IRF4公司
干扰素调节因子
转录因子
生物
淋巴细胞生成
癌症研究
抑制器
造血
免疫系统
癌基因
背景(考古学)
基因
免疫学
遗传学
干细胞
细胞周期
古生物学
作者
Stella Amanda,Tze King Tan,Shinsuke Iida,Takaomi Sanda
标识
DOI:10.1016/j.exphem.2022.07.300
摘要
Dysregulation of transcription factor genes represents a unique molecular etiology of hematological malignancies. A number of transcription factors that play a role in hematopoietic cell development, lymphocyte activation, or their maintenance have been identified as oncogenes or tumor suppressors. Many of them exert oncogenic abilities in a context-dependent manner by governing the key transcriptional program unique to each cell type. IRF4, a member of the interferon regulatory factor (IRF) family, acts as an essential regulator of the immune system and is a prime example of a stage-specific oncogene. The expression and oncogenicity of IRF4 are restricted to mature lymphoid neoplasms, while IRF4 potentially serves as a tumor suppressor in other cellular contexts. This is in marked contrast to its immediate downstream target, MYC, which can cause cancers in a variety of tissues. In this review article, we provide an overview of the roles of IRF4 in the development of the normal immune system and lymphoid neoplasms and discuss the potential mechanisms of lineage- and stage-specific oncogenicity of IRF4.
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