Stat3 as an oncogene

被引:2628
作者
Bromberg, JF
Wrzeszczynska, MH
Devgan, G
Zhao, YX
Pestell, RG
Albanese, C
Darnell, JE
机构
[1] Rockefeller Univ, Mol Cell Biol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Mol Biophys, New York, NY 10021 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Albert Einstein Canc Ctr, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
关键词
D O I
10.1016/S0092-8674(00)81959-5
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
STATs are latent transcription factors that mediate cytokine- and growth factor-directed transcription. In many human cancers and transformed cell lines, Stat3 is persistently activated, and in cell culture, active Stat3 is either required for transformation, enhances transformation, or blocks apoptosis. We report that substitution of two cysteine residues within the C-terminal loop of the SH2 domain of Stat3 produces a molecule that dimerizes spontaneously, binds to DNA, and activates transcription. The Stat3-C molecule in immortalized fibroblasts causes cellular transformation scored by colony formation in soft agar and tumor formation in nude mice. Thus, the activated Stat3 molecule by itself can mediate cellular transformation and the experiments focus attention on the importance of constitutive Stat3 activation in human tumors.
引用
收藏
页码:295 / 303
页数:9
相关论文
共 49 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   POINT MUTATIONS WITHIN A DIMER INTERFACE HOMOLOGY DOMAIN OF C-MPL INDUCE CONSTITUTIVE RECEPTOR ACTIVITY AND TUMORIGENICITY [J].
ALEXANDER, WS ;
METCALF, D ;
DUNN, AR .
EMBO JOURNAL, 1995, 14 (22) :5569-5578
[3]  
Ausubel FM., 1994, Curr. Protoc. Mol. Biol
[4]   Molecular motions within the pore of voltage-dependent sodium channels [J].
Benitah, JP ;
Ranjan, R ;
Yamagishi, T ;
Janecki, M ;
Tomaselli, GF ;
Marban, E .
BIOPHYSICAL JOURNAL, 1997, 73 (02) :603-613
[5]  
Besser D, 1999, MOL CELL BIOL, V19, P1401
[6]   STAT3 ACTIVATION BY CYTOKINES UTILIZING GP130 AND RELATED TRANSDUCERS INVOLVES A SECONDARY MODIFICATION REQUIRING AN H7-SENSITIVE KINASE [J].
BOULTON, TG ;
ZHONG, Z ;
WEN, ZL ;
DARNELL, JE ;
STAHL, N ;
YANCOPOULOS, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) :6915-6919
[7]   Transcriptionally active Stat1 is required for the antiproliferative effects of both interferon alpha and interferon gamma [J].
Bromberg, JF ;
Horvath, CM ;
Wen, ZL ;
Schreiber, RD ;
Darnell, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7673-7678
[8]   Stat3 activation is required for cellular transformation by v-src [J].
Bromberg, JF ;
Horvath, CM ;
Besser, D ;
Lathem, WW ;
Darnell, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2553-2558
[9]   Constitutive activation of Stat3 signaling confers resistance to apoptosis in human U266 myeloma cells [J].
Catlett-Falcone, R ;
Landowski, TH ;
Oshiro, MM ;
Turkson, J ;
Levitzki, A ;
Savino, R ;
Ciliberto, G ;
Moscinski, L ;
Fernández-Luna, JL ;
Nuñez, G ;
Dalton, WS ;
Jove, R .
IMMUNITY, 1999, 10 (01) :105-115
[10]   Crystal structure of a tyrosine phosphorylated STAT-1 dimer bound to DNA [J].
Chen, XM ;
Vinkemeier, U ;
Zhao, YX ;
Jeruzalmi, D ;
Darnell, JE ;
Kuriyan, J .
CELL, 1998, 93 (05) :827-839