染色体易位
淋巴细胞白血病
癌症研究
Blinatumoab公司
临床意义
B细胞
基因
生物
医学
抗体
肿瘤科
免疫学
遗传学
内科学
白血病
作者
Wendy Su,Alair Zhao,Jonah Nahoul,Hailey Mendelsohn,Bilal Hamid,Carlos A Tirado
出处
期刊:PubMed
日期:2022-01-01
卷期号:48 (3): 100-105
摘要
B-cell acute lymphoblastic leukemia (B-ALL) is a subset of ALL that comprises 75% of ALL cases. There are a variety of chromosome aneuploidy or chromosomal rearrangements implicated in B-ALL. Deregulation of CRLF2 expression is seen in 5-15% of B-ALL patients and occurs primarily via a reciprocal translocation with immunoglobulin heavy chain (IGH), rearrangements of CRLF2, deletion within the PAR1 region of the X and Y chromosomes, and CRLF2 mutations as well as mutations of the CRLF2-involved pathways and are seen in Ph-like B-ALL. They are associated with a poor prognosis. Blinatumomab is an available immunotherapy, and there are currently a few ongoing clinical trials to treat CRLF2 B-ALL. This review focuses on the role of CRLF2 in B-ALL and summarizes the literature regarding its molecular pathways, clinical significance, incidence rates across demographics, therapies, and areas of further research.
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