Nitric oxide prevents γ-radiation-induced cell cycle arrest by impairing p53 function in MCF-7 cells

被引:16
作者
Chazotte-Aubert, L
Pluquet, O
Hainaut, P
Ohshima, H
机构
[1] Int Agcy Res Canc, Unit Endogenous Canc Risk Factors, F-69372 Lyon 08, France
[2] Int Agcy Res Canc, Grp Mol Carcinogenesis, F-69372 Lyon 08, France
关键词
apoptosis; Bax; cell cycle arrest; DNA binding; irradiation; MCF-7; cells; nitric oxide (NO); p53; p21(waf-1); S-nitrosoglutathione (GSNO);
D O I
10.1006/bbrc.2001.4423
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
We previously reported that nitric oxide (NO) released from S-nitrosoglutathione induces conformational change of the p53 tumor-suppressor protein that impairs its DNA-binding activity in vitro. We now demonstrate that MCF-7 cells preincubated in the presence of 0.5-1 mM S-nitrosoglutathione for 4 h before gamma -irradiation failed to arrest in the G1 phase of the cell cycle, whereas those gamma -irradiated without S-nitrosoglutathione exhibited a normal cell cycle arrest. The S-nitrosoglutathione-treated cells did not express the p53 target gene p21(waf-1) after gamma -irradiation, although p21(waf-1) was strongly expressed in cells irradiated in the absence of S-nitrosoglutathione. These results strongly suggest that NO impairs the function of p53 possibly via conformational change and/or amino acid modifications. On the other hand, cells incubated for 16 h in the presence of 1 mM S-nitrosoglutathione underwent apoptosis with accumulation of the pro-apoptotic protein Bax. This Bax accumulation, however, was shown to occur via a p53-independent pathway. (C) 2001 Academic Press.
引用
收藏
页码:766 / 771
页数:6
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