Molecular cloning of human squamous cell carcinoma antigen 1 gene and characterization of its promoter

被引:14
作者
Hamada, K [1 ]
Shinomiya, H
Asano, Y
Kihana, T
Iwamoto, M
Hanakawa, Y
Hashimoto, K
Hirose, S
Kyo, S
Ito, M
机构
[1] Ehime Univ, Sch Med, Dept Obstet & Gynecol, Shigenobu, Ehime 7910295, Japan
[2] Ehime Univ, Sch Med, Dept Bacteriol, Shigenobu, Ehime 7910295, Japan
[3] Ehime Univ, Sch Med, Dept Dermatol, Shigenobu, Ehime 7910295, Japan
[4] Natl Inst Genet, Dept Dev Genet, Shizuoka 4118540, Japan
[5] Kanazawa Univ, Sch Med, Dept Obstet & Gynecol, Kanazawa, Ishikawa 9200934, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2001年 / 1518卷 / 1-2期
关键词
squamous cell carcinoma antigen 1; squamous cell carcinoma antigen 2; luciferase assay; squamous cell carcinoma; promoter; nucleotide sequence;
D O I
10.1016/S0167-4781(01)00174-9
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
The squamous cell carcinoma antigen (SCCA) serves as a serological marker for squamous cell carcinomas. Molecular cloning of the SCCA genomic region has revealed the presence of two tandemly arrayed genes, SCCA1 and SCCA2, which are 95% identical in nucleotide sequence. SCCA1 is a papain-like cysteine proteinase inhibitor, while SCCA2 is a chymotrypsin-like serine proteinase inhibitor. We analyzed here the sequence and the promoter activity of the 5'-flanking region of the SCCA1 gene. Deletion analysis of SCCA1 and SCCA2 promoter identified a 471-bp core promoter region upstream of the transcription start site. The transcriptional activity of SCCA1 promoter was up-regulated in squamous cell carcinoma cells, compared with keratinocyte and adenocarcinoma cells. The ratios of SCCA1 to SCCA2 promoter activity in squamous cell carcinoma, keratinocyte and adenocarcinoma cells were respectively 1.6. 5.3 and 2.8. Position -50 of SCCA1 and SCCA2 promoters played an important role in determining the promoter activities of SCCA1 and SCCA2. These findings suggest that the transcriptional regulation of SCCA1 and SCCA2 might differ among squamous cell carcinoma, keratinocyte and adenocarcinoma cells, and that SCCA1 promoter might be a potential target of gene therapy for squamous cell carcinoma. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:124 / 131
页数:8
相关论文
共 16 条
[1]   SQUAMOUS-CELL CARCINOMA ANTIGEN - CLINICAL UTILITY IN SQUAMOUS-CELL CARCINOMA OF THE UTERINE CERVIX [J].
BOLLI, JAN ;
DOERING, DL ;
BOSSCHER, JR ;
DAY, TG ;
RAO, CV ;
OWENS, K ;
KELLY, B ;
GOLDSMITH, J .
GYNECOLOGIC ONCOLOGY, 1994, 55 (02) :169-173
[2]   Association of transcriptionally silent genes with Ikaros complexes at centromeric heterochromatin [J].
Brown, KE ;
Guest, SS ;
Smale, ST ;
Hahm, K ;
Merkenschlager, M ;
Fisher, AG .
CELL, 1997, 91 (06) :845-854
[3]   CANCER OF THE UTERINE CERVIX - SENSITIVITY AND SPECIFICITY OF SERUM SQUAMOUS-CELL CARCINOMA ANTIGEN DETERMINATIONS [J].
DUK, JM ;
DEBRUIJN, HWA ;
GROENIER, KH ;
HOLLEMA, H ;
TENHOOR, KA ;
KRANS, M ;
AALDERS, JG .
GYNECOLOGIC ONCOLOGY, 1990, 39 (02) :186-194
[4]  
KATO H, 1977, CANCER, V40, P1621, DOI 10.1002/1097-0142(197710)40:4<1621::AID-CNCR2820400435>3.0.CO
[5]  
2-I
[6]   LYF-1, A TRANSCRIPTIONAL REGULATOR THAT INTERACTS WITH A NOVEL CLASS OF PROMOTERS FOR LYMPHOCYTE-SPECIFIC GENES [J].
LO, K ;
LANDAU, NR ;
SMALE, ST .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (10) :5229-5243
[7]   THE IKAROS GENE ENCODES A FAMILY OF FUNCTIONALLY DIVERSE ZINC-FINGER DNA-BINDING PROTEINS [J].
MOLNAR, A ;
GEORGOPOULOS, K .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8292-8303
[8]  
Rodriguez R, 1997, CANCER RES, V57, P2559
[9]   Structural analysis of human SCC antigen 2 promoter [J].
Sakaguchi, Y ;
Kishi, F ;
Murakami, A ;
Suminami, Y ;
Kato, H .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1444 (01) :111-116
[10]   A SERINE PROTEINASE-INHIBITOR LOCUS AT 18Q21.3 CONTAINS A TANDEM DUPLICATION OF THE HUMAN SQUAMOUS-CELL CARCINOMA ANTIGEN GENE [J].
SCHNEIDER, SS ;
SCHICK, C ;
FISH, KE ;
MILLER, E ;
PENA, JC ;
TRETER, SD ;
HUI, SM ;
SILVERMAN, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3147-3151