Systems biology and the molecular circuits of cancer

被引:31
作者
Alberghina, L [1 ]
Chiaradonna, F [1 ]
Vanoni, M [1 ]
机构
[1] Univ Milano Bicocca, Dept Biosci & Biotechnol, I-20126 Milan, Italy
关键词
antitumor agents; cell cycles; metabolism; modeling; signal transduction; systems biology;
D O I
10.1002/cbic.200400170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proliferative disorders are a major challenge for human health. The understanding of the organization of cell-cycle events is of the utmost importance to devise effective therapeutic strategies for cancer. The awareness that cells and organisms are complex, modular, hierarchical systems and the availability of genome-wide gene expression and protein analyses, should make it feasible to elucidate human diseases in terms of dysfunctions of molecular systems. Here we review evidence in support of a systems model of the cell cycle, in which two sequential growth-sensitive thresholds control entry into S-phase. The putative molecular determinants that set the threshold for entry into S-phase are consistently altered in cancer cells. Such a framework could be useful in guiding both experimental investigation and data analysis by allowing wiring to other relevant cell modules thereby highlighting the differential responses, or lack of response of cancer cells to intra- and extracellular factors. Pharmacological approaches that take advantage of transformation-induced fragility to glucose shortage are discussed. Extension of this hierarchical, modular approach to tumors as a whole holds promise for the development of effective drug discovery approaches and more efficient therapeutic protocols.
引用
收藏
页码:1322 / 1333
页数:12
相关论文
共 109 条
[1]   A BIMOLECULAR MECHANISM FOR THE CELL-SIZE CONTROL OF THE CELL-CYCLE [J].
ALBERGHINA, L ;
MARTEGANI, E ;
MARIANI, L ;
BORTOLAN, G .
BIOSYSTEMS, 1983, 16 (3-4) :297-305
[2]   Towards a blueprint of the cell cycle [J].
Alberghina, L ;
Porro, D ;
Cazzador, L .
ONCOGENE, 2001, 20 (09) :1128-1134
[3]  
ALBERGHINA L, IN PRESS J CELL BIOL
[4]  
ALBERGHINA L, 2003, 1 INT WORKSH SYST BI, P6
[5]  
ALBERGHINA L, IN PRESS SYSTEMS BIO
[6]   Robustness in bacterial chemotaxis [J].
Alon, U ;
Surette, MG ;
Barkai, N ;
Leibler, S .
NATURE, 1999, 397 (6715) :168-171
[7]   Chromosome separation and exit from mitosis in budding yeast: Dependence on growth revealed by cAMP-mediated inhibition [J].
Anghileri, P ;
Branduardi, P ;
Sternieri, F ;
Monti, P ;
Visintin, R ;
Bevilacqua, A ;
Alberghina, L ;
Martegani, E ;
Baroni, MD .
EXPERIMENTAL CELL RESEARCH, 1999, 250 (02) :510-523
[8]   Network biology:: Understanding the cell's functional organization [J].
Barabási, AL ;
Oltvai, ZN .
NATURE REVIEWS GENETICS, 2004, 5 (02) :101-U15
[9]  
BARBERIS M, UNPUB
[10]   p27Kip1 modulates cell migration through the regulation of RhoA activation [J].
Besson, A ;
Gurian-West, M ;
Schmidt, A ;
Hall, A ;
Roberts, JM .
GENES & DEVELOPMENT, 2004, 18 (08) :862-876