Josep Carreras Leukaemia Research Institute (IJC), Barcelona, Spain.
Faculty of Pharmacy, University of Barcelona, Barcelona, Spain.
Sci Rep. 2018 Sep 17;8(1):13883. doi: 10.1038/s41598-018-32306-4.
Myelodysplastic syndromes (MDS) and chronic myelomonocytic leukemia (CMML) are chronic myeloid clonal neoplasms. To date, the only potentially curative therapy for these disorders remains allogeneic hematopoietic progenitor cell transplantation (HCT), although patient eligibility is limited due to high morbimortality associated with this procedure coupled with advanced age of most patients. Dopamine receptors (DRs) and serotonin receptors type 1 (HTR1s) were identified as cancer stem cell therapeutic targets in acute myeloid leukemia. Given their close pathophysiologic relationship, expression of HTR1s and DRs was interrogated in MDS and CMML. Both receptors were differentially expressed in patient samples compared to healthy donors. Treatment with HTR1B antagonists reduced cell viability. HTR1 antagonists showed a synergistic cytotoxic effect with currently approved hypomethylating agents in AML cells. Our results suggest that HTR1B constitutes a novel therapeutic target for MDS and CMML. Due to its druggability, the clinical development of new regimens based on this target is promising.
骨髓增生异常综合征(MDS)和慢性粒单核细胞白血病(CMML)是慢性髓系克隆性肿瘤。迄今为止,这些疾病唯一潜在的治愈性治疗方法仍然是异基因造血祖细胞移植(HCT),尽管由于该手术相关的高发病率和死亡率以及大多数患者的高龄,患者的入选资格受到限制。多巴胺受体(DRs)和 5-羟色胺受体 1 型(HTR1s)被确定为急性髓系白血病的癌症干细胞治疗靶点。鉴于它们密切的病理生理关系,在 MDS 和 CMML 中检测了 HTR1s 和 DRs 的表达。与健康供体相比,两种受体在患者样本中的表达存在差异。HTR1B 拮抗剂的治疗降低了细胞活力。HTR1 拮抗剂在 AML 细胞中与目前批准的低甲基化剂具有协同细胞毒性作用。我们的研究结果表明,HTR1B 是 MDS 和 CMML 的一个新的治疗靶点。由于其可成药性,基于该靶点的新方案的临床开发具有广阔的前景。