髓系白血病
运行x1
骨髓增生异常综合症
白血病
癌症研究
移植
髓样
造血
急性白血病
造血干细胞移植
癌症的体细胞进化
干细胞
医学
肿瘤科
免疫学
生物
内科学
骨髓
遗传学
癌症
作者
Linlin Wang,Chong Gao,Baoan Chen
出处
期刊:PubMed
日期:2011-02-01
卷期号:19 (1): 254-9
被引量:3
摘要
Myelodysplastic syndrome (MDS) is a clonal hematopoietic stem cell disorder characterized by ineffective hematopoiesis and a risk of transformation into acute leukemia. Approximately 30% of patients with MDS will progress and develop into acute myeloid leukemia (AML), especially in the patients with high-risk MDS, which can be named as secondary acute myeloid leukemia (sAML or MDS/AML). Generally, chemotherapy for sAML hardly has any efficacy. The only way to cure the patients with sAML is allogeneic hematopoietic stem cell transplantation, but unfortunately, only few patients are appropriate for transplantation. So it is important to study the mechanisms of progression of MDS to AML and to explore the potent drug for clinical use. This review summarizes the mechanism of MDS transformation into AML from chromosomal abnormality, aberrant DNA methylation and gene mutation, such as AML1/RUNX1 mutations, FLT3 mutations and PI-PLCβ1 mono-allelic deletion.
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