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首页> 外文期刊>International journal of oncology >Enhancement of differentiation induction and upregulation of CCAAT/enhancer-binding proteins and PU.1 in NB4 cells treated with combination of ATRA and valproic acid
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Enhancement of differentiation induction and upregulation of CCAAT/enhancer-binding proteins and PU.1 in NB4 cells treated with combination of ATRA and valproic acid

机译:ATRA和丙戊酸联合治疗对NB4细胞分化诱导的诱导作用及CCAAT /增强子结合蛋白和PU.1的上调

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The effects of all-trans retinoic acid (ATRA) and valproic acid (VPA), alone and in combination, on the human acute promyelocytic leukemia (APL) cell line NB4 were investigated in view of differentiation induction and growth inhibition. After 48?h of treatment, not only ATRA but also VPA induced differentiation in NB4 cells, and their combination further augmented the differentiation activity. Furthermore, the upregulation of transcription factors including CCAAT/enhancer-binding proteins (CEBPα, β, ε) and PU.1, which are known to be critical factors for normal myelopoiesis, granulocytic maturation and being repressed in APL, concurred with the differentiation induction. A significant cell growth inhibition was observed after the treatment with VPA, which was further strengthened by the addition of ATRA. Given the importance of C/EBPs and PU.1 in myeloid development, these results, thus, suggest that restoration of the normal function of the myeloid cell transcriptional machinery is a major molecular mechanism underlying the differentiation induction in NB4. Therefore, these results may provide novel insights into a possible combinational therapeutic approach for APL patients.
机译:考虑到分化诱导和生长抑制,研究了全反式视黄酸(ATRA)和丙戊酸(VPA)单独或组合对人急性早幼粒细胞白血病(APL)细胞系NB4的影响。处理48小时后,不仅ATRA而且VPA诱导了NB4细胞的分化,并且它们的组合进一步增强了分化活性。此外,包括CCAAT /增强子结合蛋白(CEBPα,β,ε)和PU.1在内的转录因子的上调与分化诱导有关,它们被认为是正常骨髓生成​​,粒细胞成熟和被APL抑制的关键因素。 VPA处理后观察到明显的细胞生长抑制作用,通过添加ATRA进一步增强了抑制作用。考虑到C / EBPs和PU.1在骨髓发育中的重要性,因此,这些结果表明,髓细胞转录机制正常功能的恢复是NB4分化诱导的主要分子机制。因此,这些结果可能为APL患者可能的联合治疗方法提供新颖的见解。

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