SR31747A is a sigma receptor ligand exhibiting antitumoural activity both in vitro and in vivo

被引:30
作者
Berthois, Y
Bourrié, B
Galiègue, S
Vidal, H
Carayon, P
Martin, PM
Casellas, P
机构
[1] Sanofi Synthelabo Rech, Dept Immunol Oncol, F-34184 Montpellier 04, France
[2] IFR Jean Roche, Lab Cancerol Expt, EA2671, Fac Med Secteur Nord, F-13916 Marseille, France
关键词
SR31747A; sigma receptors; human sterol isomerase; proliferation inhibition; breast and prostate cancer;
D O I
10.1038/sj.bjc.6600709
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
SR31747A is a recently described sigma receptor ligand that binds SR31747A-binding protein I (SR-BP) and emopamil-binding protein (EBP) (also called the sigma I receptor and the human sterol isomerase (HSI), respectively), and has immunoregulator and antiproliferative activities. To further investigate its antitumour activity and focusing on cancers, which are sensitive to the molecule, we measured the proliferation of different human epithelial breast or prostate cancer cell lines following in vitro and in vivo SR31747A treatment. Firstly, in vitro, we found that nanomolar concentrations of SR31747A dramatically inhibited cell proliferation in both hormono-responsive and -unresponsive cancer cell lines. Secondly, tumour development was significantly decreased in mice treated with SR31747A. In an attempt to decipher the SR31747A mode of action, we found that the two binding sites may not fully account for this activity. Indeed, while competitive experiments indicated that EBP prevails in mediating SR31747A anti proliferative activity, an analysis of the expression of both receptors indicated that the cellular sensitivity to SR31747A is not correlated with either EBP or SR-BP expression. These data suggest that additional binding sites may exist. Preliminary binding studies demonstrated that SR31747A also binds to sigma2, a protein that has not yet been cloned, but which is considered as a potential marker of the proliferative status of tumour cells. Altogether, our data demonstrate the antitumoural activity of SR31747A both in vitro and in vivo in two different cancer models, broaden the spectrum of its binding proteins and enhance the potential for further therapeutic development of the molecule. (C) 2003 Cancer Research UK.
引用
收藏
页码:438 / 446
页数:9
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