Medizinische Klinik II, Abteilung für Hämatologie und Onkologie der, Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.
Invest New Drugs. 2010 Dec;28 Suppl 1(Suppl 1):S36-49. doi: 10.1007/s10637-010-9595-z. Epub 2010 Dec 14.
Imbalances of histone acetyltransferase (HAT) and deacetylase activity (DAC) that result in deregulated gene expression are commonly observed in leukemias. These alterations provide the basis for novel therapeutic approaches that target the epigenetic mechanisms implicated in leukemogenesis. As the acetylation status of histones has been linked to transcriptional regulation of genes involved particularly in differentiation and apoptosis, DAC inhibitors (DACi) have attracted considerable attention for treatment of hematologic malignancies. DACi encompass a structurally diverse family of compounds that are being explored as single agents as well as in combination with chemotherapeutic drugs, small molecule inhibitors of signaling pathways and hypomethylating agents. While DACi have shown clear evidence of activity in acute myeloid leukemia, myelodysplastic syndromes and lymphoid malignancies, their precise role in treatment of these different entities remain to be elucidated. Successful development of these compounds as elements of novel targeted treatment strategies for leukemia will require that clinical studies be performed in conjunction with translational research including efforts to identify predictive biomarkers.
组蛋白乙酰转移酶 (HAT) 和去乙酰化酶活性 (DAC) 的失衡导致基因表达失调,在白血病中很常见。这些改变为靶向参与白血病发生的表观遗传机制的新型治疗方法提供了基础。由于组蛋白的乙酰化状态与涉及分化和凋亡的基因的转录调控有关,DAC 抑制剂 (DACi) 作为治疗血液恶性肿瘤的药物受到了广泛关注。DACi 包含一个结构多样的化合物家族,它们被作为单一药物以及与化疗药物、信号通路小分子抑制剂和低甲基化剂联合使用进行研究。虽然 DACi 在急性髓性白血病、骨髓增生异常综合征和淋巴恶性肿瘤中显示出明确的活性,但它们在治疗这些不同实体中的确切作用仍有待阐明。这些化合物作为新型靶向治疗策略的一部分成功开发用于白血病治疗,需要与包括识别预测生物标志物在内的转化研究一起进行临床研究。