Multiple faces of FoxM1 transcription factor Lessons from transgenic mouse models

被引:176
作者
Kalin, Tanya V. [1 ]
Ustiyan, Vladimir [1 ]
Kalinichenko, Vladimir V. [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Res Fdn, Perinatal Inst, Div Pulm Biol, Cincinnati, OH USA
[2] Cincinnati Childrens Hosp Res Fdn, Perinatal Inst, Div Dev Biol, Cincinnati, OH USA
关键词
winged helix DNA binding domain; forkhead transcription factor; FoxM1; embryonic development; cancer; cellular proliferation; cell cycle; transgenic mice; FORKHEAD BOX M1; DNA-BINDING-DOMAIN; BREAST-CANCER; S-PHASE; HEPATOCELLULAR CARCINOMAS; PULMONARY VASCULATURE; EMBRYONIC-DEVELOPMENT; CELL-PROLIFERATION; HEPATOCYTE ENTRY; TUMOR-SUPPRESSOR;
D O I
10.4161/cc.10.3.14709
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
FoxM1 transcription factor (previously called HFH-11B, Trident, FoxM1b, Win and MPP2) is expressed in actively dividing cells and critical for cell cycle progression. FoxM1 expression is induced in a variety of tissues during embryogenesis, and Foxm1(-/-) mice exhibit embryonic lethal phenotype due to multiple abnormalities in the liver, heart, lung and blood vessels. FoxM1 levels are dramatically decreased in adult tissues, but FoxM1 expression is re-activated during organ injury and numerous cancers. In this review, we discussed the role of FoxM1 in different cell lineages using recent data from transgenic mouse models with conditional "gain-of-function" and "loss-of-function" of FoxM1, as well as tissue samples from human patients. In addition, we provided experimental data showing additional sites of FoxM1 expression in the mouse embryo. Novel cell-autonomous roles of FoxM1 in embryonic development, organ injury and cancer formation in vivo were analyzed. Potential application of these findings for the diagnosis and treatment of human diseases were discussed.
引用
收藏
页码:396 / 405
页数:10
相关论文
共 77 条
[1]   Endothelial Cell-Specific Deletion of Transcription Factor FoxM1 Increases Urethane-Induced Lung Carcinogenesis [J].
Balli, David ;
Zhang, Yufang ;
Snyder, Jonathan ;
Kalinichenko, Vladimir V. ;
Kalin, Tanya V. .
CANCER RESEARCH, 2011, 71 (01) :40-50
[2]   Strong expression of FOXP1 identifies a distinct subset of diffuse large B-cell lymphoma (DLBCL) patients with poor outcome [J].
Barrans, SL ;
Fenton, JAL ;
Banham, A ;
Owen, RG ;
Jack, AS .
BLOOD, 2004, 104 (09) :2933-2935
[3]   Pro-proliferative FoxM1 is a target of p53-mediated repression [J].
Barsotti, A. M. ;
Prives, C. .
ONCOGENE, 2009, 28 (48) :4295-4305
[4]   Sequential dephosphorylation of p34(cdc2) on Thr-14 and Tyr-15 at the prophase/metaphase transition [J].
Borgne, A ;
Meijer, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) :27847-27854
[5]  
Brunetti-Pierri N., 2010, EUR J HUM GENET
[6]   Forkhead transcription factors: Key players in development and metabolism [J].
Carlsson, P ;
Mahlapuu, M .
DEVELOPMENTAL BIOLOGY, 2002, 250 (01) :1-23
[7]   CO-CRYSTAL STRUCTURE OF THE HNF-3/FORK HEAD DNA-RECOGNITION MOTIF RESEMBLES HISTONE-H5 [J].
CLARK, KL ;
HALAY, ED ;
LAI, ES ;
BURLEY, SK .
NATURE, 1993, 364 (6436) :412-420
[8]   IDENTIFICATION OF 9 TISSUE-SPECIFIC TRANSCRIPTION FACTORS OF THE HEPATOCYTE NUCLEAR FACTOR-III FORKHEAD DNA-BINDING-DOMAIN FAMILY [J].
CLEVIDENCE, DE ;
OVERDIER, DG ;
TAO, WF ;
QIAN, XB ;
PANI, L ;
LAI, EE ;
COSTA, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :3948-3952
[9]   New and unexpected: forkhead meets ARF [J].
Costa, RH ;
Kalinichenko, VV ;
Major, ML ;
Raychaudhuri, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2005, 15 (01) :42-48
[10]  
Costa RH, 2003, HEPATOLOGY, V38, p178A