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粒细胞集落刺激因子和视黄酸在体外协同诱导急性早幼粒细胞白血病细胞向粒细胞分化。

Granulocyte-colony stimulating factor and retinoic acid cooperatively induce granulocyte differentiation of acute promyelocytic leukemia cells in vitro.

作者信息

Nakamaki T, Sakashita A, Sano M, Hino K, Suzuki K, Tomoyasu S, Tsuruoka N, Honma Y, Hozumi M

机构信息

Department of Hematology, Showa University School of Medicine, Tokyo.

出版信息

Jpn J Cancer Res. 1989 Nov;80(11):1077-82. doi: 10.1111/j.1349-7006.1989.tb02262.x.

Abstract

The interaction of granulocyte-colony stimulating factor (G-CSF) and retinoic acid (RA) in proliferation and differentiation of acute promyelocytic leukemia (APL) cells was examined. G-CSF stimulated proliferation of APL cells at concentrations of 0.1 to 50 ng/ml in a dose dependent manner. More than 10(-8) M RA induced granulocytic differentiation of APL cells. Although G-CSF induced lysozyme activities in APL cells, it alone did not induce terminal differentiation of APL cells. G-CSF significantly enhanced the RA-induced granulocytic differentiation of APL cells in vitro. Enhancement by G-CSF was not due to the prolongation of survival of RA-induced differentiated cells, but the differentiation-inducing effects of G-CSF might be evident only in the presence of RA. Since G-CSF has a potential to induce the granulocytic differentiation of myeloid leukemia cells, G-CSF in combination with RA may be applicable in differentiation induction therapy for some types of myeloid leukemia.

摘要

研究了粒细胞集落刺激因子(G-CSF)与视黄酸(RA)在急性早幼粒细胞白血病(APL)细胞增殖和分化中的相互作用。G-CSF在0.1至50 ng/ml浓度下以剂量依赖性方式刺激APL细胞增殖。超过10^(-8) M的RA诱导APL细胞向粒细胞分化。虽然G-CSF诱导APL细胞中的溶菌酶活性,但它单独不能诱导APL细胞的终末分化。G-CSF在体外显著增强了RA诱导的APL细胞向粒细胞分化。G-CSF的增强作用不是由于RA诱导的分化细胞存活时间延长,而是G-CSF的分化诱导作用可能仅在RA存在时才明显。由于G-CSF有诱导髓系白血病细胞向粒细胞分化的潜力,G-CSF与RA联合可能适用于某些类型髓系白血病的分化诱导治疗。

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本文引用的文献

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Autoinduction of differentiation in WEHI-3B leukemia cells.
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Proliferative effect of human granulocyte colony-stimulating factor on blast cells of acute promyelocytic leukemia.
Jpn J Cancer Res. 1988 Jul;79(7):843-9. doi: 10.1111/j.1349-7006.1988.tb00046.x.

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