Department of Pediatrics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China.
Guangdong Provincial Key Laboratory of Malignant Tumour Epigenetics and Gene Regulation, Guangzhou, People's Republic of China.
Cancer Control. 2023 Jan-Dec;30:10732748231182787. doi: 10.1177/10732748231182787.
Zinc finger protein 384 () encodes a C2H2-type zinc finger protein that can function as a transcription factor. ZNF384 rearrangement in acute lymphoblastic leukemia (ALL) was first reported in 2002. More than 19 different ZNF384 fusion partners have been detected in ALL. These include E1A-binding protein P300 (), CREB-binding protein (), transcription factor 3 (), TATA-box binding protein associated factor 15 (), Ewing sarcoma breakpoint region 1 gene (), AT-rich interactive domain-containing protein 1B (), SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 4 (), SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2 (), synergin gamma (), clathrin heavy chain (), bone morphogenic protein 2-inducible kinase (), Nipped-B-like protein (), A Kinase Anchoring Protein 8 (), Chromosome 11 Open Reading Frame 74 (), DEAD-Box Helicase 42 (), ATP Synthase F1 Subunit Gamma (), Euchromatic Histone Lysine Methyltransferase 1 (), Testic Expressed 41 (), etc. Patients diagnosed with ALL harboring ZNF384 rearrangements commonly had a good prognosis. The mechanisms, performance, and features of different ZNF384 rearrangements in acute lymphoblastic leukemia have been well evaluated.
锌指蛋白 384() 编码一种 C2H2 型锌指蛋白,可作为转录因子发挥作用。2002 年首次报道急性淋巴细胞白血病 (ALL) 中的锌指蛋白 384 重排。在 ALL 中已经检测到超过 19 种不同的 ZNF384 融合伙伴。这些包括 E1A 结合蛋白 P300()、CREB 结合蛋白()、转录因子 3()、TATA 框结合蛋白相关因子 15()、尤文肉瘤断点区域 1 基因()、富含 AT 的相互作用域蛋白 1B()、SWI/SNF 相关、基质相关、肌动蛋白依赖性染色质调节剂亚家族 A 成员 4()、SWI/SNF 相关、基质相关、肌动蛋白依赖性染色质调节剂亚家族 A 成员 2()、协同蛋白 gamma()、网格蛋白重链()、骨形态发生蛋白 2 诱导激酶()、Nipped-B 样蛋白()、A 激酶锚定蛋白 8()、染色体 11 开放阅读框 74()、DEAD 框解旋酶 42()、ATP 合酶 F1 亚基 Gamma()、常染色质组蛋白赖氨酸甲基转移酶 1()、睾丸表达 41()等。诊断为 ALL 并伴有 ZNF384 重排的患者通常预后良好。不同 ZNF384 重排在急性淋巴细胞白血病中的机制、性能和特征已经得到了很好的评估。