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MLL-ENL介导的白血病起始于淋巴样分化界面处

MLL-ENL-mediated leukemia initiation at the interface of lymphoid commitment.

作者信息

Ugale A, Säwén P, Dudenhöffer-Pfeifer M, Wahlestedt M, Norddahl G L, Bryder D

机构信息

Molecular Hematology, Institution for Laboratory Medicine, Lund University, Lund, Sweden.

出版信息

Oncogene. 2017 Jun 1;36(22):3207-3212. doi: 10.1038/onc.2016.470. Epub 2017 Jan 9.

Abstract

Translocations involving the mixed lineage leukemia-1 are recurrent events in acute leukemia and associate with lymphoid (ALL), myeloid (AML) or mixed lineage (MLL) subtypes. Despite an association with ALL in humans, murine MLL fusion models are persistently restricted to AML. We here explored this issue using an inducible mixed lineage leukemia-eleven nineteen leukemia (MLL-ENL) mouse model. Although multiple progenitor cell types with myeloid potential are potent AML leukemia-initiating cells, also the earliest lymphoid progenitors were capable of initiating AML. This ability to evoke a latent myeloid potential in the earliest lymphoid progenitors was lost upon further lymphoid commitment. At the same time, more downstream/committed lymphoid precursors also failed to initiate lymphoid leukemia. Co-expression of MLL-ENL with a constitutively active RAS allele, the most common co-mutation in MLL fusion leukemias, could influence on both disease latency and lineage assignment of developing leukemia in what appears to be a mutation-order-dependent manner. Finally, CEBPB-mediated transdifferentation of committed and otherwise leukemia-incompetent B-cell progenitors imbued these cells with leukemic competence for AML. Therefore, apart from providing detailed insight into the differential responsiveness of candidate target cells to a first-hit MLL fusion event, our data warrants caution to therapeutic approaches based on the concept of transdifferentiation.

摘要

涉及混合谱系白血病-1的易位是急性白血病中的复发性事件,与淋巴样(急性淋巴细胞白血病,ALL)、髓样(急性髓细胞白血病,AML)或混合谱系(MLL)亚型相关。尽管在人类中与ALL有关联,但小鼠MLL融合模型一直局限于AML。我们在此使用诱导性混合谱系白血病-11-19白血病(MLL-ENL)小鼠模型探讨了这个问题。虽然多种具有髓样潜能的祖细胞类型是有效的AML白血病起始细胞,但最早的淋巴样祖细胞也能够引发AML。在进一步向淋巴样分化后,最早的淋巴样祖细胞中诱发潜在髓样潜能的这种能力丧失。与此同时,更多下游/已分化的淋巴样前体细胞也无法引发淋巴样白血病。MLL-ENL与组成型活性RAS等位基因(MLL融合白血病中最常见的共突变)的共表达,似乎以突变顺序依赖的方式影响疾病潜伏期和正在发展的白血病的谱系归属。最后,CEBPB介导的已分化且原本无白血病能力的B细胞祖细胞的转分化赋予这些细胞AML白血病能力。因此,除了深入了解候选靶细胞对首次发生的MLL融合事件的不同反应性之外,我们的数据还警示基于转分化概念的治疗方法。

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