首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Synergistic interactions between interferon beta and carboplatin on SK-MEL 28 human melanoma cell growth inhibition in vitro.
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Synergistic interactions between interferon beta and carboplatin on SK-MEL 28 human melanoma cell growth inhibition in vitro.

机译:干扰素β与卡铂之间的协同相互作用对SK-MEL 28人黑素瘤细胞生长抑制体外体外。

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Carboplatin and interferon beta (IFN beta) were tested alone and in combination for their antiproliferative activity on the human melanoma cell line SK-MEL 28 in vitro. Cells were incubated for 4 days in the presence of carboplatin (0.1 mM and 0.1 microM) and interferon beta (5 pM and 5 nM) and cell growth inhibition was determined by the sulphorhodamin B assay. The antiproliferative effects of the drug combinations were analysed using Berenbaum's hyperplane theorem to determine additive, synergistic and antagonistic effects. IFN beta was found to be 10,000 times more active in inhibiting cell growth of SK-MEL 28 cells than carboplatin on the basis of IC50 values (IFN beta: IC50 = 1.24 nM, carboplatin: IC50 = 18.2 microM). The addition of IFN beta at 0.5 nM reduced the IC50 value of carboplatin 18.0-fold; with IFN beta at 0.05 nM a dose reduction of 1.84 was measured. At the carboplatin: IFN beta molar concentration ratios of 2000:1 and 6000:1, interaction indices (I) of 0.66 and 0.83 were determined respectively, indicating synergistic interactions between the two drugs. At higher carboplatin: IFN beta molar ratios (20,000:1 and 60,000:1) an additive interaction was observed (I = 1.07 and 1.20). However, further in vitro studies with several melanoma cell lines are necessary to evaluate the potential effectiveness of the drug combination of carboplatin and IFN beta for eventual clinical utilisation.
机译:单独测试Carboplatin和干扰素β(IFNβ),并组合其对体黑色素瘤细胞系SK-MEL的抗增殖活性在体外。将细胞在卡铂(0.1mm和0.1 microm)存在下孵育4天,并且通过硫磺酰胺B测定法测定干扰素β(5mm和5nm)和细胞生长抑制。使用Berenbaum的血压定理分析药物组合的抗增殖效应来确定添加剂,协同和拮抗作用。如果基于IC 50值(IFNβ:IC50 = 1.24nm,Carboplatin:IC50 = 18.2 microm),IFNβ被发现在抑制SK-MEL 28细胞的细胞生长时抑制SK-MEL 28细胞的细胞生长至10,000倍。在0.5nm下添加IFNβ降低了18.0倍的Carboplatin的IC 50值;使用IFNβ,测量0.05nm的剂量降低1.84。在卡铂:2000:1和6000:1的IFNβ泡型浓度比,分别测定0.66和0.83的相互作用索引(I),表明两种药物之间的协同相互作用。在更高的卡铂:IFNβ泡醇比(20,000:1和60,000:1)观察到添加剂相互作用(i = 1.07和1.20)。然而,进一步的具有几种黑素瘤细胞系的体外研究是评估卡铂和IFNβ的药物组合对最终临床利用的潜在有效性。

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