Gene expression profiling, genetic networks, and cellular states: an integrating concept for tumorigenesis and drug discovery

Abstract. Genome-wide expression monitoring, a novel tool of functional genomics, is currently used mainly to identify groups of coregulated genes and to discover genes expressed differentially in distinct situations that could serve as drug targets. This descriptive approach, however, fails to extract "distributed" information embedded in the genomic regulatory network and manifested in distinct gene activation profiles. A model based on the formalism of boolean genetic networks in which cellular states are represented by attractors in a discrete dynamic system can serve as a conceptual framework for an integrative interpretation of gene expression profiles. Such a global (genome-wide) view of "gene function" in the regulation of the dynamic relationship between proliferation, differentiation, and apoptosis can provide new insights into cellular homeostasis and the origins of neoplasia. Implications for a rational approach to the identification of new drug targets for cancer treatment are discussed.

[1]  A. Novick,et al.  ENZYME INDUCTION AS AN ALL-OR-NONE PHENOMENON. , 1957, Proceedings of the National Academy of Sciences of the United States of America.

[2]  J. Monod,et al.  Teleonomic mechanisms in cellular metabolism, growth, and differentiation. , 1961, Cold Spring Harbor symposia on quantitative biology.

[3]  S. Kauffman Metabolic stability and epigenesis in randomly constructed genetic nets. , 1969, Journal of theoretical biology.

[4]  G. B. Pierce,et al.  Differentiation of malignant to benign cells. , 1971, Cancer research.

[5]  L Glass,et al.  Co-operative components, spatial localization and oscillatory cellular dynamics. , 1972, Journal of theoretical biology.

[6]  J. Monod,et al.  General Conclusions: Teleonomic Mechanisms in Cellular Metabolism, Growth, and Differentiation , 1978 .

[7]  The Strategy of Growth , 1990 .

[8]  H. Rubin On the nature of enduring modifications induced in cells and organisms. , 1990, The American journal of physiology.

[9]  M. Mitchell Waldrop,et al.  Complexity : the emerging science and the edge of order and chaos , 1992 .

[10]  C. Guillouf,et al.  Induction of p21 (WAF-1/CIP1) during differentiation. , 1994, Oncogene.

[11]  C. Winterford,et al.  Apoptosis. Its significance in cancer and cancer Therapy , 1994, Cancer.

[12]  A. Lassar,et al.  Inhibition of myogenic differentiation in proliferating myoblasts by cyclin D1-dependent kinase , 1995, Science.

[13]  G. Hannon,et al.  Correlation of terminal cell cycle arrest of skeletal muscle with induction of p21 by MyoD , 1995, Science.

[14]  G. Evan,et al.  Apoptosis and the cell cycle. , 1995, Current opinion in cell biology.

[15]  G. Hannon,et al.  Cloning and characterization of murine p16INK4a and p15INK4b genes. , 1995, Oncogene.

[16]  Lars Holmgren,et al.  Dormancy of micrometastases: Balanced proliferation and apoptosis in the presence of angiogenesis suppression , 1995, Nature Medicine.

[17]  A. Keller,et al.  Model genetic circuits encoding autoregulatory transcription factors. , 1995, Journal of theoretical biology.

[18]  D. Bray Protein molecules as computational elements in living cells , 1995, Nature.

[19]  Jonathan A. Cooper,et al.  Mitogen and stress response pathways: MAP kinase cascades and phosphatase regulation in mammals and yeast. , 1995, Current opinion in cell biology.

[20]  L. Penland,et al.  Use of a cDNA microarray to analyse gene expression patterns in human cancer , 1996, Nature Genetics.

[21]  J. Pouysségur,et al.  A temporal and biochemical link between growth factor-activated MAP kinases, cyclin D1 induction and cell cycle entry. , 1996, Progress in cell cycle research.

[22]  Elucidation of gene function using C-5 propyne antisense oligonucleotides , 1996, Nature Biotechnology.

