IRF4公司
多发性骨髓瘤
转录因子
等离子体电池
癌症研究
生物
干扰素调节因子
免疫学
IRF8
基因
遗传学
作者
Alessandro Agnarelli,Tim Chevassut,Erika J. Mancini
标识
DOI:10.1016/j.leukres.2018.07.025
摘要
Multiple Myeloma (MM) is an incurable hematologic malignancy characterized by abnormal proliferation of plasma cells. Interferon Regulatory Factor 4 (IRF4), a member of the interferon regulatory family of transcription factors, is central to the genesis of MM. IRF4 is highly expressed in B cells and plasma cells where it plays essential roles in controlling B cell to plasma cell differentiation and immunoglobulin class switching. Overexpression of IRF4 is found in MM patients’ derived cells, often as a result of activating mutations or translocations, where it is required for their survival. In this review, we first describe the roles of IRF4 in B cells and plasma cells and then analyse the subversion of the IRF4 transcriptional network in MM. Moreover, we discuss current therapies for MM as well as direct targeting of IRF4 as a potential new therapeutic strategy.
科研通智能强力驱动
Strongly Powered by AbleSci AI