Inducible phosphorylation or dephosphorylation of transcription factors is an important mechanism of signal-dependent gene regulation in eukaryotic cells. This paper describes a combination of techniques that can be used to study the effect of this covalent protein modification on the DNA-binding ac
The effect of schedule, protein binding and growth factors on the activity of suramin
โ Scribed by Rafael Lopez Lopez; Godefridus J. Peters; Arie C. van Loenen; Paulo E. Pizao; Ruud E. N. van Rijswijk; John Wagstaff; Herbert M. Pinedo
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- French
- Weight
- 667 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Suramin has been shown to have antiproliferative activity, either by blocking the binding of growth factors to their receptors or by inhibiting critical cellular enzymes. In 6 different cell lines from 5 tumour types (MCFโ7, MCFโ7/ADR^R^, PC3, HTโ29, UMโSCCโIIB and SWโ1573/1R500), we studied the effect of scheduling of suramin, of FCS and of human serum albumin (HSA), of epidermal growth factor (EGF) and of the addition of growth factors in serumโfree medium on the activity of suramin. The concentration of suramin which gave 50% growth inhibition (IC~50~) varied from 45 ฮผM in SWโI573/IR500 to 153 ฮผM in PC3 cells grown in medium supplemented with 5% FCS, after 6 days of continuous exposure. Exposure for more than 4 days did not enhance the sensitivity to suramin, except in PC3. At exposure to suramin for 1 day followed by 5 days recovery, high IC~50~ values (>0.5 mM) were observed in MCFโ7 cells. In medium with 1% and 0.5% FCS these values were 3 to 8 and 14 to 26 times lower respectively. Addition of HSA increased the IC~50~ in PC3 and MCFโ7 cells. Suramin binding to protein was dependent on the concentration of protein and of suramin. Excess of EGF in medium with different FCS concentrations did not change the IC~50~ values of suramin in PC3 and MCFโ7 cells. Addition of EGF, fibroblast growth factor or plateletโderived growth factor in PC3 cells cultured in serumโfree medium did not increase the IC~50~ values. Suramin was active against these 6 cell lines at clinically achievable concentrations. This activity varied depending on the cell line, exposure time and suramin concentration. The most significant factor interfering with sensitivity to suramin was the amount of protein present in the culture medium.
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