Response to IL-6 of HPV-18 cervical carcinoma cell lines

被引:10
作者
Bauknecht, T
Randelzhofer, B
Schmitt, B
Ban, Z
Hernando, JJ
Bauknecht, T
机构
[1] Deutsch Krebsforschungszentrum, Forsch Schwerpunkt Angew Tumorvirol, D-69120 Heidelberg, Germany
[2] Univ Freiburg, Frauenklin, D-79106 Freiburg, Germany
关键词
D O I
10.1006/viro.1999.9722
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human papillomavirus type 18(HPV-18) upstream regulatory region (URR) controls cell type-specific expression of the viral oncoproteins E6 and E7. The HPV-18 URR is active in the cervical carcinoma cell line HeLa but inactive in the hepatoma cell line HepG2. C/EBP beta (NF-IL-6) was shown to participate as an important regulator in HPV transcription dependent on the cell type, The finding that C/EPB beta is critical for HPV-18 URR activity and that C/EPB beta is induced by IL-6 offers the opportunity of manipulating HPV activity by specific cytokine treatment In this report, we show that treatment with IL-6 results in activation of HPV-18 URR activity in HepG2 cells. In contrast, the HPV-18 URR is not inducible by IL-6 in three cervical carcinoma cell lines. In all three cell lines we found decreased expression of the IL-6 receptor compared to the IL-6-responsive HepG2 cells, whereas the level of expression of the signal transduction component gp130 is present in all cells. These results suggest that cervical carcinoma cells may circumvent the IL-6-induced cellular defense mechanism through downregulation of the IL-6-receptor, (C) 1999 Academic Press
引用
收藏
页码:344 / 354
页数:11
相关论文
共 68 条
[51]  
SEHGAL PB, 1990, P SOC EXP BIOL MED, V195, P183
[52]   ASSOCIATION AND ACTIVATION OF JAK-TYK KINASES BY CNTF-LIF-OSM-IL-6 BETA-RECEPTOR COMPONENTS [J].
STAHL, N ;
BOULTON, TG ;
FARRUGGELLA, T ;
IP, NY ;
DAVIS, S ;
WITTHUHN, BA ;
QUELLE, FW ;
SILVENNOINEN, O ;
BARBIERI, G ;
PELLEGRINI, S ;
IHLE, JN ;
YANCOPOULOS, GD .
SCIENCE, 1994, 263 (5143) :92-95
[53]   IN-VIVO CYTOKINE GENE-TRANSFER BY GENE GUN REDUCES TUMOR-GROWTH IN MICE [J].
SUN, WH ;
BURKHOLDER, JK ;
SUN, J ;
CULP, J ;
LU, XG ;
PUGH, TD ;
ERSHLER, WB ;
YANG, NS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2889-2893
[54]   CYTOKINE RECEPTORS AND SIGNAL TRANSDUCTION [J].
TAGA, T ;
KISHIMOTO, T .
FASEB JOURNAL, 1992, 6 (15) :3387-3396
[55]   Interleukin-6 (IL-6) production in carcinoma of the cervix [J].
Takano, H ;
Harigaya, K ;
Ishii, G ;
Sugaya, Y ;
Soeta, S ;
Nunoyama, T ;
Shirasawa, H ;
Shimizu, K ;
Tokita, H ;
Simizu, B ;
Mikata, A ;
Sekiya, S .
ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 1996, 258 (01) :25-33
[56]  
TAKIZAWA H, 1993, CANCER RES, V53, P4175
[57]  
TARTOUR E, 1994, CANCER RES, V54, P6243
[58]  
THIERRY F, 1987, CANCER CELL, V5, P23
[59]   INHIBITION OF TUMORIGENICITY OF CERVICAL-CANCER CELLS IN NUDE-MICE BY HPV E6-E7 ANTISENSE RNA [J].
VONKNEBEL, M ;
RITTMULLER, DC ;
HAUSEN, HZ ;
DURST, M .
INTERNATIONAL JOURNAL OF CANCER, 1992, 51 (05) :831-834
[60]   C/EBP beta is a negative regulator of human papillomavirus type 11 in keratinocytes [J].
Wang, H ;
Liu, K ;
Yuan, F ;
Berdichevsky, L ;
Taichman, LB ;
Auborn, K .
JOURNAL OF VIROLOGY, 1996, 70 (07) :4839-4844