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Myeloid Neoplasia: Effect of the nonpeptide thrombopoietin receptor agonist Eltrombopag on bone marrow cells from patients with acute myeloid leukemia and myelodysplastic syndrome

机译:髓样瘤形成:非肽血小板生成素受体激动剂Eltrombopag对急性髓样白血病和骨髓增生异常综合症患者骨髓细胞的影响

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摘要

Thrombocytopenia is a frequent symptom and clinical challenge in patients with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Eltrombopag is a small molecule thrombopoietin receptor agonist that might be a new option to treat thrombocytopenia in these diseases, provided that it does not stimulate malignant hematopoiesis. In this work, we studied the effects of Eltrombopag on proliferation, apoptosis, differentiation, colony formation, and malignant self-renewal of bone marrow mononuclear cells of patients with AML and MDS. Malignant bone marrow mononuclear cells did not show increased proliferation, or increased clonogenic capacity at concentrations of Eltrombopag ranging from 0.1 to 30 μg/mL. On the contrary, we observed a moderate, statistically nonsignificant (P = .18), decrease of numbers of malignant cells (mean, 56%; SD, 28%). Eltrombopag neither led to increased 5-bromo-2-deoxyuridine incorporation, decreased apoptosis, an increase of malignant self-renewal, nor enhanced in vivo engraftment in xenotransplantations. Furthermore, we found that Eltrombopag was capable of increasing megakaryocytic differentiation and formation of normal megakaryocytic colonies in patients with AML and MDS. These results provide a preclinical rationale for further testing of Eltrombopag for treatment of thrombocytopenia in AML and MDS.
机译:血小板减少症是骨髓增生异常综合症(MDS)和急性髓性白血病(AML)患者的常见症状和临床挑战。 Eltrombopag是一种小分子血小板生成素受体激动剂,如果不刺激恶性造血作用,可能是治疗这些疾病中血小板减少症的新选择。在这项工作中,我们研究了Eltrombopag对AML和MDS患者的骨髓单个核细胞增殖,凋亡,分化,集落形成和恶性自我更新的影响。在Eltrombopag浓度为0.1至30μg/ mL范围内,恶性骨髓单个核细胞未显示出增生或增生能力。相反,我们观察到恶性细胞数量有所减少(统计学上无统计学意义(P = .18))(平均值为56%;标准差为28%)。 Eltrombopag既不会导致5-溴-2-脱氧尿苷掺入增加,凋亡减少,恶性自我更新的增加,也不会增强异种移植的体内植入。此外,我们发现Eltrombopag能够增加AML和MDS患者的巨核细胞分化和正常巨核细胞集落的形成。这些结果为进一步检测Eltrombopag治疗AML和MDS中的血小板减少症提供了临床前依据。

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