医学
表观遗传学
突变
造血
癌变
髓系白血病
骨髓增生异常综合症
髓样
体细胞
癌症研究
种系突变
调节器
白血病
癌症
癌症的体细胞进化
免疫学
遗传学
基因
内科学
生物
干细胞
骨髓
出处
期刊:PubMed
日期:2022-01-01
卷期号:63 (6): 561-572
标识
DOI:10.11406/rinketsu.63.561
摘要
Somatic mutations in the epigenetic regulator ASXL1 are considered a poor prognostic factor in myeloid malignancies, including myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). ASXL1 mutations coexist with other mutations in majority of patients, suggesting that its mutation alone is insufficient to cause cancer. ASXL1 mutations have been detected in age-related clonal hematopoiesis (CH), which has been linked to an increased risk of hematological malignancies. Therefore, ASXL1 mutations are likely to be one of the first events in the tumorigenesis process. With our most recent findings, we summarize the mechanisms by which ASXL1 mutations cause CH and hematological malignancies in this review.
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