Roman-Gomez Jose, Castillejo Juan A, Jimenez Antonio, Barrios Manuel, Heiniger Anabel, Torres Antonio
Department of Hematology, Reina Sofia Hospital, 14004 Cordoba, Spain.
Leuk Lymphoma. 2003 Nov;44(11):1855-64. doi: 10.1080/1042819031000116689.
The hallmark of acute lymphoblastic leukemia (ALL) is a progressive appearance of malignant cell behavior that is triggered by the evolution of altered gene function. ALL has traditionally been viewed as a genetic disease, however, epigenetic defects also play an important role. DNA promoter methylation has gained increasing recognition as an important mechanism for transcriptional silencing of cancer related genes. The hypermethylation-associated inactivation affects virtually all of the pathways in the ALL cellular network, such as the cell cycle, apoptosis and adhesion. The identification of these methylation abnormalities and elucidation of the mechanistic events surrounding them are of prime importance, as the methylation status of ALL cells can be used as prognostic biomarker and also can be manipulated in vivo with demethylating agents.
急性淋巴细胞白血病(ALL)的标志是恶性细胞行为的逐渐显现,这是由基因功能改变的演变引发的。传统上,ALL被视为一种遗传性疾病,然而,表观遗传缺陷也起着重要作用。DNA启动子甲基化作为癌症相关基因转录沉默的重要机制,越来越受到认可。与高甲基化相关的失活几乎影响了ALL细胞网络中的所有途径,如细胞周期、凋亡和黏附。识别这些甲基化异常并阐明其周围的机制事件至关重要,因为ALL细胞的甲基化状态可作为预后生物标志物,并且在体内可用去甲基化剂进行调控。