Systems biology of the metabolic network regulated by the Akt pathway

被引:28
作者
Mosca, Ettore [1 ]
Barcella, Matteo [1 ]
Alfieri, Roberta [1 ]
Bevilacqua, Annamaria [2 ,3 ]
Canti, Gianfranco [3 ]
Milanesi, Luciano [1 ]
机构
[1] CNR, Inst Biomed Technol, I-20090 Segrate, Mi, Italy
[2] Univ Telemat San Raffaele Roma, I-00166 Rome, Italy
[3] Univ Milan, Dept Pharmacol, I-20129 Milan, Italy
关键词
PI3K/Akt pathway; Metabolic network; Systems biology; Kinetic models; Glycolysis; Cancer; PROTEIN-KINASE-B; TRICARBOXYLIC-ACID CYCLE; COMPUTATIONAL MODEL; ENERGY-METABOLISM; CITRATE LYASE; SILICON CELL; RAT-BRAIN; CANCER; GLYCOLYSIS; PHOSPHORYLATION;
D O I
10.1016/j.biotechadv.2011.08.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cancer has been proposed as an example of systems biology disease or network disease. Accordingly, tumor cells differ from their normal counterparts more in terms of intracellular network dynamics than single markers. Here we shall focus on a recently recognized hallmark of cancer, the deregulation of cellular energetics. The constitutive activation of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway has been confirmed as an essential step toward cell transformation. We will consider how the effects of Akt activation are connected with cell metabolism; more precisely, we will review existing metabolic models and discuss the current knowledge available to construct a kinetic model of the most relevant metabolic processes regulated by the PI3K/Akt pathway. The model will enable a systems biology approach to predict the metabolic targets that may inhibit cell growth under hyper activation of Akt. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:131 / 141
页数:11
相关论文
共 93 条
[1]   Phosphoinositide 3-kinase accelerates autophagic cell death during glucose deprivation in the rat cardiomyocyte-derived cell line H9c2 [J].
Aki, T ;
Yamaguchi, K ;
Fujimiya, T ;
Mizukami, Y .
ONCOGENE, 2003, 22 (52) :8529-8535
[2]   Integrative mathematical oncology [J].
Anderson, Alexander R. A. ;
Quaranta, Vito .
NATURE REVIEWS CANCER, 2008, 8 (03) :227-234
[3]  
[Anonymous], [No title captured]
[4]  
[Anonymous], 2005, SYSTEMS BIOL DEFINIT
[5]   Bcl-2 phosphorylation and apoptosis activated by damaged microtubules require mTOR and are regulated by Akt [J].
Asnaghi, L ;
Calastretti, A ;
Bevilacqua, A ;
D'Agnano, I ;
Gatti, G ;
Canti, G ;
Delia, D ;
Capaccioli, S ;
Nicolin, A .
ONCOGENE, 2004, 23 (34) :5781-5791
[6]   Regulation of GLUT1 gene transcription by the serine threonine kinase Akt1 [J].
Barthel, A ;
Okino, ST ;
Liao, JF ;
Nakatani, K ;
Li, JP ;
Whitlock, JP ;
Roth, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (29) :20281-20286
[7]   The identification of ATP-citrate lyase as a protein kinase B (Akt) substrate in primary adipocytes [J].
Berwick, DC ;
Hers, I ;
Heesom, KJ ;
Moule, SK ;
Tavaré, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :33895-33900
[8]   Beyond the oncogene paradigm: Understanding complexity in cancerogenesis [J].
Bizzarri, M. ;
Cucina, A. ;
Conti, F. ;
D'Anselmi, F. .
ACTA BIOTHEORETICA, 2008, 56 (03) :173-196
[9]  
Boyer PD., 1962, ENZYMES, P95
[10]   The multifarious short-term regulation of ammonium assimilation of Escherichia coli:: dissection using an in silico replica [J].
Bruggeman, FJ ;
Boogerd, FC ;
Westerhoff, HV .
FEBS JOURNAL, 2005, 272 (08) :1965-1985