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
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