Expression pattern of AP-2 transcription factors in cervical cancer cells and analysis of their influence on human papillomavirus oncogene transcription

被引:20
作者
Beger, M
Butz, K
Denk, C
Williams, T
Hurst, HC
Hoppe-Seyler, F
机构
[1] Deutsch Krebsforschungszentrum, Angew Tumorvirol, D-69120 Heidelberg, Germany
[2] Yale Univ, Sch Med, Dept Mol Cellular & Dev Biol, New Haven, CT 06510 USA
[3] Hammersmith Hosp, Imperial Canc Res Fund, Mol Oncol Unit, London W12 0NN, England
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2001年 / 79卷 / 5-6期
关键词
human papillomavirus; AP-2; cervical cancer; transcriptional regulation; c-erbB-2;
D O I
10.1007/s001090100211
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The AP-2 family of transcription factors consists of three known members, namely AP-2 alpha, AP-2 beta, and AP-2 gamma In experimental systems AP-2 factors, possess tumor suppressor-like activities, and alterations in the AP-2 expression pattern have been described for some tumor entities. In addition, AP-2 has been implicated in the transcriptional control of human papillomaviruses (HPVs). We investigated here the expression pattern of AP-2 alpha, AP-2 beta, and AP-2 gamma, as well as that of the cellular AP-2 target gene c-erbB-2, in a series of cervical cancer cell lines. In addition, we analyzed the influence of AP-2 factors on the activity of the HPV16 and HPV18 E6/E7 oncogene promoter. We found that, with the exception of HPV-negative C33A cells, all investigated cervical cancer cell lines expressed all three AP-2 family members, although at varying levels. No linear correlation between AP-2 and c-erbB-2 levels was observed. Although AP-2 alpha, AP-2 beta, and AP-2 gamma can activate the c-erbB-2 promoter in reporter gene assays, they do not stimulate the HPV 16 or HPV 18 E6/E7 promoter. These results indicate that, although a rare event, loss of AP-2 expression occurs in cervical cancer cells. Moreover, AP-2 alpha., AP-2 beta, and AP-2 gamma are neither sufficient nor required to activate the viral E6/E7 promoter.
引用
收藏
页码:314 / 320
页数:7
相关论文
共 31 条
[1]   RETINOIC ACID-MEDIATED REPRESSION OF HUMAN PAPILLOMAVIRUS-18 TRANSCRIPTION AND DIFFERENT LIGAND REGULATION OF THE RETINOIC ACID RECEPTOR BETA-GENE IN NONTUMORIGENIC AND TUMORIGENIC HELA HYBRID-CELLS [J].
BARTSCH, D ;
BOYE, B ;
BAUST, C ;
HAUSEN, HZ ;
SCHWARZ, E .
EMBO JOURNAL, 1992, 11 (06) :2283-2291
[2]   THE DEVELOPMENTALLY-REGULATED TRANSCRIPTION FACTOR AP-2 IS INVOLVED IN C-ERBB-2 OVEREXPRESSION IN HUMAN MAMMARY-CARCINOMA [J].
BOSHER, JM ;
WILLIAMS, T ;
HURST, HC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :744-747
[3]  
Bosher JM, 1996, ONCOGENE, V13, P1701
[4]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[5]   TRANSCRIPTIONAL CONTROL OF HUMAN PAPILLOMAVIRUS (HPV) ONCOGENE EXPRESSION - COMPOSITION OF THE HPV TYPE-18 UPSTREAM REGULATORY REGION [J].
BUTZ, K ;
HOPPESEYLER, F .
JOURNAL OF VIROLOGY, 1993, 67 (11) :6476-6486
[6]   Uncoupling of p21WAF1/CIP1/SDI1 mRNA and protein expression upon genotoxic stress [J].
Butz, K ;
Geisen, C ;
Ullmann, A ;
Zentgraf, H ;
Hoppe-Seyler, F .
ONCOGENE, 1998, 17 (06) :781-787
[7]  
BUTZ K, 1995, ONCOGENE, V10, P927
[8]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[9]   Control of HPV 18 DNA replication by cellular and viral transcription factors [J].
Demeret, C ;
LeMoal, M ;
Yaniv, M ;
Thierry, F .
NUCLEIC ACIDS RESEARCH, 1995, 23 (23) :4777-4784
[10]   THE EPIDERMIS - RISING TO THE SURFACE [J].
FUCHS, E ;
BYRNE, C .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (05) :725-736