Opposing actions of STAT-1 and STAT-3

被引:134
作者
Stephanou, A [1 ]
Latchman, DS [1 ]
机构
[1] UCL, Inst Child Hlth, Med Mol Biol Unit, London WC1N 1EH, England
关键词
STAT-1; STAT-3; apoptosis; protein interaction; p53; DNA damage;
D O I
10.1080/08977190500178745
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The signal transducers and activators of transcription (STATs) are a family of transcription factors, which were originally identified on the basis of their ability to transduce a signal from a cellular receptor into the nucleus and modulate the transcription of specific genes. Interestingly, recent studies have demonstrated that STAT-1 plays a key role in promoting apoptosis in a variety of cell types, whereas STAT-3 has an anti-apoptotic effect. Moreover, whilst STAT-3 promotes cellular proliferation and is activated in a variety of tumour cells, STAT-1 appears to have an anti-proliferative effect. Although the initially characterised signal transduction events mediated by STAT-1 and STAT-3 involve the DNA binding and transcriptional activation domains of the factor, some of their other effects appear not to require DNA binding. Therefore, STAT-1 and STAT-3 can mediate the regulation of gene transcription both by direct DNA binding and via a co-activator mechanism and despite their very similar structures, have antagonistic effects on cellular proliferation and apoptosis.
引用
收藏
页码:177 / 182
页数:6
相关论文
共 46 条
  • [1] Cyclin D1 represses STAT3 activation through a Cdk4-independent mechanism
    Bienvenu, F
    Gascan, H
    Coqueret, O
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) : 16840 - 16847
  • [2] Stat3 as an oncogene
    Bromberg, JF
    Wrzeszczynska, MH
    Devgan, G
    Zhao, YX
    Pestell, RG
    Albanese, C
    Darnell, JE
    [J]. CELL, 1999, 98 (03) : 295 - 303
  • [3] Bromberg JF, 2001, BIOESSAYS, V23, P161, DOI 10.1002/1521-1878(200102)23:2<161::AID-BIES1023>3.0.CO
  • [4] 2-0
  • [5] Suppression of epithelial apoptosis and delayed mammary gland involution in mice with a conditional knockout of Stat3
    Chapman, RS
    Lourenco, PC
    Tonner, E
    Elint, DJ
    Selbert, S
    Takeda, K
    Akira, S
    Clarke, AR
    Watson, CJ
    [J]. GENES & DEVELOPMENT, 1999, 13 (19) : 2604 - 2616
  • [6] How Stat1 mediates constitutive gene expression: a complex of unphosphorylated Stat1 and IRF1 supports transcription of the LMP2 gene
    Chatterjee-Kishore, M
    Wright, KL
    Ting, JPY
    Stark, GR
    [J]. EMBO JOURNAL, 2000, 19 (15) : 4111 - 4122
  • [7] Cell growth arrest and induction of cyclin-dependent kinase inhibitor p21(WAF1/CIP1) mediated by STAT1
    Chin, YE
    Kitagawa, M
    Su, WCS
    You, ZH
    Iwamoto, Y
    Fu, XY
    [J]. SCIENCE, 1996, 272 (5262) : 719 - 722
  • [8] Specific inhibition of Stat3 signal transduction by PIAS3
    Chung, CD
    Liao, JY
    Liu, B
    Rao, XP
    Jay, P
    Berta, P
    Shuai, K
    [J]. SCIENCE, 1997, 278 (5344) : 1803 - 1805
  • [9] Mutational switch of an IL-6 response to an interferon-γ-like response
    Costa-Pereira, AP
    Tininini, S
    Strobl, B
    Alonzi, T
    Schlaak, JF
    Is'harc, H
    Gesualdo, I
    Newman, SJ
    Kerr, IM
    Poli, V
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) : 8043 - 8047
  • [10] SOCS3 negatively regulates IL-6 signaling in vivo
    Croker, BA
    Krebs, DL
    Zhang, JG
    Wormald, S
    Willson, TA
    Stanley, EG
    Robb, L
    Greenhalgh, CJ
    Förster, I
    Clausen, BE
    Nicola, NA
    Metcalf, D
    Hilton, DJ
    Roberts, AW
    Alexander, WS
    [J]. NATURE IMMUNOLOGY, 2003, 4 (06) : 540 - 545