| Literature DB >> 26971355 |
Xin Xu1, Kunkun Han2, Xiaowen Tang3, Yuanying Zeng1, Xu Lin1, Yun Zhao4, Zubin Zhang1, Biyin Cao1, Depei Wu3, Xinliang Mao5.
Abstract
RNF6 is a little-studied ring finger protein. In the present study, we found that RNF6 was overexpressed in various leukemia cells and that it accelerated leukemia cell proliferation, whereas knockdown of RNF6 delayed tumor growth in xenografts. To find out the mechanism of RNF6 overexpression in leukemia, we designed a series of truncated constructs of RNF6 regulatory regions in the luciferase reporter system. The results revealed that the region between -144 and -99 upstream of the RNF6 transcription start site was critical and that this region contained a PBX1 recognition element (PRE). PBX1 modulated RNF6 expression by binding to the specific PRE. When PRE was mutated, RNF6 transcription was completely abolished. Further studies showed that PBX1 collaborated with PREP1 but not MEIS1 to modulate RNF6 expression. Moreover, RNF6 expression could be suppressed by doxorubicin, a major anti-leukemia agent, via down-regulating PBX1. This study thus suggests that RNF6 overexpression in leukemia is under the direction of PBX1 and that the PBX1/RNF6 axis can be developed as a novel therapeutic target of leukemia.Entities:
Keywords: RNF6; leukemia; oncogene; pre-B-cell leukemia homeobox 1; promoter modulation; ring finger protein; small interfering RNA (siRNA); transcription factor; tumor cell biology
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Year: 2016 PMID: 26971355 PMCID: PMC4850299 DOI: 10.1074/jbc.M115.701979
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157