E2F transcription factors and cancerFactores de transcripción E2F y cáncer

被引:0
作者
Jaume Piulats
Gema Tarrasón
机构
[1] Merck Farma y Química,Laboratorio de Bioinvestigación
来源
Revista de Oncología | 2001年 / 3卷 / 5期
关键词
E2F; cancer; apoptosis; E2F; cáncer; apoptosis;
D O I
10.1007/BF02719883
中图分类号
学科分类号
摘要
Tumor cells have developed successful mechanisms to escape the normal controls that regulate cell proliferation and apoptosis. Basic research can help in the processes of target discovery for designing new therapeutic interventions in oncology based on the control of the cell cycle. As alterations in gene expression have become a better understood component of normal development and disease progression, transcription factors have become an increasingly attractive target for therapy. The aim of this article is to review the role of the E2F family of transcription factors in the control of the cell cycle of normal and cancerous cells, as well as to give an outline of their potential as targets for therapy.
引用
收藏
页码:241 / 249
页数:8
相关论文
共 327 条
[1]  
Avantaggiati ML(2000)Molecular horizons of cancer therapeutics 11th Pezcoller Symposium Biochim Biophys Acta 1.470 R49-R59
[2]  
Stiewe T(2000)Role of the p53-homologue p73 in E2F-1—induced apoptosis Nature Genetics 26 464-469
[3]  
Pützer B(1999)The cell cycle and drug discovery: the promise and the hope Drug Discovery Today 4 455-464
[4]  
Brooks G(1994)Cell cycle checkpoints Curr Opin Cell Biol 6 872-876
[5]  
La Thange NB(1999)Cell proliferation and apoptosis Curr Opin Cell Biol 11 745-752
[6]  
Mirray A(1994)Cell cycle control and cancer Science 266 1.821-1.828
[7]  
Guo M(1988)Purification of maturation-promoting factor, an intracellular regulator of early mitotic events Proc Natl Acad Sci USA 85 3.009-3.013
[8]  
Hay B(1988)The xenopus cdc 2 protein is a component of MPF, a cytoplasmic regulator of mitosis Cell 54 423-431
[9]  
Hartwell L(1991)odc 25 is a specific tyrosine phosphatase that directly activates p34 Cell 67 197-211
[10]  
Kastan M(1994)The decision to enter mitosis Trends Cell Biol 4 202-207