Expression and retinoid modulation of N-arginine dibasic convertase and an aminopeptidase-B in human neuroblastoma cell lines

被引:13
作者
Draoui, M
Bellincampi, L
Hospital, V
Cadel, S
Foulon, T
Prat, A
Barre, N
Reichert, U
Melino, G
Cohen, P
机构
[1] UNIV PARIS 06,URA CNRS 1682,LAB BIOCHIM SIGNAUX REGULATEURS CELLULAIRES & MOL,F-75006 PARIS,FRANCE
[2] UNIV ROMA TOR VERGATA,DEPT EXPT MED,BIOCHEM LAB,IRCCS,IDI,ROME,ITALY
[3] UNIV AQUILA,DEPT BIOL,I-67100 LAQUILA,ITALY
[4] CIRD GALDERMA,SOPHIA ANTIPOLIS,FRANCE
关键词
neuroblastoma; retinoic acid; NRII convertase; aminopeptidase-beta; apoptosis;
D O I
10.1023/A:1005745717231
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Under retinoic acid exposure, the three SK-N-BE(2)-derived human neuroblastoma cell lines, BE(2)-NA, BE(2)-SA and BE(2)-M17 undergo mainly differentiation, apoptosis or continue to proliferate, respectively. We have used this model system to study the modulation of the transcriptional expression of putative processing enzymes, two novel metallopeptidases; i.e. N-arginine dibasic convertase (NRD convertase; EC 3.4.24.61) and an aminopeptidase-B after exposure of the cells either to retinoic acid or to synthetic retinoid analogs. The data indicate that the two respective enzymes are differently modulated in the various cell lines. Whereas aminopeptidase-B expression is enhanced in most cases, NRD convertase appears to undergo opposite regulation in proliferating versus differentiating neuroblastoma cells. It is concluded that both genes might contain retinoic acid regulatory elements (RARE) in their promoters.
引用
收藏
页码:99 / 106
页数:8
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