Fisher Joseph B, McNulty Maureen, Burke Michael J, Crispino John D, Rao Sridhar
Blood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI, USA.
Division of Hematology/Oncology, Northwestern University, Chicago, IL, USA.
Trends Cancer. 2017 Apr;3(4):282-293. doi: 10.1016/j.trecan.2017.02.006.
Acute Myeloid Leukemia (AML) is a hematologic malignancy with a poor prognosis. Recent genome-wide sequencing studies have identified frequent mutations in genes encoding members of the cohesin complex. Mutations in cohesin contribute to myeloid malignancies by conferring enhanced self-renewal of hematopoietic stem and progenitor cells but the mechanisms behind this phenotype have not been fully elucidated. Of note, cohesin mutations are highly prevalent in acute megakaryocytic leukemia associated with Down syndrome (DS-AMKL), where they occur in over half of patients. Evidence suggests that cohesin mutations alter gene expression through changes in chromatin accessibility and/or aberrant targeting of epigenetic complexes. In this review we discuss the pathogenic mechanisms by which cohesin mutations contribute to myeloid malignancies.
急性髓系白血病(AML)是一种预后较差的血液系统恶性肿瘤。最近的全基因组测序研究已经确定了编码黏连蛋白复合体成员的基因中频繁发生的突变。黏连蛋白突变通过赋予造血干细胞和祖细胞增强的自我更新能力来促进髓系恶性肿瘤的发生,但这种表型背后的机制尚未完全阐明。值得注意的是,黏连蛋白突变在与唐氏综合征相关的急性巨核细胞白血病(DS-AMKL)中高度普遍,超过半数的患者会出现这种突变。有证据表明,黏连蛋白突变通过染色质可及性的改变和/或表观遗传复合体的异常靶向作用来改变基因表达。在这篇综述中,我们讨论了黏连蛋白突变导致髓系恶性肿瘤的致病机制。