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Anti-leukemic agent useful for inducing differentiation in myeloid leukemia cells

机译:抗白血病剂可用于诱导髓样白血病细胞分化

摘要

The present invention provides the compound Ormeloxifene [3, 4-trans-2,2-dimethyl-3-phenyl-4-p-(beta-pyrrolidinoethoxy) phenyl-7-methoxy chroman] as useful in inducing differentiation in wide range of myeloid leukemias including acute promyelocytic leukemia, acute myeloid leukemia and chronic myeloid leukemia where block in differentiation is common feature. Ormeloxifene induced differentiation that is marked by increase in differentiation marker proteins like C/EBPα and surface proteins such as cd11b and granulocyte colony stimulating factor receptor (GCSFr). Differentiated cells having neutrophil like morphology were observed when treated with 1.0 uM to 7.5 uM ORM which clearly indicates that ORM can induce differentiation in myeloid leukemia cells. At higher doses (5 uM to 7.5 uM) there is early onset of myeloid differentiation (24 to 48 h) with reduced no. of cells which is likely due to apoptotic effects of ORM at higher does. In contrary, lower doses (1 uM) induce differentiation after longer duration (6-15 days) with quite reduced apoptotic effect.
机译:本发明提供了化合物Ormeloxifene [3,4-反式-2,2-二甲基-3-苯基-4-对-(β-吡咯烷基乙氧基)苯基-7-甲氧基苯并吡喃]可用于诱导广泛的髓样分化。白血病包括急性早幼粒细胞性白血病,急性髓性白血病和慢性髓性白血病,其中分化受阻是常见特征。奥美昔芬诱导分化,其特征在于分化标志物蛋白(如C /EBPα)和表面蛋白(如cd11b和粒细胞集落刺激因子受体(GCSFr))的增加。当用1.0 uM至7.5 uM ORM处理时,观察到具有嗜中性粒细胞样形态的分化细胞,这清楚地表明ORM可以诱导髓样白血病细胞分化。在较高剂量(5 uM至7.5 uM)下,骨髓分化较早开始(24至48 h),而no减少。可能是由于ORM在较高剂量时具有凋亡作用。相反,较低的剂量(1 uM)在较长的持续时间(6-15天)后诱导分化,且凋亡作用大大降低。

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