Superior antiproliferative effects mediated by interferon-alpha entrapped in liposomes against a newly established human lung cancer cell line.

D M Shin, I J Fidler, C D Bucana, D Fan, W K Hong, J J Killion
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Abstract

The purpose of this study was to characterize the antiproliferative activity of a recombinant interferon-alpha (IFN-alpha) against a newly established human adenocarcinoma cell line (DMS-4C) and to determine whether IFN-alpha entrapped in multilamellar liposomes had superior antitumor effects compared with free IFN-alpha. Treatment of DMS-4C cells with 100 U/ml of free IFN-alpha resulted in 34% cytostasis. IFN-alpha encapsulated in phosphatidylcholine/phosphatidylserine multilamellar vesicles produced growth inhibition of 67%, which was significantly greater than that produced by free IFN-alpha or by control liposomes containing only medium combined with free IFN-alpha. Moreover, kinetic analysis revealed that to produce significant cytolysis, free IFN-alpha had to be incubated with target cells for at least 24 h, whereas IFN-alpha encapsulated into liposomes required only 30 min of exposure.

脂质体中包裹的干扰素- α介导的对新建立的人肺癌细胞系的卓越抗增殖作用。
本研究的目的是表征重组干扰素- α (ifn - α)对新建立的人腺癌细胞系(DMS-4C)的抗增殖活性,并确定包裹在多层脂质体中的ifn - α是否比游离的ifn - α具有更好的抗肿瘤作用。用100 U/ml游离ifn - α处理DMS-4C细胞,细胞抑制率为34%。磷脂酰胆碱/磷脂酰丝氨酸多层囊泡中包裹的ifn - α的生长抑制率为67%,显著高于游离ifn - α或仅含培养基与游离ifn - α的对照脂质体。此外,动力学分析显示,为了产生显著的细胞溶解作用,游离的ifn - α必须与靶细胞一起培养至少24小时,而包裹在脂质体中的ifn - α只需要暴露30分钟。
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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