化疗药物对人骨髓祖细胞和淋巴母细胞系克隆细胞的抑制作用

C.K.Oladipupo Williams , Takao Ohnuma, James F. Holland
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引用次数: 5

摘要

利用甲基纤维素为基础的半固体培养基,富集了完全α培养基和未透析的胎牛血清,比较了甲氨喋呤(MTX)、长春新碱(VCR)、氢化可的松(HC)和柔红霉素(DNR)对淋巴细胞白血病细胞系(MOLT-4)的克隆原细胞(CFU)和正常骨髓粒细胞祖细胞(CFU- c)的细胞毒性作用,以及MTX细胞毒性的白藜芦醇(LV)的可逆性。MTX、VCR和HC对肿瘤细胞的抑制作用在细胞短暂或持续暴露于药物后更为明显。DNR对两种细胞类型的抑制作用相同。为了逆转MTX对MOLT-4 CFU的抑制作用,LV浓度需要比MTX浓度至少高一个对数阶。当MTX浓度较高时,左室逆转效果较差。在实验条件下,四种不同的人骨髓中只有一种被MTX显著抑制。结果表明,高浓度核苷和脱氧核苷使MTX对正常人骨髓CFU- c的细胞毒性消失,而对MOLT-4 CFU的细胞毒性消失,而在VCR和HC中观察到的差异抑制是由于白血病细胞更敏感。
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Inhibition by chemotherapeutic agents of human bone marrow progenitor cells and clonogenic cells of a lymphoblastic cell line

Using methylcellulose based semi-solid medium enriched with complete alpha medium and undialysed fetal calf serum, we compared the cytotoxic effects between the clonogenic cell (CFU) of a lymphoblastic leukemia cell line (MOLT-4) and normal bone marrow granulocytic progenitor cells (CFU-C) of methotrexate (MTX), vincristine (VCR), hydrocortisone (HC) and daunorubicin (DNR), as well as the reversibility by leukovorin (LV) of MTX cytotoxicity. The neoplastic cells were more markedly inhibited by MTX, VCR and HC following either brief or continuous exposure of the cell to the drugs. Inhibition by DNR was identical for both cell types. In order to reverse the inhibitory effects of MTX in MOLT-4 CFU, LV concentrations needed were at least one log order higher than MTX concentrations. At higher concentrations of MTX, LV reversal was less effective. Only one of four different human bone marrows studied were significantly inhibited by MTX under the experimental conditions. It is suggested that the high concentrations of nucleosides and deoxynucleosides present in the medium aborted the MTX cytotoxicity on CFU-C of normal human marrow but not on MOLT-4 CFU, while the differential inhibition observed with VCR and HC was due to greater sensitivity of the leukemic cells.

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