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Effects of carboplatin in combination with other anticancer agents on human leukemia cell lines.
Leuk Res. 1993 Feb;17(2):113-9. doi: 10.1016/0145-2126(93)90055-p.
2
Combinations of interferon with platinum complexes: synergistic and antagonistic effects on growth inhibition of MCF-7 and MDA-MB231 breast cancer cells.干扰素与铂配合物的组合:对MCF-7和MDA-MB231乳腺癌细胞生长抑制的协同和拮抗作用。
J Cancer Res Clin Oncol. 1994;120(5):286-92. doi: 10.1007/BF01236385.
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Interactions of human leukocyte interferon with vinca alkaloids and other chemotherapeutic agents against human tumors in clonogenic assay.人白细胞干扰素与长春花生物碱及其他化疗药物在克隆形成试验中对人肿瘤的相互作用。
Cancer Chemother Pharmacol. 1983;10(3):161-6. doi: 10.1007/BF00255753.
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Effects of cloned human leukocyte interferons in the human tumor stem cell assay.克隆化人白细胞干扰素在人肿瘤干细胞试验中的作用
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Combined recombinant human interferon alpha 2 and cytotoxic agents studied in a clonogenic assay.在克隆形成试验中研究重组人干扰素α 2与细胞毒性药物的联合作用。
Int J Cancer. 1985 Jun 15;35(6):721-9. doi: 10.1002/ijc.2910350605.
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Phase II trial of carboplatin in advanced malignant melanoma.卡铂用于晚期恶性黑色素瘤的II期试验。
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What is synergy?什么是协同作用?
Pharmacol Rev. 1989 Jun;41(2):93-141.
8
Synergistic antiproliferative effect of interferon-beta in combination with bleomycin or neocarzinostatin on HeLa cells in culture: additive effect when combined with adriamycin or mitomycin C.β-干扰素与博来霉素或新制癌菌素联合应用对培养的HeLa细胞的协同抗增殖作用:与阿霉素或丝裂霉素C联合应用时的相加作用。
J Interferon Res. 1987 Aug;7(4):419-25. doi: 10.1089/jir.1987.7.419.
9
New colorimetric cytotoxicity assay for anticancer-drug screening.用于抗癌药物筛选的新型比色细胞毒性测定法。
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10
Antitumor activities of interferon alpha, beta, and gamma and their combinations on human melanoma cells in vitro: changes of proliferation, melanin synthesis, and immunophenotype.α、β和γ干扰素及其组合对人黑色素瘤细胞的体外抗肿瘤活性:增殖、黑色素合成及免疫表型的变化
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干扰素β与卡铂在体外对SK-MEL 28人黑素瘤细胞生长抑制的协同相互作用。

Synergistic interactions between interferon beta and carboplatin on SK-MEL 28 human melanoma cell growth inhibition in vitro.

作者信息

Hübner B, Eckert K, Garbe C, Maurer H R

机构信息

Institut für Pharmazie, Freien Universität Berlin, Germany.

出版信息

J Cancer Res Clin Oncol. 1995;121(2):84-8. doi: 10.1007/BF01202218.

DOI:10.1007/BF01202218
PMID:7883780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12200573/
Abstract

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.

摘要

在体外对卡铂和β-干扰素(IFNβ)单独及联合使用时对人黑色素瘤细胞系SK-MEL 28的抗增殖活性进行了测试。细胞在卡铂(0.1 mM和0.1 μM)和β-干扰素(5 pM和5 nM)存在的情况下孵育4天,通过磺酰罗丹明B测定法确定细胞生长抑制情况。使用贝伦鲍姆超平面定理分析药物组合的抗增殖作用,以确定相加、协同和拮抗作用。基于IC50值(IFNβ:IC50 = 1.24 nM,卡铂:IC50 = 18.2 μM),发现IFNβ抑制SK-MEL 28细胞生长的活性比卡铂高10000倍。添加0.5 nM的IFNβ可使卡铂的IC50值降低18.0倍;添加0.05 nM的IFNβ时,测得剂量降低1.84倍。在卡铂与IFNβ的摩尔浓度比为2000:1和6000:1时,分别测定的相互作用指数(I)为0.66和0.83,表明两种药物之间存在协同相互作用。在更高的卡铂与IFNβ摩尔比(20000:1和60000:1)下,观察到相加相互作用(I = 1.07和1.20)。然而,需要对几种黑色素瘤细胞系进行进一步的体外研究,以评估卡铂和IFNβ药物组合最终临床应用的潜在有效性。