Interleukin-2 inhibits proliferation of HPV-associated tumor cells and halts tumor growth in vivo

被引:8
作者
Casana, PH [1 ]
Hernandez, H [1 ]
Arana, MJ [1 ]
机构
[1] Ctr Genet Engn & Biotechnol, Havana, Cuba
关键词
human papillomavirus type-16; tumor growth inhibition; interleukin-2; receptor;
D O I
10.1016/S0006-291X(02)02715-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies have shown inhibition of cervical cancer cell growth by treatment with high concentrations of IL-2. In the present study, we evaluated the in vitro and in vivo effects of recombinant human IL-2 on HPV-associated tumor cells (3T3-16). Treatment of 3T3-16 cells with rhIL-2 for 72 h inhibited cell growth in a dose-dependent manner and this effect was evidenced at nanomolar concentrations. These tumor cells expressed mRNA for beta and gamma subunits of the IL-2 receptor, which are required for signal transduction. In experiments to explore the effect of IL-2 on the growth of the HPV-associated tumor, mice received rhIL-2 through different routes: (i) intraperitoneal; (ii) subcutaneous, at the tumor inoculation sited or (iii) subcutaneous, distant from the tumor inoculation site. An effective antitumor response was observed only in those animals that received IL-2 at the tumor site (P < 0.01). These results indicate the potential adequacy of therapeutic strategies based on local administration of rhIL-2 for cervical carcinoma, not only based on the ability of this cytokine to stimulate cellular-mediated immunity but also because of its direct effects on tumor cells. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:818 / 824
页数:7
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