The cell cycle and drug discovery: the promise and the hope

被引:34
作者
Brooks, G
La Thangue, NB
机构
[1] Profilix Ltd, Abingdon OX14 4RY, Oxon, England
[2] Univ Reading, Sch Anim & Microbial Sci, Reading RG6 6AJ, Berks, England
[3] Univ Glasgow, Div Biochem & Mol Biol, Glasgow G12 8QQ, Lanark, Scotland
关键词
D O I
10.1016/S1359-6446(99)01400-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, there have been major developments in the understanding of the cell cycle. It is now known that normal cellular proliferation is tightly regulated by the activation and deactivation of a series of proteins that constitute the cell cycle machinery. The expression and activity of components of the cell cycle can be altered during the development of a variety of diseases where aberrant proliferation contributes to the pathology of the illness. Apart from yielding a new source of untapped therapeutic targets, it is likely that manipulating the activity of such proteins in diseased states will provide an important route for treating proliferative disorders, and the opportunity to develop a novel class of future medicines.
引用
收藏
页码:455 / 464
页数:10
相关论文
共 96 条
[1]   Cell-cycle arrest and inhibition of Cdk4 activity by small peptides based on the carboxy-terminal domain of p21(WAF1) [J].
Ball, KL ;
Lain, S ;
Fahraeus, R ;
Smythe, C ;
Lane, DP .
CURRENT BIOLOGY, 1997, 7 (01) :71-80
[2]   Apoptosis induced in mammalian cells by small peptides that functionally antagonize the Rb-regulated E2F transcription factor [J].
Bandara, LR ;
Girling, R ;
LaThangue, NB .
NATURE BIOTECHNOLOGY, 1997, 15 (09) :896-901
[3]   Arresting developments in the cardiac myocyte cell cycle: Role of cyclin-dependent kinase inhibitors [J].
Brooks, G ;
Poolman, RA ;
Li, JM .
CARDIOVASCULAR RESEARCH, 1998, 39 (02) :301-311
[4]  
BROOKS G, 1998, BIOTCHNOLOGY HEALTHC, P131
[5]  
BUCKLEY MF, 1993, ONCOGENE, V8, P2127
[6]   ADENOVIRUS-MEDIATED OVER-EXPRESSION OF THE CYCLIN CYCLIN-DEPENDENT KINASE INHIBITOR, P21 INHIBITS VASCULAR SMOOTH-MUSCLE CELL-PROLIFERATION AND NEOINTIMA FORMATION IN THE RAT CAROTID-ARTERY MODEL OF BALLOON ANGIOPLASTY [J].
CHANG, MW ;
BARR, E ;
LU, MM ;
BARTON, K ;
LEIDEN, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2260-2268
[7]   CYTOSTATIC GENE-THERAPY FOR VASCULAR PROLIFERATIVE DISORDERS WITH A CONSTITUTIVELY ACTIVE FORM OF THE RETINOBLASTOMA GENE-PRODUCT [J].
CHANG, MW ;
BARR, E ;
SELTZER, J ;
JIANG, YQ ;
NABEL, GJ ;
NABEL, EG ;
PARMACEK, MS ;
LEIDEN, JM .
SCIENCE, 1995, 267 (5197) :518-522
[8]  
CHEN YM, 1991, ONCOGENE, V6, P1799
[9]   Selective killing of transformed cells by cyclin/cyclin-dependent kinase 2 antagonists [J].
Chen, YNP ;
Sharma, SK ;
Ramsey, TM ;
Jiang, L ;
Martin, MS ;
Baker, K ;
Adams, PD ;
Bair, KW ;
Kaelin, WG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4325-4329
[10]   Fungal infections [J].
Chimelli, L ;
MahlerAraujo, MB .
BRAIN PATHOLOGY, 1997, 7 (01) :613-627