Izraeli Shai
Department of Paediatric Haemato-Oncology, Sackler Faculty of Medicine, Cancer Research Centre, Safra's Children's Hospital, Sheba Medical Centre, Tel-Aviv University, Tel-Hashomer, Ramat-Gan, Israel.
Br J Haematol. 2004 Jul;126(1):3-10. doi: 10.1111/j.1365-2141.2004.04986.x.
Leukaemia is characterized by the accumulation of malignant haematopoietic precursors. Recent studies have revealed that acquired alterations in genes that regulate normal haematopoiesis are frequently detected in leukaemia. The progression to leukaemia depends on additional mutations that promote the survival of developmentally arrested cells. This review describes three examples of this general paradigm of leukaemogenesis: RUNX1 abnormalities in acute leukaemias, GATA1 mutations in the leukaemias of Down syndrome, and SCL and LMO2 ectopic expression in T cell acute lymphoblastic leukaemia.
白血病的特征是恶性造血前体细胞的积累。最近的研究表明,在白血病中经常检测到调节正常造血的基因发生后天改变。白血病的进展取决于促进发育停滞细胞存活的其他突变。本综述描述了白血病发生这一普遍模式的三个例子:急性白血病中的RUNX1异常、唐氏综合征白血病中的GATA1突变,以及T细胞急性淋巴细胞白血病中的SCL和LMO2异位表达。