Lamba Gurpreet, Zaidi Sayyed Kaleem, Luebbers Kimberly, Verschraegen Claire, Stein Gary S, Rosmarin Alan
Division of Hematology/Oncology, University of Vermont, Burlington, Vermont; Vermont Cancer Center, Burlington, Vermont.
J Cell Biochem. 2014 Oct;115(10):1669-72. doi: 10.1002/jcb.24853.
Acute myeloid leukemia (AML) is an aggressive hematologic cancer that is characterized by accumulation of immature myeloid cells in the blood and bone marrow. The malignant cells in AML have reduced capacity to mature fully, and often exhibit chromosomal abnormalities, defects in cell signaling, and abnormal cell cycle control. Genetic and epigenetic changes are implicated in the onset and progression of AML. While progress has been made in using genetic and epigenetic changes as prognostic features of AML, these findings have not yet been effectively translated into novel treatment strategies. Disappointingly, rates of recurrence in AML remain high and overall survival is poor. Research strategies should focus on developing a comprehensive landscape of genetic and epigenetic changes in individual patients with AML to expand the clinicians' therapeutic armamentarium and to individualize and optimize treatment.
急性髓系白血病(AML)是一种侵袭性血液系统癌症,其特征是血液和骨髓中不成熟髓系细胞的积累。AML中的恶性细胞完全成熟的能力降低,并且常常表现出染色体异常、细胞信号传导缺陷和异常的细胞周期控制。遗传和表观遗传变化与AML的发生和进展有关。虽然在将遗传和表观遗传变化用作AML的预后特征方面已经取得了进展,但这些发现尚未有效地转化为新的治疗策略。令人失望的是,AML的复发率仍然很高,总体生存率很差。研究策略应侧重于描绘AML个体患者遗传和表观遗传变化的全面图景,以扩大临床医生的治疗手段,并实现治疗的个体化和优化。