PHENYLACETATE SYNERGIZES WITH RETINOIC ACID IN INDUCING THE DIFFERENTIATION OF HUMAN NEUROBLASTOMA-CELLS

被引:44
作者
SIDELL, N
WADA, R
HAN, GY
CHANG, BS
SHACK, S
MOORE, T
SAMID, D
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,BRAIN RES INST,DEPT PATHOL & LAB MED NEUROPATHOL,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,SCH MED,JONSSON COMPREHENS CANC CTR,LOS ANGELES,CA 90024
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT PEDIAT,LOS ANGELES,CA 90024
[4] UNIV CALIF LOS ANGELES,SCH MED,GWYNNE HAZEN CHERRY MEM LABS,LOS ANGELES,CA 90024
[5] NCI,DIV CANC TREATMENT,CLIN PHARMACOL BRANCH,BETHESDA,MD 20892
关键词
D O I
10.1002/ijc.2910600414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phenylacetate, a natural metabolite of phenylalanine which was originally described as a plant growth hormone, has recently gained attention as a possible differentiation inducer for a variety of human tumor cell types. This interest prompted us to assess the ability of sodium phenylacetate (NaPA) to promote the differentiation of human neuroblastoma cells, both alone and in combination with retinoic acid (RA), a known inducer of neuroblastoma differentiation and maturation. Using the LA-N-5 cell line, we have determined that NaPA can stimulate the differentiation of neuroblastoma cells, as evidenced by dose-dependent inhibition of cell proliferation, neurite outgrowth, increased acetylcholinesterase activity and reduction of N-myc expression. Furthermore, NaPA and RA synergized in inducing differentiation, in that combination treatment resulted in cessation of cell growth along with morphologic and biochemical changes indicative of the loss of malignant properties. We have determined that NaPA can markedly enhance mRNA levels of the nuclear RA receptor-beta (RAR beta) in LA-N-5 cells prior to morphologic or other phenotypic changes induced by this compound. This effect appeared to be distinct from the ability of NaPA to alter tumor cell lipid metabolism via inhibition of protein isoprenylation. Thus among its varied effects on LA-N-5 cells, NaPA appears to interact with the RA pathway at the nuclear level by up-regulating RAR beta expression. (C) 1995 Wiley-Liss, Inc.
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页码:507 / 514
页数:8
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