Furukawa Yutaka, Sutheesophon Krittaya, Wada Taeko, Nishimura Miki, Saito Yasushi, Ishii Hideshi, Furukawa Yusuke
Division of Stem Cell Regulation, Center for Molecular Medicine, Jichi Medical School, 3311-1 Yakushiji, Minamikawachi-machi, Tochigi 329-0498, Japan.
Mol Cancer Res. 2005 Jun;3(6):325-34. doi: 10.1158/1541-7786.MCR-04-0105.
Apaf-1 is important for tumor suppression and drug resistance because it plays a central role in DNA damage-induced apoptosis. Inactivation of the Apaf-1 gene is implicated in disease progression and chemoresistance of some malignancies. In this study, we attempted to clarify the role of Apaf-1 in leukemogenesis. Apaf-1 mRNA levels were below the detection limit or very low in 5 of 20 human leukemia cell lines (25%) and 5 of 12 primary acute myeloblastic leukemia cells (42%). There were no gross structural abnormalities in the Apaf-1 gene in these samples. Expression of factors regulating Apaf-1 transcription, such as E2F-1, p53, and Sp-1, did not differ between Apaf-1-positive and Apaf-1-negative cells. Methylation of CpG in the region between +87 and +128 of the Apaf-1 gene was almost exclusively observed in Apaf-1-defective cell lines. Treatment of these cells with 5-aza-2'-deoxycytidine, a specific inhibitor of DNA methylation, restored the expression of Apaf-1. Furthermore, we showed that the region between +87 and +128 could act as a repressor element by recruiting corepressors such as methylated DNA-binding domain 2 and histone deacetylase 1 upon methylation. Overexpression of Dnmt1, a mammalian maintenance DNA methyltransferase, was associated with Apaf-1 gene methylation. DNAs from Dnmt1-overexpressing cells were more resistant to digestion with methylation-sensitive enzyme HpaII than those from cells with low Dnmt1 expression, suggesting that Dnmt1 mediates aberrant methylation of multiple genes. In conclusion, methylation silencing is a mechanism of the inactivation of Apaf-1 in acute leukemia, and Dnmt1 overexpression may underlie hypermethylation of the Apaf-1 gene.
凋亡蛋白酶激活因子-1(Apaf-1)对肿瘤抑制和耐药性很重要,因为它在DNA损伤诱导的细胞凋亡中起核心作用。Apaf-1基因的失活与某些恶性肿瘤的疾病进展和化疗耐药性有关。在本研究中,我们试图阐明Apaf-1在白血病发生中的作用。在20个人类白血病细胞系中的5个(25%)和12个原发性急性髓细胞白血病细胞中的5个(42%)中,Apaf-1 mRNA水平低于检测限或非常低。这些样本中Apaf-1基因没有明显的结构异常。调节Apaf-1转录的因子如E2F-1、p53和Sp-1的表达在Apaf-1阳性和Apaf-1阴性细胞之间没有差异。Apaf-1基因+87至+128区域的CpG甲基化几乎仅在Apaf-1缺陷细胞系中观察到。用DNA甲基化特异性抑制剂5-氮杂-2'-脱氧胞苷处理这些细胞可恢复Apaf-1的表达。此外,我们表明+87至+128区域在甲基化后可通过募集甲基化DNA结合结构域2和组蛋白去乙酰化酶1等共抑制因子而作为抑制元件发挥作用。哺乳动物维持性DNA甲基转移酶Dnmt1的过表达与Apaf-1基因甲基化有关。来自Dnmt1过表达细胞的DNA比来自Dnmt1低表达细胞的DNA对甲基化敏感酶HpaII的消化更具抗性,表明Dnmt1介导多个基因的异常甲基化。总之,甲基化沉默是急性白血病中Apaf-1失活的一种机制,Dnmt1过表达可能是Apaf-1基因高甲基化的基础。