Department of Haematology, Christian Medical College, Vellore, India; and.
Institute for Infection and Immunity, St George's University of London, London, UK.
Blood Adv. 2022 Jan 25;6(2):652-663. doi: 10.1182/bloodadvances.2021005300.
Acquired genetic mutations can confer resistance to arsenic trioxide (ATO) in the treatment of acute promyelocytic leukemia (APL). However, such resistance-conferring mutations are rare and do not explain most disease recurrence seen in the clinic. We have generated stable ATO-resistant promyelocytic cell lines that are less sensitive to all-trans retinoic acid (ATRA) and the combination of ATO and ATRA compared with the sensitive cell line. Characterization of these resistant cell lines that were generated in-house showed significant differences in immunophenotype, drug transporter expression, anti-apoptotic protein dependence, and promyelocytic leukemia-retinoic acid receptor alpha (PML-RARA) mutation. Gene expression profiling revealed prominent dysregulation of the cellular metabolic pathways in these ATO-resistant APL cell lines. Glycolytic inhibition by 2-deoxyglucose (2-DG) was sufficient and comparable to the standard of care (ATO) in targeting the sensitive APL cell line. 2-DG was also effective in the in vivo transplantable APL mouse model; however, it did not affect the ATO-resistant cell lines. In contrast, the resistant cell lines were significantly affected by compounds targeting mitochondrial respiration when combined with ATO, irrespective of the ATO resistance-conferring genetic mutations or the pattern of their anti-apoptotic protein dependency. Our data demonstrate that combining mitocans with ATO can overcome ATO resistance. We also show that this combination has potential for treating non-M3 acute myeloid leukemia (AML) and relapsed APL. The translation of this approach in the clinic needs to be explored further.
获得性基因突变可导致三氧化二砷(ATO)在治疗急性早幼粒细胞白血病(APL)中的耐药性。然而,这种耐药性突变很少见,不能解释临床上所见的大多数疾病复发。我们已经生成了稳定的 ATO 耐药性早幼粒细胞细胞系,与敏感细胞系相比,这些细胞系对全反式维甲酸(ATRA)和 ATO 与 ATRA 的联合治疗的敏感性降低。对这些在内部生成的耐药细胞系的特征分析表明,其免疫表型、药物转运蛋白表达、抗凋亡蛋白依赖性和早幼粒细胞白血病-维甲酸受体α(PML-RARA)突变存在显著差异。基因表达谱分析显示,这些 ATO 耐药性 APL 细胞系中细胞代谢途径出现明显失调。葡萄糖酵解抑制剂 2-脱氧葡萄糖(2-DG)在靶向敏感 APL 细胞系方面与标准治疗(ATO)一样有效。2-DG 也在体内可移植 APL 小鼠模型中有效;然而,它对 ATO 耐药细胞系没有影响。相反,当与 ATO 联合使用时,靶向线粒体呼吸的化合物对耐药细胞系有显著影响,而与耐药性基因突变的存在或其抗凋亡蛋白依赖性模式无关。我们的数据表明,将米托蒽醌与 ATO 联合使用可以克服 ATO 耐药性。我们还表明,这种联合治疗具有治疗非 M3 急性髓系白血病(AML)和复发性 APL 的潜力。需要进一步探索这种方法在临床上的应用。