NFAT transcription factors: from cell cycle to tumor development

被引:70
作者
Viola, JPB [1 ]
Carvalho, LDS [1 ]
Fonseca, BPF [1 ]
Teixeira, LK [1 ]
机构
[1] Inst Nacl Canc, INCA, Div Biol Celular, BR-20231050 Rio De Janeiro, Brazil
关键词
NFAT; cell cycle; cancer; cell differentiation; gene expression;
D O I
10.1590/S0100-879X2005000300003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The nuclear factor of activated T cells (NFAT) family of transcription factors has been primarily identified in immune cells; however, these proteins have been recently found to be functionally active in several other non-immune cell types. NFAT proteins are activated upon different stimuli that lead to increased intracellular calcium levels. Regardless of their widely known cytokine gene expression properties, NFATs have been shown to regulate other genes related to cell cycle progression, cell differentiation and apoptosis, revealing a broader role for these proteins in normal cell physiology. Several reports have addressed the participation of NFATs in many aspects of malignant cell transformation and tumorigenic processes. In this review, we will discuss the involvement of the different NFAT family members in the regulation of cell cycling, differentiation and tumor formation, and also its implications on oncogenesis. Better understanding the mechanisms by which NFATs regulate cell cycle and tumor-related events should be relevant for the development of rational anti-cancer therapies.
引用
收藏
页码:335 / 344
页数:10
相关论文
共 60 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   CELL-CYCLE CONTROL BY CALCIUM AND CALMODULIN IN SACCHAROMYCES-CEREVISIAE [J].
ANRAKU, Y ;
OHYA, Y ;
IIDA, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1093 (2-3) :169-177
[3]   TH cell differentiation is accompanied by dynamic changes in histone acetylation of cytokine genes [J].
Avni, O ;
Lee, D ;
Macian, F ;
Szabo, SJ ;
Glimcher, LH ;
Rao, A .
NATURE IMMUNOLOGY, 2002, 3 (07) :643-651
[4]   Calcineurin regulation of the mammalian G0/G1 checkpoint element, cyclin dependent kinase 4 [J].
Baksh, S ;
DeCaprio, JA ;
Burakoff, SJ .
ONCOGENE, 2000, 19 (24) :2820-2827
[5]   NFATc2-mediated repression of cyclin-dependent kinase 4 expression [J].
Baksh, S ;
Widlund, HR ;
Frazer-Abel, AA ;
Du, JY ;
Fosmire, S ;
Fisher, DE ;
DeCaprio, JA ;
Modiano, JF ;
Burakoff, SJ .
MOLECULAR CELL, 2002, 10 (05) :1071-1081
[6]   Cell division is not a "clock" measuring acquisition of competence to produce IFN-γ or IL-4 [J].
Ben-Sasson, SZ ;
Gerstel, R ;
Hu-Li, J ;
Paul, WE .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :112-120
[7]   Helper T cell differentiation is controlled by the cell cycle [J].
Bird, JJ ;
Brown, DR ;
Mullen, AC ;
Moskowitz, NH ;
Mahowald, MA ;
Sider, JR ;
Gajewski, TF ;
Wang, CR ;
Reiner, SL .
IMMUNITY, 1998, 9 (02) :229-237
[8]   NFATC2 transcription factor regulates cell cycle progression during lymphocyte activation: evidence of its involvement in the control of cyclin gene expression [J].
Caetano, MS ;
Vieira-De-Abreu, A ;
Teixeira, LK ;
Werneck, MBF ;
Barcinski, MA ;
Viola, JPB .
FASEB JOURNAL, 2002, 16 (12) :1940-+
[9]   Autoregulation of NFATc1/A expression facilitates effector T cells to escape from rapid apoptosis [J].
Chuvpilo, S ;
Jankevics, E ;
Tyrsin, D ;
Akimzhanov, A ;
Moroz, D ;
Jha, MK ;
Luehrmann, JS ;
Santner-Nanan, B ;
Feoktistova, E ;
König, T ;
Avots, A ;
Schmitt, E ;
Berberich-Siebelt, F ;
Schimpl, A ;
Serfling, E .
IMMUNITY, 2002, 16 (06) :881-895
[10]   Induction of TH1 and TH2 CD4+ T cell responses: The alternative approaches [J].
Constant, SL ;
Bottomly, K .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :297-322