ATF2 on the double - activating transcription factor and DNA damage response protein

被引:80
作者
Bhoumik, Anindita [1 ]
Lopez-Bergami, Pablo [1 ]
Ronai, Ze'ev [1 ]
机构
[1] Burke Med Res Inst, Signal Transduc Program, La Jolla, CA USA
来源
PIGMENT CELL RESEARCH | 2007年 / 20卷 / 06期
关键词
ATF2; transcription; DNA damage; stress response; hypoxia; skin cancer; melanoma;
D O I
10.1111/j.1600-0749.2007.00414.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Signal transduction pathways play a key role in the regulation of key cellular processes, including survival and death. Growing evidence points to changes in signaling pathway that occur during skin tumor development and progression. Such changes impact the activity of downstream substrates, including transcription factors. The activating transcription factor 2 (ATF2) has been implicated in malignant and non-malignant skin tumor developments. ATF2 mediates both transcription and DNA damage control, through its phosphorylation by JNK/p38 or ATM/ATR respectively. Here, we summarize our present understanding of ATF2 regulation, function and contribution to malignant and non-malignant skin tumor development.
引用
收藏
页码:498 / 506
页数:9
相关论文
共 90 条
[1]  
ABBAS S, IN PRESS CLIN CANC R
[2]   Epstein-Barr virus immediate-early proteins BZLF1 and BRLF1 activate the ATF2 transcription factor by increasing the levels of phosphorylated p38 and c-Jun N-terminal kinases [J].
Adamson, AL ;
Darr, D ;
Holley-Guthrie, E ;
Johnson, RA ;
Mauser, A ;
Swenson, J ;
Kenney, S .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1224-1233
[3]   Identification of human myometrial target genes of the c-Jun NH2-terminal kinase (JNK) pathway:: the role of activating transcription factor 2 (ATF2) and a novel spliced isoform ATF2-small [J].
Bailey, J ;
Europe-Finner, GN .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2005, 34 (01) :19-35
[4]  
Bailey J, 2002, J CLIN ENDOCR METAB, V87, P1717, DOI 10.1210/jc.87.4.1717
[5]  
Berger AJ, 2003, CANCER RES, V63, P8103
[6]   p38 MAPK-mediated transcriptional activation of inducible nitric-oxide synthase in glial cells -: Roles of nuclear factors, nuclear factor κB, cAMP response element-binding protein, ccaat/enhancer-binding protein-β, and activating transcription factor-2 [J].
Bhat, NR ;
Feinstein, DL ;
Shen, Q ;
Bhat, AN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (33) :29584-29592
[7]   ATM-dependent phosphorylation of ATF2 is required for the DNA damage response [J].
Bhoumik, A ;
Takahashi, S ;
Breitweiser, W ;
Shiloh, Y ;
Jones, N ;
Ronai, Z .
MOLECULAR CELL, 2005, 18 (05) :577-587
[8]   An ATF2-derived peptide sensitizes melanomas to apoptosis and inhibits their growth and metastasis [J].
Bhoumik, A ;
Huang, TG ;
Ivanov, V ;
Gangi, L ;
Qiao, RF ;
Woo, SLC ;
Chen, SH ;
Ronai, Z .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 110 (05) :643-650
[9]   Inhibition of melanoma growth and metastasis by ATF2-derived peptides [J].
Bhoumik, A ;
Gangi, L ;
Ronai, Z .
CANCER RESEARCH, 2004, 64 (22) :8222-8230
[10]   Transcriptional switch by activating transcription factor 2-derived peptide sensitizes melanoma cells to apoptosis and inhibits their tumorigenicity [J].
Bhoumik, A ;
Jones, N ;
Ronai, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (12) :4222-4227