C-terminal binding proteins: Emerging roles in cell survival and tumorigenesis

被引:51
作者
Bergman, L. M. [1 ]
Blaydes, J. P. [1 ]
机构
[1] Univ Southampton, Sch Med, Canc Sci Div, Southampton SO9 5NH, Hants, England
关键词
apoptosis; cancer; CtBP; Golgi; transcriptional repression;
D O I
10.1007/s10495-006-6651-4
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
Within a cell, the levels and activity of multiple pro- and anti-apoptotic molecules act in concert to regulate commitment to apoptosis. Whilst the balance between survival and death can be tipped by the effects of single molecules, cellular apoptosis control pathways very often incorporate key transcription factors that co-ordinately regulate the expression of multiple apoptosis control genes. C-terminal binding proteins (CtBPs), which were originally identified through their binding to the Adenovirus E1A oncoprotein, have been described as such transcriptional regulators of the apoptosis program. Specifically, CtBPs function as transcriptional co-repressors, and have been demonstrated to promote cell survival by suppressing the expression of several pro-apoptotic genes. In this review we summarize the evidence supporting a key role for CtBP proteins in cell survival. We also describe the known mechanisms of transcriptional control by CtBPs, and review the multiplicity of intracellular signaling and transcriptional control pathways with which they are known to be involved. Finally we consider these findings in the context of additional known roles of CtBP molecules, and the potential implications that this combined knowledge may have for our comprehension of diseases of cell survival, notably cancer.
引用
收藏
页码:879 / 888
页数:10
相关论文
共 117 条
[1]  
ALLISTON T, 2005, J BIOL CHEM
[2]   Nuclear speckle-associated protein Pnn/DRS binds to the transcriptional corepressor CtBP and relieves CtBP-mediated repression of the E-cadherin gene [J].
Alpatov, R ;
Munguba, GC ;
Caton, P ;
Joo, JH ;
Shi, Y ;
Shi, YJ ;
Hunt, ME ;
Sugrue, SP .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (23) :10223-10235
[3]   Nicotinamide adenine dinucleotide stimulates oligomerization, interaction with adenovirus E1A and an intrinsic dehydrogenase activity of CtBP [J].
Balasubramanian, P ;
Zhao, LJ ;
Chinnadurai, G .
FEBS LETTERS, 2003, 537 (1-3) :157-160
[4]   Functional inactivation of a transcriptional corepressor by a signaling kinase [J].
Barnes, CJ ;
Vadlamudi, RK ;
Mishra, SK ;
Jacobson, RH ;
Li, F ;
Kumar, R .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (08) :622-628
[5]   Correlation of Snail expression with histological grade and lymph node status in breast carcinomas [J].
Blanco, MJ ;
Moreno-Bueno, G ;
Sarrio, D ;
Locascio, A ;
Cano, A ;
Palacios, J ;
Nieto, MA .
ONCOGENE, 2002, 21 (20) :3241-3246
[6]  
BONAZZI M, 2005, NAT CELL BIOL
[7]   A REGION IN THE C-TERMINUS OF ADENOVIRUS-2/5 E1A PROTEIN IS REQUIRED FOR ASSOCIATION WITH A CELLULAR PHOSPHOPROTEIN AND IMPORTANT FOR THE NEGATIVE MODULATION OF T24-RAS MEDIATED TRANSFORMATION, TUMORIGENESIS AND METASTASIS [J].
BOYD, JM ;
SUBRAMANIAN, T ;
SCHAEPER, U ;
LAREGINA, M ;
BAYLEY, S ;
CHINNADURAI, G .
EMBO JOURNAL, 1993, 12 (02) :469-478
[8]  
Brannon M, 1999, DEVELOPMENT, V126, P3159
[9]   Mitotic Golgi partitioning is driven by the membrane-fissioning protein CtBP3/BARS [J].
Carcedo, CH ;
Bonazzi, M ;
Spanò, S ;
Turacchio, G ;
Colanzi, A ;
Luini, A ;
Corda, D .
SCIENCE, 2004, 305 (5680) :93-96
[10]   Multiple domains of the Receptor-Interacting Protein 140 contribute to transcription inhibition [J].
Castet, A ;
Boulahtouf, A ;
Versini, G ;
Bonnet, S ;
Augereau, P ;
Vignon, F ;
Khochbin, S ;
Jalaguier, S ;
Cavaillès, V .
NUCLEIC ACIDS RESEARCH, 2004, 32 (06) :1957-1966