Wajed S A, Laird P W, DeMeester T R
Department of Surgery, University of Southern California School of Medicine, Los Angeles, California 90033, USA.
Ann Surg. 2001 Jul;234(1):10-20. doi: 10.1097/00000658-200107000-00003.
To provide an introduction to the concept of DNA methylation and its function in normal cells, and to explain the possible mechanisms as to how abnormalities in this phenomenon can relate to carcinogenesis. The clinical implications with reference to common malignancies encountered in surgical practice are discussed.
Methylation of DNA is a heritable, enzyme-induced modification to DNA structure without alteration of the specific sequence of the base pairs responsible for encoding the genome. DNA methylation can both directly inhibit the expression of genes and also increase the probability that affected genes undergo a mutational event. Although DNA methylation plays an essential role in normal biologic processes, distinct and abnormal patterns of methylation are observed in cancers. In particular, there has been increased documentation that methylation of the promoter regions of several genes, including known tumor suppressor genes, results in the subsequent failure to express their functional proteins. Consequently, DNA methylation may represent an early and fundamental step in the pathway by which normal tissue undergoes neoplastic transformation. Further, an assessment of the methylation profiles within neoplastic tissues may provide key information in enhancing the diagnosis, predicting the clinical behavior, and designing specific treatment plans for individual patients.
Published literature from 1925 to 2000 contributing to an understanding of the purpose of DNA methylation and how pathology of this phenomenon could contribute to cancer are reviewed. Theories on these issues and the evidence that led to them are described. The present status of the subject in a clinical context is discussed.
Gene expression can be significantly modulated by alterations in DNA methylation patterns. Methylation within the promoter regions of tumor suppressor genes causes their silencing, and methylation within the gene itself can induce mutational events. These mechanisms may play a fundamental role in precipitating the development of a large and diverse number of human cancers.
DNA methylation is an important factor in the development of cancer. A greater understanding of the relationship between DNA methylation events at the molecular level and its interaction in the clinical context may provide the basis for future advances in the surgical and pharmacologic management of malignant diseases.
介绍DNA甲基化的概念及其在正常细胞中的功能,并解释这一现象异常与致癌作用相关的可能机制。讨论其在外科实践中常见恶性肿瘤方面的临床意义。
DNA甲基化是一种可遗传的、由酶诱导的DNA结构修饰,而不改变负责编码基因组的碱基对的特定序列。DNA甲基化既能直接抑制基因表达,也会增加受影响基因发生突变事件的概率。虽然DNA甲基化在正常生物学过程中起着至关重要的作用,但在癌症中可观察到明显且异常的甲基化模式。特别是,越来越多的文献表明,包括已知肿瘤抑制基因在内的几个基因的启动子区域甲基化,会导致随后无法表达其功能性蛋白质。因此,DNA甲基化可能代表正常组织发生肿瘤转化途径中的一个早期且基本的步骤。此外,对肿瘤组织内甲基化谱的评估可能为加强诊断、预测临床行为以及为个体患者设计特定治疗方案提供关键信息。
回顾1925年至2000年发表的有助于理解DNA甲基化目的以及该现象的病理学如何导致癌症的文献。描述关于这些问题的理论以及导致这些理论的证据。讨论该主题在临床背景下的现状。
DNA甲基化模式的改变可显著调节基因表达。肿瘤抑制基因启动子区域内的甲基化导致其沉默,而基因本身内的甲基化可诱导突变事件。这些机制可能在引发大量不同类型的人类癌症发展中起重要作用。
DNA甲基化是癌症发展中的一个重要因素。更深入了解分子水平上DNA甲基化事件之间的关系及其在临床背景中的相互作用,可能为恶性疾病的外科和药物治疗未来进展提供基础。