Nawrath M, Pavlovic J, Moelling K
Institute of Medical Virology, University of Zurich, Switzerland.
Cancer Gene Ther. 2000 Jun;7(6):963-72. doi: 10.1038/sj.cgt.7700207.
In many hematopoietic malignancies, c-Myb, a nuclear transcription factor of hematopoietic cells, is an activated oncogene. To achieve a specific inhibition of hematopoietic tumor growth, an inducible fusion protein consisting of the Myb DNA binding domain (DBD) and the active repressor domain KRAB, the Krüppel-associated box of the developmental zinc-finger protein KOX-1, was generated. The MybDBD-KRAB fusion protein is a potent repressor of Myb-induced gene expression from Myb-responsive reporter genes containing several Myb binding sites. MybDBD-KRAB expressed in the human hematopoietic promyelocytic cell line HL60 significantly reduces cell proliferation by inducing apoptosis. Expression of MybDBD-KRAB in subcutaneously injected HL60 cells leads to inhibition of tumor formation in nude mice. The MybDBD-KRAB effect is specific to cell lines expressing c-Myb. It is conceivable to fuse the KRAB domain to other DBDs of oncogenic transcription factors and target them to their respective DNA response elements to selectively drive tumor cells into apoptosis.
在许多造血系统恶性肿瘤中,c-Myb作为造血细胞的一种核转录因子,是一种激活的致癌基因。为了实现对造血肿瘤生长的特异性抑制,人们构建了一种可诱导的融合蛋白,它由Myb DNA结合结构域(DBD)和活性阻遏结构域KRAB(发育性锌指蛋白KOX-1的Krüppel相关框)组成。MybDBD-KRAB融合蛋白是一种有效的阻遏物,可抑制来自含有多个Myb结合位点的Myb反应性报告基因的Myb诱导基因表达。在人造血早幼粒细胞系HL60中表达的MybDBD-KRAB通过诱导凋亡显著降低细胞增殖。在皮下注射的HL60细胞中表达MybDBD-KRAB可导致裸鼠肿瘤形成受到抑制。MybDBD-KRAB的作用对表达c-Myb的细胞系具有特异性。可以设想将KRAB结构域与致癌转录因子的其他DBD融合,并将它们靶向各自的DNA反应元件,以选择性地促使肿瘤细胞凋亡。