Department of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan; Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Department of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan; Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Cancer Lett. 2022 Feb 1;526:273-283. doi: 10.1016/j.canlet.2021.11.032. Epub 2021 Dec 4.
ABL1 tyrosine kinase inhibitors (TKIs) dramatically improve the prognosis of chronic myeloid leukemia (CML), but 10-20% of patients achieve suboptimal responses with low TKIs sensitivity. Furthermore, residual leukemic stem cells (LSCs) are involved in the molecular relapse after TKIs discontinuation. Aberrant DNA hypermethylation contributes to low TKIs sensitivity and the persistence of LSCs in CML. DNMT1 is a key regulator of hematopoietic stem cells, suggesting that aberrant DNA hypermethylation targeting DNMT1 represents a potential therapeutic target for CML. We investigated the efficacy of OR-2100 (OR21), the first orally available single-compound prodrug of decitabine. OR21 exhibited anti-tumor effects as a monotherapy, and in combination therapy it increased TKI-induced apoptosis and induction of tumor suppressor genes including PTPN6 encoding SHP-1 in CML cells. OR21 in combination with imatinib significantly suppressed tumor growth in a xenotransplant model. OR21 and combination therapy decreased the abundance of LSCs and inhibited engraftment in a BCR-ABL1-transduced mouse model. These results demonstrate that targeting DNMT1 using OR21 exerts anti-tumor effects and impairs LSCs in CML. Therefore, combination treatment of TKIs and OR21 represents a promising treatment strategy in CML.
ABL1 酪氨酸激酶抑制剂 (TKI) 显著改善了慢性髓性白血病 (CML) 的预后,但仍有 10-20%的患者对 TKI 反应不佳,敏感性较低。此外,残留的白血病干细胞 (LSCs) 参与了 TKI 停药后的分子复发。异常的 DNA 高甲基化导致 TKI 敏感性降低和 CML 中 LSCs 的持续存在。DNMT1 是造血干细胞的关键调节因子,这表明针对 DNMT1 的异常 DNA 高甲基化是 CML 的一个潜在治疗靶点。我们研究了 OR-2100 (OR21) 的疗效,OR21 是首个可口服的去甲基化剂地西他滨的单一化合物前药。OR21 作为单一疗法具有抗肿瘤作用,与 TKI 联合治疗时,可增加 CML 细胞中 TKI 诱导的凋亡,并诱导肿瘤抑制基因的表达,包括编码 SHP-1 的 PTPN6。OR21 联合伊马替尼可显著抑制异种移植模型中的肿瘤生长。OR21 和联合治疗可减少 LSCs 的丰度,并抑制 BCR-ABL1 转导的小鼠模型中的植入。这些结果表明,使用 OR21 靶向 DNMT1 可发挥抗肿瘤作用,并损害 CML 中的 LSCs。因此,TKI 和 OR21 的联合治疗代表了 CML 的一种有前途的治疗策略。