NF-M trans-activates the human DNA topoisomerase II alpha promoter independently of c-Myb in HL-60 cells

被引:5
作者
Brandt, TL
Kroll, DJ
机构
[1] UNIV COLORADO,SCH PHARM,DEPT PHARMACEUT SCI,DENVER,CO 80262
[2] UNIV COLORADO,CTR CANC,DENVER,CO 80262
关键词
cancer chemotherapy; C/EBP beta family; c-Myb; DNA topoisomerases; HL-60; cells; transcriptional activation;
D O I
10.1016/S0145-2126(97)00040-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Identifying transcriptional regulators of DNA topoisomerase II alpha (topo II alpha) is essential to decipher the mechanisms underlying leukemia cell resistance to topo II-directed antitumor drugs. We have previously reported that the proto-oncogene transcription factor c-Myb transactivates the topo II alpha promoter in several hematopoietic cell lines. Currently, we investigate whether NF-M, a C/EBP beta family member, cooperates with c-Myb in activating topo II alpha transcription. Although NF-M is the most efficacious trans-activator of topo II alpha that we have examined (similar to 38-fold over basal), NF-M does not appear to be involved in the endogenous transcriptional regulation of topo II alpha. Interestingly, we report that the sodium butyrate-dependent induction of the topo II alpha promoter observed previously appears to be mediated by c-Myb, independent of NF-M. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:711 / 720
页数:10
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