Induction of G2/M arrest and inhibition of c-myc and p53 transcription by WP631 in Jurkat T lymphocytes

被引:30
|
作者
Villamarín, S
Ferrer-Miralles, N
Mansilla, S
Priebe, W
Portugal, J
机构
[1] CSIC, Inst Biol Mol Barcelona, Dept Mol Biol & Cellular, Barcelona 08034, Spain
[2] Univ Texas, MD Anderson Canc Ctr, Dept Bioimmunotherapy, Houston, TX 77030 USA
关键词
DNA binding; G(2) phase; Jurkat cells; c-myc; p53; polyploidy;
D O I
10.1016/S0006-2952(02)00865-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
WP631, a new DNA-binding drug that bisintercalates into DNA with high affinity, seems to be highly cytotoxic against Jurkat T lymphocytes. The purpose of this study was to gain new insights into the mechanisms by which WP631 halts proliferation in this cell type. Treating Jurkat cells with nanomolar concentrations of WP631 produced G(2)/M arrest, inhibited the transcription of c-myc and p53 genes, and induced limited apoptosis during the duration of treatment. Suppression of c-myc and p53 expression, and time-dependent decline in c-Myc and p53 protein levels, was associated with growth arrest. A weak interdependence was also found between the potent antiproliferative activity and the apoptotic response; treatment with WP631 for 24-36 hr produced arrest in G(2)/M and allowed for partial DNA repair. Longer treatments with WP631 allowed some repaired cells to re-enter the cell cycle, but produced aneuploidy or apoptosis in others. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1251 / 1258
页数:8
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