically target epigenetic abnormalities or vulnerabilities in cancer cells. Expectations must be tempered by the fact that epigenetic mechanisms of endocrine resistance remain poorly understood, and further study is required to better understand how altering epigenetic pathways with therapeutics can promote or inhibit endocrine resistance in different contexts. Going forward, DNA methylome profiling will become increasingly central to epigenetic research, heralding a network-based approach to epigenetics that promises to advance our understanding of the etiology of cancer in ways not previously possible.
表观遗传机制,包括DNA甲基化,负责决定和维持细胞命运,使我们身体中的各种组织稳定分化。越来越多的证据表明,DNA甲基化在癌症中起着重要作用,从肿瘤抑制基因的沉默到癌基因的激活以及转移的促进。最近的研究还表明DNA甲基化在耐药性中发挥作用。这篇观点文章讨论了DNA甲基化如何可能导致获得性内分泌耐药的发展,重点是乳腺癌。此外,我们还讨论了DNA甲基化组分析以及该领域的最新进展如何为表观遗传学在内分泌耐药中的作用带来新的启示。激素消融是激素敏感性乳腺肿瘤的首选治疗方法,但多达40%的患者不可避免地会复发,而且这些激素难治性肿瘤的预后往往很差。表观遗传学研究可以提供DNA甲基化生物标志物,以预测和诊断对治疗的获得性耐药。对表观遗传机制的阐明也可能导致开发新的治疗方法,专门针对癌细胞中的表观遗传异常或弱点。必须认识到,内分泌耐药的表观遗传机制仍知之甚少,需要进一步研究以更好地理解用治疗方法改变表观遗传途径如何在不同情况下促进或抑制内分泌耐药。展望未来,DNA甲基化组分析将在表观遗传学研究中变得越来越重要,预示着一种基于网络的表观遗传学方法,有望以前所未有的方式推进我们对癌症病因的理解。