Li Bin E, Ernst Patricia
Department of Genetics, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Department of Genetics, Geisel School of Medicine at Dartmouth, Hanover, NH, USA; Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA; Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Hanover, NH, USA; Department of Pediatrics Hematology/Oncology/BMT, University of Colorado Anschutz Medical Center, Aurora, CO, USA.
Exp Hematol. 2014 Dec;42(12):995-1012. doi: 10.1016/j.exphem.2014.09.006. Epub 2014 Sep 28.
MLL1, located on human chromosome 11, is disrupted in distinct recurrent chromosomal translocations in several leukemia subsets. Studying the MLL1 gene and its oncogenic variants has provided a paradigm for understanding cancer initiation and maintenance through aberrant epigenetic gene regulation. Here we review the historical development of model systems to recapitulate oncogenic MLL1-rearrangement (MLL-r) alleles encoding mixed-lineage leukemia fusion proteins (MLL-FPs) or internal gene rearrangement products. These largely mouse and human cell/xenograft systems have been generated and used to understand how MLL-r alleles affect diverse pathways to result in a highly penetrant, drug-resistant leukemia. The particular features of the animal models influenced the conclusions of mechanisms of transformation. We discuss significant downstream enablers, inhibitors, effectors, and collaborators of MLL-r leukemia, including molecules that directly interact with MLL-FPs and endogenous mixed-lineage leukemia protein, direct target genes of MLL-FPs, and other pathways that have proven to be influential in supporting or suppressing the leukemogenic activity of MLL-FPs. The use of animal models has been complemented with patient sample, genome-wide analyses to delineate the important genomic and epigenomic changes that occur in distinct subsets of MLL-r leukemia. Collectively, these studies have resulted in rapid progress toward developing new strategies for targeting MLL-r leukemia and general cell-biological principles that may broadly inform targeting aberrant epigenetic regulators in other cancers.
MLL1位于人类11号染色体上,在几种白血病亚型中,其在不同的复发性染色体易位中被破坏。对MLL1基因及其致癌变体的研究为通过异常表观遗传基因调控来理解癌症的发生和维持提供了一个范例。在这里,我们回顾了模型系统的历史发展,以重现编码混合谱系白血病融合蛋白(MLL-FPs)或内部基因重排产物的致癌性MLL1重排(MLL-r)等位基因。这些主要是小鼠和人类细胞/异种移植系统,已被建立并用于了解MLL-r等位基因如何影响多种途径,从而导致高度侵袭性、耐药性白血病。动物模型的特定特征影响了转化机制的结论。我们讨论了MLL-r白血病的重要下游促成因素、抑制剂、效应器和协同因子,包括直接与MLL-FPs和内源性混合谱系白血病蛋白相互作用的分子、MLL-FPs的直接靶基因,以及已被证明对支持或抑制MLL-FPs的致白血病活性有影响的其他途径。动物模型的使用已通过患者样本、全基因组分析得到补充,以描绘在不同亚型的MLL-r白血病中发生的重要基因组和表观基因组变化。总的来说,这些研究在开发针对MLL-r白血病的新策略以及可能广泛指导针对其他癌症中异常表观遗传调节因子的一般细胞生物学原理方面取得了迅速进展。