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[氯化锂和三尖杉酯碱对HL-60细胞分化、增殖及c-myc原癌基因表达的影响]

[Effects of lithium chloride and harringtonine on the differentiation, proliferation and c-myc proto-oncogene expression of HL-60 cells].

作者信息

Li W, Jiang D, Tan M

机构信息

Research Laboratory of Blood Physiology, Hunan Medcial University, Changsha.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 1997 May;13(2):151-3.

Abstract

This research was to observe the effects of lithium chloride (LiCl) and Harringtonine (HT) on the proliferation and differentiation of HL-60 leukemia cells. The results obtained by liquid suspension culture, semi-solid colony culture and 3H-TdR incorporation into HL-60 cells indicated that different concentrations of LiCl (5-20 mmol/L) and HT (10(-8)-10(-5)mol/L) exerted the inhibitory effects in a dose-dependent manner on HL-60 cell proliferation respectively. When LiCl (10 mmol/L) and HT (10(-7) mol/L) were added together in the liquid culture or semi-solid culture of HL-60 cells, they showed much greater inhibitory effect than that by each agent separately. It was discovered that there was induction of the differentiation of HL-60 cells by lithium and HT and the induction of HL-60 cells differentiation by HT was markedly enhanced by the addition of low concentration of lithium. This work also showed that by treating HL-60 cells with lithium and HT, the expression of the c-myc proto-oncogene was markedly decreased as measured by RT/PCR-mRNA (P < 0.01). These findings provide some evidence of the mechanismcausing leukemic change and of the potential use of lithium and HT in the treatment of leukemia and in vitro purging of leukemic cells for autologous bone marrow transplantation.

摘要

本研究旨在观察氯化锂(LiCl)和高三尖杉酯碱(HT)对HL-60白血病细胞增殖和分化的影响。通过液体悬浮培养、半固体集落培养以及3H-TdR掺入HL-60细胞所获得的结果表明,不同浓度的LiCl(5 - 20 mmol/L)和HT(10^(-8) - 10^(-5)mol/L)分别对HL-60细胞增殖具有剂量依赖性抑制作用。当在HL-60细胞的液体培养或半固体培养中同时加入LiCl(10 mmol/L)和HT(10^(-7) mol/L)时,它们显示出比单独使用每种药物更强的抑制作用。发现锂和HT可诱导HL-60细胞分化,并且加入低浓度锂可显著增强HT对HL-60细胞分化的诱导作用。本研究还表明,用锂和HT处理HL-60细胞后,通过RT/PCR-mRNA检测发现c-myc原癌基因的表达显著降低(P < 0.01)。这些发现为白血病发生机制以及锂和HT在白血病治疗和体外清除白血病细胞用于自体骨髓移植方面的潜在应用提供了一些证据。

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