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低浓度地西他滨和 SAHA 的联合治疗可导致白血病细胞系而非正常外周血淋巴细胞死亡。

Combined treatment with low concentrations of decitabine and SAHA causes cell death in leukemic cell lines but not in normal peripheral blood lymphocytes.

机构信息

Institute of Hematology and Blood Transfusion, Prague, Czech Republic.

出版信息

Biomed Res Int. 2013;2013:659254. doi: 10.1155/2013/659254. Epub 2013 Aug 13.

Abstract

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.

摘要

表观遗传学治疗可逆转异常乙酰化或甲基化,从而有针对性地靶向肿瘤细胞并保护正常细胞。联合表观遗传学治疗可能进一步提高单药治疗的效果。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)联合作用对不同白血病细胞系与外周血淋巴细胞的影响。结果显示,与正常外周血淋巴细胞相比,联合用药在 p53 状态不同的白血病细胞系中可显著降低细胞活力,诱导大量 p21WAF1,形成活性氧并表现出凋亡特征,而对健康供体的正常外周血淋巴细胞则基本无作用。研究表明,p53 依赖性凋亡途径参与了 wtp53 CML-T1 白血病细胞系的反应,而在 p53 缺失的 HL-60 细胞系中则检测到活性氧对细胞活力下降的显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b74/3755446/43e31379fc1b/BMRI2013-659254.001.jpg

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