MODULATION OF POMC EXPRESSION IN HUMAN NEUROECTODERMAL CELLS

被引:9
作者
DELAURENZI, V
MELINO, G
KNIGHT, RA
PIEROTTI, AR
COHEN, P
机构
[1] NATL HEART & LUNG INST,DEPT CYST FIBROSIS,LONDON SW3 6LY,ENGLAND
[2] UNIV PARIS 06,BIOCHIM SIGNAUX REGULATEURS CELLULAIRES & MOLEC LAB,CNRS,URA 1682,F-75006 PARIS,FRANCE
关键词
D O I
10.1006/bbrc.1993.2633
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
Neuroblastoma cell lines have been reported to contain two proopiomelanocortin (POMC) mRNA transcripts. We have now shown by immunocytochemistry and radioimmunoassay (RIA) that a number of neuroectodermally derived cell lines contain immunoreactive β-endorphin although cell concentrations were not characteristic of any tumour type. To explore further the functional significance of β-endorphin expression, we analysed neuroblastoma cell lines having intermediate (I), substrate adherent (S) and neuronal (N) phenotypes. No differences in cell β-endorphin content were detected. However, the expression of POMC mRNA and of immunoreactive β- endorphin was reduced within a few hours of treatment of these cell lines with retinoic acid. Culture of the cell lines in the presence of β-endorphin resulted in small but significant increases in growth. Although the POMC gene is in the same chromosomal segment as N-myc, which is normally amplified in neuroblastoma, no corresponding amplification of POMC could be demonstrated. The data suggest that POMC gene products may contribute to the autocrine/paracrine growth of neuroectodermal tumours. © 1993 Academic Press, Inc.
引用
收藏
页码:1402 / 1409
页数:8
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