Inhibition of phospholipid signalling and proliferation of Swiss 3T3 cells by the wortmannin analogue demethoxyviridin

被引:4
作者
Cross, MJ
Hodgkin, MN
Plumb, JA
Brunton, VG
Stewart, A
MacAully, G
Hill, R
Kerr, DJ
Workman, P
Wakelam, MJO [1 ]
机构
[1] Univ Birmingham, Sch Med, Inst Canc Studies, Birmingham B15 2TH, W Midlands, England
[2] Univ Glasgow, CRC, Dept Med Oncol, Glasgow G12 8QQ, Lanark, Scotland
[3] Univ Glasgow, Dept Organ Chem, Glasgow G12 8QQ, Lanark, Scotland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1997年 / 1362卷 / 01期
基金
英国惠康基金;
关键词
wortmannin; demethoxyviridin; signal-transduction; cell-proliferation; phospholipases;
D O I
10.1016/S0925-4439(97)00053-7
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
Growth factors and certain oncogenes activate a range of phospholipid-mediated signal transduction pathways resulting in cell proliferation. Demethoxyviridin (DMV), a structural analogue of wortmannin and recently reported as a potent inhibitor of phosphoinositide-3-kinase, inhibited bombesin plus insulin-stimulated increase in cell number in Swiss 3T3 cells, a model of cell proliferation. The drug produced cytostatic effects at concentrations below 1 mu M and cytotoxic effects at 10 mu M. In intact Swiss 3T3 cells DMV inhibited insulin-stimulated PI 3- and 4-kinases and bombesin-stimulated phospholipases C, D and A(2) in the nanomolar range. DMV also inhibited bombesin-stimulated tyrosine phosphorylation of a range of proteins at nM concentrations. This study shows that DMV inhibited multiple stimulated signalling pathways which lead to increased Swiss 3T3 cell proliferation. A stable analogue of DMV may have chemotherapeutic potential. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:29 / 38
页数:10
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