The effect of cellular retinoic acid binding protein-I expression on the CYP26-mediated catabolism of all-trans retinoic acid and cell proliferation in head and neck suuamous cell carcinoma

被引:31
|
作者
Won, JY
Nam, EC
Yoo, SJ
Kwon, HJ
Um, SJ
Han, HS
Kim, SH
Byun, Y
Kim, SY
机构
[1] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Otolaryngol, Seoul 138736, South Korea
[2] Univ Kangwon, Coll Med, Dept Otolaryngol, Chunchon, South Korea
[3] Sejong Univ, Dept Biosci & Biotechnol, Inst Biosci, Seoul, South Korea
[4] Sungkyunkwan Univ, Coll Med, Samsung Med Ctr, Dept Clin Pathol, Seoul, South Korea
[5] Kwangju Inst Sci & Technol, Dept Mat Sci & Engn, Kwangju, South Korea
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2004年 / 53卷 / 08期
关键词
D O I
10.1016/j.metabol.2003.12.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to confirm if catabolism of all-trans retinoic acid (RA) is enhanced by type 1 cellular retinoic acid binding protein (CRABP-1) expression and to investigate the effect of this enhanced catabolism on cell proliferation of the head and neck squamous cell carcinoma (HNSCC) cell line, AMC-HN-7. We also analyzed the effects of CRABP-1 on RA-induced retinoic acid receptor (RAR) activity. The expression of the CRABP-1 in stably transfected AMC-HN-7 cell lines (HN7-BPIa and HN7-BP1b) resulted in a lower sensitivity to administered RA compared with that of controls in a clonogenic assay. HN7-BPIs cells showed an increased amount of polar metabolites of RA in thin-layer chromatography. The transcriptional activity of the reporter plasmid RARE(DR5)-tk-CAT after the treatment of RA was lesser in HN7-BPIs than in controls. These results suggest that the increased CYP26-mediated catabolism of RA by CRABP-1 transfection might decrease the amount of RA that is accessible to the nuclear receptors and make HNSCC cells resistant to RA. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1007 / 1012
页数:6
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