Cooperative activity between HER oncogenes and the tumor suppressor IRF-1 results in apoptosis

被引:41
作者
Kirchhoff, S [1 ]
Hauser, H [1 ]
机构
[1] GBF, Natl Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany
关键词
interferon regulatory factor-1; HER; apoptosis; cell growth; STAT5; transcriptional activity;
D O I
10.1038/sj.onc.1202704
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 tumor suppressor transcription factor IRE-I inhibits cell growth. In this report we show that IRF-1 also induces apoptosis of highly transformed and tumorigenic cell lines. This activity of IRF-1 is demonstrated with cell lines expressing HER oncogenes and an activatable IRE-I fusion protein. Growth of cell lines expressing inactive HER1 is inhibited on IRE-I activation. In contrast, the same cells are killed by apoptosis when HER1 and IRE-I are activated simultaneously. We identified promoters stimulated synergistically by IRF-1 and by activated HER1. To determine the signals causing transcriptional synergism and/or apoptosis we tried to modulate these effects by various dominant negative acting proteins. Dominant negative STAT5 alpha: abolished both induction of apoptosis and transcriptional synergy of IRF-1 and HER. Thus, these results provide new insights into the mechanism of oncogene-dependent apoptosis induced by the activation of a tumor suppressor.
引用
收藏
页码:3725 / 3736
页数:12
相关论文
共 82 条
[1]   12-O-TETRADECANOYL-PHORBOL-13-ACETATE INDUCTION OF THE HUMAN COLLAGENASE GENE IS MEDIATED BY AN INDUCIBLE ENHANCER ELEMENT LOCATED IN THE 5'-FLANKING REGION [J].
ANGEL, P ;
BAUMANN, I ;
STEIN, B ;
DELIUS, H ;
RAHMSDORF, HJ ;
HERRLICH, P .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (06) :2256-2266
[2]   VECTORS FOR EFFICIENT EXPRESSION IN MAMMALIAN FIBROBLASTOID, MYELOID AND LYMPHOID-CELLS VIA TRANSFECTION OR INFECTION [J].
ARTELT, P ;
MORELLE, C ;
AUSMEIER, M ;
FITZEK, M ;
HAUSER, H .
GENE, 1988, 68 (02) :213-219
[3]   Transcriptional activation by p53, but not induction of the p21 gene, is essential for oncogene-mediated apoptosis [J].
Attardi, LD ;
Lowe, SW ;
Brugarolas, J ;
Jacks, T .
EMBO JOURNAL, 1996, 15 (14) :3693-3701
[4]  
Baasner S, 1996, ONCOGENE, V13, P901
[5]  
BACUS SS, 1994, AM J CLIN PATHOL, V102, pS13
[6]   INTERFERON-RESPONSIVE REGULATORY ELEMENTS IN THE PROMOTER OF THE HUMAN 2',5'-OLIGO(A) SYNTHETASE GENE [J].
BENECH, P ;
VIGNERON, M ;
PERETZ, D ;
REVEL, M ;
CHEBATH, J .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (12) :4498-4504
[7]  
Biscardi JS, 1998, MOL CARCINOGEN, V21, P261, DOI 10.1002/(SICI)1098-2744(199804)21:4<261::AID-MC5>3.0.CO
[8]  
2-N
[9]   HYGROMYCIN-B PHOSPHOTRANSFERASE AS A SELECTABLE MARKER FOR DNA TRANSFER EXPERIMENTS WITH HIGHER EUKARYOTIC CELLS [J].
BLOCHLINGER, K ;
DIGGELMANN, H .
MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (12) :2929-2931
[10]   Positive selection of apoptosis-resistant cells correlates with activation of dominant-negative STAT5 [J].
Bovolenta, C ;
Testolin, L ;
Benussi, L ;
Lievens, PMJ ;
Liboi, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (33) :20779-20784