首页> 外文期刊>BioMed research international >Combined Treatment with Low Concentrations of Decitabine and SAHA Causes Cell Death in Leukemic Cell Lines but Not in Normal Peripheral Blood Lymphocytes
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Combined Treatment with Low Concentrations of Decitabine and SAHA Causes Cell Death in Leukemic Cell Lines but Not in Normal Peripheral Blood Lymphocytes

机译:低浓度地卡他滨和SAHA的联合治疗可导致白血病细胞系中细胞死亡,但不会导致正常外周血淋巴细胞死亡

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摘要

Epigenetic therapy reverting aberrant acetylation or methylation offers the possibility to target preferentially tumor cells and to preserve normal cells. Combination epigenetic therapy may further improve the effect of individual drugs. We investigated combined action of demethylating agent decitabine and histone deacetylase inhibitor SAHA (Vorinostat) on different leukemic cell lines in comparison with peripheral blood lymphocytes. Large decrease of viability, as well as huge p21WAF1 induction, reactive oxygen species formation, and apoptotic features due to combined decitabine and SAHA action were detected in leukemic cell lines irrespective of their p53 status, while essentially no effect was observed in response to the combined drug action in normal peripheral blood lymphocytes of healthy donors. p53-dependent apoptotic pathway was demonstrated to participate in the wtp53 CML-T1 leukemic cell line response, while significant influence of reactive oxygen species on viability decrease has been detected in p53-null HL-60 cell line.
机译:逆转异常乙酰化或甲基化的表观遗传疗法提供了优先靶向肿瘤细胞并保存正常细胞的可能性。表观遗传学治疗可以进一步提高单个药物的疗效。我们研究了去甲基化剂地西他滨和组蛋白去乙酰化酶抑制剂SAHA(伏立诺他)与外周血淋巴细胞相比在不同白血病细胞系上的联合作用。在白血病细胞系中,无论它们的p53状态如何,都检测到由于地西他滨和SAHA联合作用而导致的活力大幅下降,以及巨大的p21WAF1诱导,活性氧形成和凋亡特征,而对联合反应未观察到作用健康捐献者正常外周血淋巴细胞中的药物作用。已证明p53依赖的凋亡途径参与wtp53 CML-T1白血病细胞系反应,而在p53无效的HL-60细胞系中已检测到活性氧对活力降低的显着影响。

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