Hematology Department, Affiliated Hospital of Chengde Medical College, Chengde, Hebei Province, People's Republic of China.
Onco Targets Ther. 2013 Jun 18;6:733-40. doi: 10.2147/OTT.S46135. Print 2013.
The chimeric fusion protein, AML1-ETO, generated by translocation of t(8;21), abnormally recruits histone deacetylase (HDAC) to the promoters of AML1 target genes, resulting in transcriptional repression of the target genes and development of t(8;21) acute myeloid leukemia. Abnormal expression of cyclin-dependent kinase inhibitors, especially p21, is considered a possible mechanism of the arrested maturation and differentiation seen in leukemia cells. A new generation of HDAC inhibitors is becoming an increasing focus of attention for their ability to induce differentiation and apoptosis in tumor cells and to block the cell cycle. Our previous research had demonstrated that valproic acid induces G0/G1 arrest of Kasumi-1 cells in t(8;21) acute myeloid leukemia. In this study, we further confirmed that valproic acid inhibits the growth of Kasumi-1 cells in a murine xenograft tumor model, and that this occurs via upregulation of histone acetylation in the p21 promoter region, enhancement of p21 expression, suppression of phosphorylation of retinoblastoma protein, blocking of transcription activated by E2F, and induction of G0/G1 arrest.
融合蛋白 AML1-ETO 由 t(8;21) 易位产生,异常募集组蛋白去乙酰化酶 (HDAC) 到 AML1 靶基因的启动子,导致靶基因转录抑制和 t(8;21) 急性髓系白血病的发生。细胞周期蛋白依赖性激酶抑制剂(尤其是 p21)的异常表达被认为是白血病细胞中成熟和分化停滞的可能机制。新一代 HDAC 抑制剂因其能够诱导肿瘤细胞分化和凋亡以及阻断细胞周期而引起越来越多的关注。我们之前的研究表明,丙戊酸诱导 t(8;21) 急性髓系白血病的 Kasumi-1 细胞 G0/G1 期阻滞。在这项研究中,我们进一步证实丙戊酸通过上调 p21 启动子区域的组蛋白乙酰化、增强 p21 表达、抑制视网膜母细胞瘤蛋白磷酸化、阻断 E2F 激活的转录,诱导 G0/G1 期阻滞,抑制 Kasumi-1 细胞在小鼠异种移植肿瘤模型中的生长。