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诱导骨髓增生异常肿瘤中端粒功能障碍和表观遗传改变引起的染色体不稳定性。

Induction of Chromosomal Instability via Telomere Dysfunction and Epigenetic Alterations in Myeloid Neoplasia.

机构信息

Institute of Cell and Molecular Pathology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.

出版信息

Cancers (Basel). 2013 Jul 4;5(3):857-74. doi: 10.3390/cancers5030857.

Abstract

Chromosomal instability (CIN) is a characteristic feature of cancer. In this review, we concentrate on mechanisms leading to CIN in myeloid neoplasia, i.e., myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). The pathogenesis of myeloid neoplasia is complex and involves genetic and epigenetic alterations. Chromosome aberrations define specific subgroups and guide clinical decisions. Genomic instability may play an essential role in leukemogenesis by promoting the accumulation of genetic lesions responsible for clonal evolution. Indeed, disease progression is often driven by clonal evolution into complex karyotypes. Earlier studies have shown an association between telomere shortening and advanced MDS and underlined the important role of dysfunctional telomeres in the development of genetic instability and cancer. Several studies link chromosome rearrangements and aberrant DNA and histone methylation. Genes implicated in epigenetic control, like DNMT3A, ASXL1, EZH2 and TET2, have been discovered to be mutated in MDS. Moreover, gene-specific hypermethylation correlates highly significantly with the risk score according to the International Prognostic Scoring System. In AML, methylation profiling also revealed clustering dependent on the genetic status. Clearly, genetic instability and clonal evolution are driving forces for leukemic transformation. Understanding the mechanisms inducing CIN will be important for prevention and for novel approaches towards therapeutic interventions.

摘要

染色体不稳定性(CIN)是癌症的一个特征。在这篇综述中,我们专注于导致骨髓增生性肿瘤(即骨髓增生异常综合征[MDS]或急性髓系白血病[AML])中 CIN 的机制。髓性肿瘤的发病机制复杂,涉及遗传和表观遗传改变。染色体异常定义了特定的亚组,并指导临床决策。基因组不稳定性通过促进负责克隆进化的遗传损伤的积累,可能在白血病发生中发挥重要作用。事实上,疾病进展通常是由复杂核型的克隆进化驱动的。早期的研究表明,端粒缩短与晚期 MDS 之间存在关联,并强调了功能失调的端粒在遗传不稳定性和癌症发展中的重要作用。一些研究将染色体重排与异常的 DNA 和组蛋白甲基化联系起来。涉及表观遗传控制的基因,如 DNMT3A、ASXL1、EZH2 和 TET2,已被发现存在于 MDS 中发生突变。此外,基因特异性高甲基化与根据国际预后评分系统计算的风险评分高度相关。在 AML 中,甲基化分析也揭示了依赖于遗传状态的聚类。显然,遗传不稳定性和克隆进化是白血病转化的驱动力。了解诱导 CIN 的机制对于预防和针对治疗干预的新方法都很重要。

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