[23]  Flanagan Wm,et al.  Elucidation of gene function using C-5 propyne antisense oligonucleotides , 1996 .

[24]  M. Macleod A possible role in chemical carcinogenesis for epigenetic, heritable changes in gene expression , 1996, Molecular carcinogenesis.

[25]  C. Sherr Cancer Cell Cycles , 1996, Science.

[26]  C. Der,et al.  Loss of oncogenic ras expression does not correlate with loss of tumorigenicity in human cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[27]  S. Schultz Homeostasis, Humpty Dumpty, and Integrative Biology , 1996 .

[28]  M. Jackson,et al.  Cloning differentially expressed mRNAs , 1996, Nature Biotechnology.

[29]  P. Brown,et al.  Parallel human genome analysis: microarray-based expression monitoring of 1000 genes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[30]  T. van Dyke,et al.  Apoptosis and cancer mechanisms. , 1997, Cancer surveys.

[31]  D. Green A Myc-Induced Apoptosis Pathway Surfaces , 1997, Science.

[32]  R H Hruban,et al.  Gene expression profiles in normal and cancer cells. , 1997, Science.

[33]  Z. Werb,et al.  Matrix Metalloproteinase Stromelysin-1 Triggers a Cascade of Molecular Alterations That Leads to Stable Epithelial-to-Mesenchymal Conversion and a Premalignant Phenotype in Mammary Epithelial Cells , 1997, The Journal of cell biology.

[34]  P. Brown,et al.  Exploring the metabolic and genetic control of gene expression on a genomic scale. , 1997, Science.

[35]  Richard C. Strohman,et al.  The coming Kuhnian revolution in biology , 1997, Nature Biotechnology.

[36]  C. Y. Wang,et al.  Requirement of NF-kappaB activation to suppress p53-independent apoptosis induced by oncogenic Ras. , 1997, Science.

[37]  M Schena,et al.  Microarrays: biotechnology's discovery platform for functional genomics. , 1998, Trends in biotechnology.

[38]  A. Arkin,et al.  Simulation of prokaryotic genetic circuits. , 1998, Annual review of biophysics and biomolecular structure.

[39]  B. Lewin The Mystique of Epigenetics , 1998, Cell.

[40]  J. Barker,et al.  Large-scale temporal gene expression mapping of central nervous system development. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[41]  J. Hodgson,et al.  DNA chips: An array of possibilities , 1998, Nature Biotechnology.

[42]  D. Sidransky,et al.  Role of the p16 tumor suppressor gene in cancer. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[43]  Araceli M. Huerta,et al.  From specific gene regulation to genomic networks: a global analysis of transcriptional regulation in Escherichia coli. , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

[44]  D. Botstein,et al.  The transcriptional program of sporulation in budding yeast. , 1998, Science.

[45]  G. Evan,et al.  A matter of life and cell death. , 1998, Science.

[46]  Michael R. Green,et al.  Dissecting the Regulatory Circuitry of a Eukaryotic Genome , 1998, Cell.

[47]  Michael Ruogu Zhang,et al.  Comprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization. , 1998, Molecular biology of the cell.

[48]  A Wuensche,et al.  Genomic regulation modeled as a network with basins of attraction. , 1998, Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing.

[49]  F. Di Cunto,et al.  Inhibitory function of p21Cip1/WAF1 in differentiation of primary mouse keratinocytes independent of cell cycle control. , 1998, Science.

[50]  D. Botstein,et al.  The transcriptional program in the response of human fibroblasts to serum. , 1999, Science.

[51]  U. Alon,et al.  Robustness in bacterial chemotaxis , 2022 .

[52]  D. Botstein,et al.  Cluster analysis and display of genome-wide expression patterns. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[53]  U. Bhalla,et al.  Emergent properties of networks of biological signaling pathways. , 1999, Science.

[54]  Jonathan Knight,et al.  When the chips are down , 2001, Nature.

[55]  Stuart A. Kauffman,et al.  ORIGINS OF ORDER , 2019, Origins of Order.