Antitumor activity of sodium valproate in cultures of human neuroblastoma cells

被引:96
作者
Cinatl, J
Cinatl, J
Scholz, M
Driever, PH
Henrich, D
Kabickova, H
Vogel, JU
Doerr, HW
Kornhuber, B
机构
[1] UNIV FRANKFURT,ABT PADIATR HAMATOL & ONKOL,D-60590 FRANKFURT,GERMANY
[2] UNIV FRANKFURT,ZENTRUM HYG,ABT MED VIROL,ZENTRUM KINDERHEILKUNDE & JUGENDMED,D-60590 FRANKFURT,GERMANY
[3] UNIV FRANKFURT,ABT PADIATR NEUROL,D-60590 FRANKFURT,GERMANY
[4] UNIV FRANKFURT,GUSTAV EMBDEN ZENTRUM BIOL CHEM,D-60590 FRANKFURT,GERMANY
[5] KLINLAB STRESOVICE,PRAGUE 6,CZECH REPUBLIC
关键词
cell differentiation; lymphokine-activated neural cell adhesion molecule; neuroblastoma; sodium valproate;
D O I
10.1097/00001813-199609000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Valproic acid (VPA) is a simple branched-chain fatty acid that has anticonvulsant activity and is widely used in the treatment of epilepsy. VPA was found to effect growth and differentiation of human neuroblastoma (NB) cells in vitro at concentrations that have been achieved in humans with no significant adverse effects, Treatment of UKF-NB-2 and UKF-NB-3 NB cell lines with VPA at concentrations ranging from 0.5 to 2 mM resulted in neuronal morphological differentiation characterized by extension of cellular processes without significant effects on cell viability. Ultrastructural features of VPA-treated cells were consistent with the neuronal type of differentiation. VPA treatment of NB cells was associated with decreased expression of N-myc oncoprotein and increased expression of neural cell adhesion molecule in their membrane. Treatment of NB cells with 0.5 mM VPA increased their sensitivity to lymphokine-activated killer lysis. The results indicate that VPA, at non-toxic pharmacological concentrations, arrests the growth, induces differentiation and increases immunogenicity of NB cells through non-toxic mechanisms.
引用
收藏
页码:766 / 773
页数:8
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