PNP Therapeutics, Birmingham, Alabama (W.B.P.); and UDG Healthcare, Smartanalyst - Ashfield Division, New York, New York (J.V.T.)
J Pharmacol Exp Ther. 2021 Nov;379(3):211-222. doi: 10.1124/jpet.121.000758. Epub 2021 Sep 9.
DNA methyltransferase (DNMT) 1 is an enzyme that functions as a maintenance methyltransferase during DNA replication, and depletion of this enzyme from cells is considered to be a rational goal in DNA methylation-dependent disorders. Two DNMT1-depleting agents 5-aza-2'-deoxycytidine (aza-dCyd, decitabine) and 5-aza-cytidine (aza-Cyd, azacitidine) are currently used for the treatment of myelodysplastic syndromes and acute myeloid leukemia and have also been investigated for nononcology indications, such as sickle cell disease. However, these agents have several off-target activities leading to significant toxicities that limit dosing and duration of treatment. Development of more selective inhibitors of DNMT1 could therefore afford treatment of long durations at effective doses. We have discovered that 5-aza-4'-thio-2'-deoxycytidine (aza-T-dCyd) is as effective as aza-dCyd in depleting DNMT1 in mouse tumor models but with markedly low toxicity. In this review we describe the preclinical studies that led to the development of aza-T-dCyd as a superior DNMT1-depleting agent with respect to aza-dCyd and will describe its pharmacology, metabolism, and mechanism of action. In an effort to understand why aza-T-dCyd is a more selective DNMT1 depleting agent than aza-dCyd, we will also compare and contrast the activities of these two agents. SIGNIFICANCE STATEMENT: Aza-T-dCyd is a potent DNMT1-depleting agent. Although similar in structure to decitabine (aza-dCyd), its metabolism and mechanism of action is different than that of aza-dCyd, resulting in less off-target activity and less toxicity. The larger therapeutic index of aza-T-dCyd (DNMT1 depletion vs. toxicity) in mice suggests that it would be a better clinical candidate to selectively deplete DNMT1 from target cells and determine whether or not depletion of DNMT1 is an effective target for various diseases.
DNA 甲基转移酶 (DNMT) 1 是一种在 DNA 复制过程中起维持甲基转移酶作用的酶,因此耗尽细胞中的这种酶被认为是 DNA 甲基化依赖性疾病的合理目标。两种 DNMT1 耗竭剂 5-氮杂-2'-脱氧胞苷 (aza-dCyd,地西他滨) 和 5-氮杂胞苷 (aza-Cyd,阿扎胞苷) 目前用于治疗骨髓增生异常综合征和急性髓系白血病,也已在非肿瘤适应证中进行了研究,例如镰状细胞病。然而,这些药物具有几种非靶向活性,导致显著的毒性,限制了剂量和治疗持续时间。因此,开发更具选择性的 DNMT1 抑制剂可以提供有效的治疗剂量并延长治疗时间。我们发现,5-氮杂-4'-硫代-2'-脱氧胞苷 (aza-T-dCyd) 在耗尽小鼠肿瘤模型中的 DNMT1 方面与 aza-dCyd 一样有效,但毒性明显降低。在这篇综述中,我们描述了导致 aza-T-dCyd 作为优于 aza-dCyd 的 DNMT1 耗竭剂的临床前研究,并将描述其药理学、代谢和作用机制。为了了解为什么 aza-T-dCyd 是比 aza-dCyd 更具选择性的 DNMT1 耗竭剂,我们还将比较和对比这两种药物的活性。意义声明:aza-T-dCyd 是一种有效的 DNMT1 耗竭剂。尽管与地西他滨 (aza-dCyd) 在结构上相似,但它的代谢和作用机制与 aza-dCyd 不同,导致非靶向活性和毒性更小。aza-T-dCyd 在小鼠中的更大治疗指数 (DNMT1 耗竭与毒性) 表明,它将是一种更好的临床候选药物,可以选择性地从靶细胞中耗尽 DNMT1,并确定耗尽 DNMT1 是否是各种疾病的有效靶点。