Forkhead box proteins: tuning forks for transcriptional harmony

被引:559
作者
Lam, Eric W. -F. [1 ]
Brosens, Jan J. [2 ]
Gomes, Ana R. [1 ]
Koo, Chuay-Yeng [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Surg & Canc, Imperial Ctr Translat & Expt Med ICTEM, London W12 0NN, England
[2] Univ Hosp, Div Reprod Hlth, Warwick Med Sch, Clin Sci Res Labs, Coventry CV2 2DX, W Midlands, England
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; ESTROGEN-RECEPTOR-ALPHA; BREAST-CANCER CELLS; ANDROGEN RECEPTOR; HISTONE DEACETYLASES; FOXM1; EXPRESSION; PROSTATE-CANCER; SUPPRESSOR GENE; FACTOR FOXO3A; ER-ALPHA;
D O I
10.1038/nrc3539
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Forkhead box (FOX) proteins are multifaceted transcription factors that are responsible for fine-tuning the spatial and temporal expression of a broad range of genes both during development and in adult tissues. This function is engrained in their ability to integrate a multitude of cellular and environmental signals and to act with remarkable fidelity. Several key members of the FOXA, FOXC, FOXM, FOXO and FOXP subfamilies are strongly implicated in cancer, driving initiation, maintenance, progression and drug resistance. The functional complexities of FOX proteins are coming to light and have established these transcription factors as possible therapeutic targets and putative biomarkers for specific cancers.
引用
收藏
页码:482 / 495
页数:14
相关论文
共 196 条
[61]   Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes [J].
Howarth, K. D. ;
Blood, K. A. ;
Ng, B. L. ;
Beavis, J. C. ;
Chua, Y. ;
Cooke, S. L. ;
Raby, S. ;
Ichimura, K. ;
Collins, V. P. ;
Carter, N. P. ;
Edwards, P. A. W. .
ONCOGENE, 2008, 27 (23) :3345-3359
[62]   Foxp1 is an essential transcriptional regulator of B cell development [J].
Hu, Hui ;
Wang, Bin ;
Borde, Madhuri ;
Nardone, Julie ;
Maika, Shan ;
Allred, Laura ;
Tucker, Philip W. ;
Rao, Anjana .
NATURE IMMUNOLOGY, 2006, 7 (08) :819-826
[63]   IκB kinase promotes tumorigenesis through inhibition of forkhead FOXO3a [J].
Hu, MCT ;
Lee, DF ;
Xia, WY ;
Golfman, LS ;
Fu, OY ;
Yang, JY ;
Zou, YY ;
Bao, SL ;
Hanada, N ;
Saso, H ;
Kobayashi, R ;
Hung, MC .
CELL, 2004, 117 (02) :225-237
[64]   A Novel FoxM1-Caveolin Signaling Pathway Promotes Pancreatic Cancer Invasion and Metastasis [J].
Huang, Chen ;
Qiu, Zhengjun ;
Wang, Liwei ;
Peng, Zhihai ;
Jia, Zhiliang ;
Logsdon, Craig D. ;
Le, Xiangdong ;
Wei, Daoyan ;
Huang, Suyun ;
Xie, Keping .
CANCER RESEARCH, 2012, 72 (03) :655-665
[65]   Skp2 inhibits FOX01 in tumor suppression through ubiquitin-mediated degradation [J].
Huang, H ;
Regan, KM ;
Wang, F ;
Wang, DP ;
Smith, DI ;
van Deursen, JMA ;
Tindall, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (05) :1649-1654
[66]   CDK2-dependent phosphorylation of FOXO1 as an apoptotic response to DNA damage [J].
Huang, Haojie ;
Regan, Kevin M. ;
Lou, Zhenkun ;
Chen, Junjie ;
Tindall, Donald J. .
SCIENCE, 2006, 314 (5797) :294-297
[67]   The forkhead transcription factor FOXO3a increases phosphoinositide-3 kinase/Akt activity in drug-resistant leukemic cells through induction of PIK3CA expression [J].
Hui, Rosaline C. -Y. ;
Gomes, Ana R. ;
Constantinidou, Demetra ;
Costa, Joana R. ;
Karadedou, Christina T. ;
de Mattos, Silvia Fernandez ;
Wymann, Matthias P. ;
Brosens, Jan J. ;
Schulze, Almut ;
Lam, Eric W. -F. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (19) :5886-5898
[68]   Doxorubicin activates FOXO3a to induce the expression of multidrug resistance gene ABCB1 (MDR1) in K562 leukemic cells [J].
Hui, Rosaline C-Y. ;
Francis, Richard E. ;
Guest, Stephanie K. ;
Costa, Joana R. ;
Gomes, Ana R. ;
Myatt, Stephen S. ;
Brosens, Jan J. ;
Lam, Eric W-F. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (03) :670-678
[69]  
Jackson Brian C., 2010, Human Genomics, V4, P345
[70]   FoxO6, a novel member of the FoxO class of transcription factors with distinct shuttling dynamics [J].
Jacobs, FMJ ;
van der Heide, LP ;
Wijchers, PJEC ;
Burbach, JPH ;
Hoekman, MFM ;
Smidt, MP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :35959-35967