粒细胞集落刺激因子及其受体表达对多种恶性细胞的影响。

The Korean Journal of Hematology Pub Date : 2012-09-01 Epub Date: 2012-09-25 DOI:10.5045/kjh.2012.47.3.219
Hee Won Moon, Tae Young Kim, Bo Ra Oh, Sang Mee Hwang, Jiseok Kwon, Ja-Lok Ku, Dong Soon Lee
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引用次数: 7

摘要

背景:粒细胞集落刺激因子(G-CSF)在抗癌化疗中被广泛用于提高中性粒细胞计数。我们研究了G-CSF对几种白血病细胞系的影响,并筛选了G-CSF受体(G-CSFR)在各种恶性细胞中的表达。方法:我们通过流式细胞术检测了最常用的商业形式的G-CSF(糖基化lenograstim和非糖基化filgrastim)对各种白血病细胞系的影响。此外,我们还利用实时荧光定量PCR技术筛选了38个实体瘤细胞系中G-CSFR mRNA的表达。结果:G-CSF刺激了3种白血病细胞系的增殖(与对照组相比,处理细胞的增殖增加40-80%),并诱导AML1/ETO+白血病细胞分化。38个实体瘤细胞系中,有5个细胞系(肝母细胞瘤、2个乳腺癌、喉癌鳞状细胞癌和黑色素瘤细胞系)表达G-CSFR mRNA。结论:本研究结果表明,治疗性G-CSF可能会刺激表达G-CSFR的恶性细胞的增殖和分化,提示在使用G-CSF治疗前,可能有必要对原发肿瘤细胞中G-CSFR的表达进行预筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells.

Background: Granulocyte-colony stimulating factor (G-CSF) is extensively used to improve neutrophil count during anti-cancer chemotherapy. We investigated the effects of G-CSF on several leukemic cell lines and screened for the expression of the G-CSF receptor (G-CSFR) in various malignant cells.

Methods: We examined the effects of the most commonly used commercial forms of G-CSF (glycosylated lenograstim and nonglycosylated filgrastim) on various leukemic cell lines by flow cytometry. Moreover, we screened for the expression of G-CSFR mRNA in 38 solid tumor cell lines by using real-time PCR.

Results: G-CSF stimulated proliferation (40-80% increase in proliferation in treated cells as compared to that in control cells) in 3 leukemic cell lines and induced differentiation of AML1/ETO+ leukemic cells. Among the 38 solid tumor cell lines, 5 cell lines (hepatoblastoma, 2 breast carcinoma, squamous cell carcinoma of the larynx, and melanoma cell lines) showed G-CSFR mRNA expression.

Conclusion: The results of the present study show that therapeutic G-CSF might stimulate the proliferation and differentiation of malignant cells with G-CSFR expression, suggesting that prescreening for G-CSFR expression in primary tumor cells may be necessary before using G-CSF for treatment.

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