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白血病发生:不止于突变基因。

Leukaemogenesis: more than mutant genes.

机构信息

Department of Medicine, University of Chicago, IL 60637, USA.

出版信息

Nat Rev Cancer. 2010 Jan;10(1):23-36. doi: 10.1038/nrc2765.

Abstract

Acute leukaemias are characterized by recurring chromosomal aberrations and gene mutations that are crucial to disease pathogenesis. It is now evident that epigenetic modifications, including DNA methylation and histone modifications, substantially contribute to the phenotype of leukaemia cells. An additional layer of epigenetic complexity is the pathogenetic role of microRNAs in leukaemias, and their key role in the transcriptional regulation of tumour suppressor genes and oncogenes. The genetic heterogeneity of acute leukaemias poses therapeutic challenges, but pharmacological agents that target components of the epigenetic machinery are promising as a component of the therapeutic arsenal for this group of diseases.

摘要

急性白血病的特征是反复出现的染色体异常和基因突变,这些对于疾病的发病机制至关重要。现在已经很明显,表观遗传修饰,包括 DNA 甲基化和组蛋白修饰,对白血病细胞的表型有很大的影响。表观遗传复杂性的另一个层次是 microRNAs 在白血病中的发病作用,以及它们在肿瘤抑制基因和癌基因的转录调控中的关键作用。急性白血病的遗传异质性带来了治疗上的挑战,但是靶向表观遗传机制成分的药物作为这组疾病治疗武器库的一部分,具有广阔的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d0/2972637/3ba34adf0a9a/nihms-246967-f0001.jpg

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