ANTISENSE OLIGONUCLEOTIDES TO HUMAN LIPOCORTIN-1 INHIBIT GLUCOCORTICOID-INDUCED INHIBITION OF A549 CELL-GROWTH AND EICOSANOID RELEASE

被引:32
作者
CROXTALL, JD
FLOWER, RJ
机构
[1] Department of Biochemical Pharmacology, The William Harvey Institute, The Medical College, London, EC1M 6BQ, Charterhouse Square
基金
英国惠康基金;
关键词
LUNG ADENOCARCINOMA; ANNEXIN; 1; NEUTRALIZING ANTIBODY; PROSTAGLANDIN E(2); PROTEIN SYNTHESIS;
D O I
10.1016/0006-2952(94)90458-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glucocorticoids actively inhibit the growth of A549 cells by suppressing the release of factors such as prostaglandin E(2) (PGE(2)) necessary for their proliferation. This effect if largely mediated through induction of the protein lipocortin-1. We now show that transient transfection of A549 cells with an antisense DNA oligonucleotide targeted to a region coding the unique N-terminal portion of human lipocortin-1 blocks the induction of lipocortin-1 protein following glucocorticoid treatment and completely reverses glucocorticoid-induced suppression of cell proliferation and PGE(2) release. A scrambled oligonucleotide was without effect. Continued culture of A549 cells in the presence of this oligonucleotide results in a sustained increase in cell proliferation and PGE(2) release. This study reinforces the importance of lipocortin-1 as a negative modulator of cell growth and eicosanoid generation in this system.
引用
收藏
页码:1729 / 1734
页数:6
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