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Recombinant human granulocyte colony-stimulating factor enhanced cytotoxicity of Ara-C in Ara-C-resistant leukemic cells from a patient with biphenotypic leukemia in cell kinetic quiescence.

作者信息

Higashigawa M, Komada Y, Washio N, Kuwabara H, Hori H, Ido M, Sakurai M

机构信息

Department of Pediatrics, Mie University School of Medicine, Japan.

出版信息

Leuk Res. 1992 Oct;16(10):1049-54. doi: 10.1016/0145-2126(92)90085-l.

DOI:10.1016/0145-2126(92)90085-l
PMID:1383642
Abstract

In vitro preincubation with recombinant granulocyte colony-stimulating factor(rhG-CSF, 100 ng/ml) enhanced the cytotoxicity of 1-beta-D-arabinofuranosylcytosine(Ara-C) in leukemic cells resistant to Ara-C from a patient with biphenotypic leukemia. Treatment of the cells with rhG-CSF resulted in a 17-fold increase in DNA synthesis, 4.6-fold increase in percentage of S-phase, and a two-fold increase in Ara-CTP formation. Maximal effect was observed at 72 h of incubation. Combination chemotherapy with rhG-CSF and Ara-C to the patient showed remarkable cytoreduction. These results indicate that recruitment of resistant leukemic cells in cell kinetic quiescence is inducible by rhG-CSF and that it is possible enhancement of the cytotoxicity to cell cycle-specific drugs such as Ara-C.

摘要

相似文献

1
Recombinant human granulocyte colony-stimulating factor enhanced cytotoxicity of Ara-C in Ara-C-resistant leukemic cells from a patient with biphenotypic leukemia in cell kinetic quiescence.
Leuk Res. 1992 Oct;16(10):1049-54. doi: 10.1016/0145-2126(92)90085-l.
2
Colony-stimulating factors (rhG-CSF, rhGM-CSF, rhIL-3, and BCGF) recruit myeloblastic and lymphoblastic leukemic cells and enhance the cytotoxic effects of cytosine-arabinoside.集落刺激因子(重组人粒细胞集落刺激因子、重组人粒细胞巨噬细胞集落刺激因子、重组人白细胞介素-3和B细胞生长因子)募集成髓细胞性和淋巴细胞性白血病细胞,并增强阿糖胞苷的细胞毒性作用。
Haematol Blood Transfus. 1990;33:747-62. doi: 10.1007/978-3-642-74643-7_137.
3
In vitro response of blasts to IL-3, GM-CSF, and G-CSF is different for individual AML patients: factors that stimulate leukemic clonogenic cells also enhance Ara-C cytotoxicity.原始细胞对白细胞介素-3、粒细胞-巨噬细胞集落刺激因子和粒细胞集落刺激因子的体外反应在个体急性髓系白血病患者中存在差异:刺激白血病克隆形成细胞的因素也会增强阿糖胞苷的细胞毒性。
Ann Hematol. 1994 May;68(5):225-32. doi: 10.1007/BF01737421.
4
Combination of granulocyte colony-stimulating factor and low-dose cytosine arabinoside further enhances myeloid differentiation in leukemia cells in vitro.粒细胞集落刺激因子与低剂量阿糖胞苷联合使用可进一步增强白血病细胞在体外的髓系分化。
Leuk Lymphoma. 2000 Sep;39(1-2):173-84. doi: 10.3109/10428190009053552.
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Recombinant GM-CSF modulates the metabolism of cytosine arabinoside in leukemic cells in bone marrow.重组粒细胞-巨噬细胞集落刺激因子调节骨髓白血病细胞中阿糖胞苷的代谢。
Leuk Res. 1993 Jul;17(7):585-92. doi: 10.1016/0145-2126(93)90089-4.
6
Effects of mast cell growth factor on Ara-C mediated acute myeloid leukemia cell killing.肥大细胞生长因子对阿糖胞苷介导的急性髓系白血病细胞杀伤作用的影响。
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Enhanced chemosensitivity of clonogenic blasts from patients with acute myeloid leukemia by G-CSF, IL-3 or GM-CSF stimulation.粒细胞集落刺激因子、白细胞介素-3或粒细胞-巨噬细胞集落刺激因子刺激可增强急性髓系白血病患者克隆源性母细胞的化学敏感性。
Leukemia. 1993 Aug;7(8):1191-8.
8
Effect of granulocyte colony-stimulating factor on chemotherapeutic activity of cytosine arabinoside in acute leukemic cell lines.粒细胞集落刺激因子对急性白血病细胞系中阿糖胞苷化疗活性的影响。
Int J Hematol. 2001 Feb;73(2):199-205. doi: 10.1007/BF02981938.
9
Granulocyte-macrophage colony-stimulating factor enhances the cytotoxic effects of cytosine arabinoside in acute myeloblastic leukemia and in the myeloid blast crisis phase of chronic myeloid leukemia.粒细胞巨噬细胞集落刺激因子增强阿糖胞苷对急性髓细胞白血病及慢性髓细胞白血病髓系原始细胞危象期的细胞毒性作用。
Leukemia. 1989 May;3(5):328-34.
10
Enhancement of cytosine arabinoside cytotoxicity by granulocyte/macrophage colony-stimulating factor and granulocyte colony-stimulating factor in a human myeloblastic leukemia cell line.粒细胞/巨噬细胞集落刺激因子和粒细胞集落刺激因子增强阿糖胞苷对人髓性白血病细胞系的细胞毒性作用
Jpn J Cancer Res. 1993 Apr;84(4):445-50. doi: 10.1111/j.1349-7006.1993.tb00156.x.

引用本文的文献

1
Effect of granulocyte colony-stimulating factor on chemotherapeutic activity of cytosine arabinoside in acute leukemic cell lines.粒细胞集落刺激因子对急性白血病细胞系中阿糖胞苷化疗活性的影响。
Int J Hematol. 2001 Feb;73(2):199-205. doi: 10.1007/BF02981938.