TY - JOUR
T1 - Computational systems bioinformatics and bioimaging for pathway analysis and drug screening
AU - Zhou, Xiaobo
AU - Wong, Stephen T.C.
N1 - Funding Information:
Manuscript received July 24, 2007; revised January 3, 2008. This work was supported by the Bioinformatics Program, Harvard Neurodiscovery Center (previously the Harvard Center for Neurodegeneration and Repair), Harvard Medical School, Boston, MA, under a grant and the Bioinformatics Program, The Methodist Hospital Research Institute, Weill Cornell Medical College of Cornell University, New York. The work of S. T. C. Wong was supported by the National Institutes of Health under Research Grants R01 LM008696 and R01 LM009161. The authors are with the Bioinformatics Program and Department of Radiology, The Methodist Hospital Research Institute, Weill Medical College of Cornell University, Houston, TX 77030 USA (e-mail: [email protected]).
PY - 2008/8
Y1 - 2008/8
N2 - The premise of today's drug development is that the mechanism of a disease is highly dependent upon underlying signaling and cellular pathways. Such pathways are often composed of complexes of physically interacting genes, proteins, or biochemical activities coordinated by metabolic intermediates, ions, and other small solutes and are investigated with molecular biology approaches in genomics, proteomics, and metabonomics. Nevertheless, the recent declines in the pharmaceutical industry's revenues indicate such approaches alone may not be adequate in creating successful new drugs. Our observation is that combining methods of genomics, proteomics, and metabonomics with techniques of bioimaging will systematically provide powerful means to decode or better understand molecular interactions and pathways that lead to disease and potentially generate new insights and indications for drug targets. The former methods provide the profiles of genes, proteins, and metabolites, whereas the latter techniques generate objective, quantitative phenotypes correlating to the molecular profiles and interactions. In this paper, we describe pathway reconstruction and target validation based on the proposed systems biologic approach and show selected application examples for pathway analysis and drug screening.
AB - The premise of today's drug development is that the mechanism of a disease is highly dependent upon underlying signaling and cellular pathways. Such pathways are often composed of complexes of physically interacting genes, proteins, or biochemical activities coordinated by metabolic intermediates, ions, and other small solutes and are investigated with molecular biology approaches in genomics, proteomics, and metabonomics. Nevertheless, the recent declines in the pharmaceutical industry's revenues indicate such approaches alone may not be adequate in creating successful new drugs. Our observation is that combining methods of genomics, proteomics, and metabonomics with techniques of bioimaging will systematically provide powerful means to decode or better understand molecular interactions and pathways that lead to disease and potentially generate new insights and indications for drug targets. The former methods provide the profiles of genes, proteins, and metabolites, whereas the latter techniques generate objective, quantitative phenotypes correlating to the molecular profiles and interactions. In this paper, we describe pathway reconstruction and target validation based on the proposed systems biologic approach and show selected application examples for pathway analysis and drug screening.
KW - Biomarker discovery
KW - Drug discovery
KW - High-content screen
KW - High-throughput screen
KW - RNAi
KW - System bioinformatics and bioimaging
KW - Target validation
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U2 - 10.1109/JPROC.2008.925440
DO - 10.1109/JPROC.2008.925440
M3 - Article
AN - SCOPUS:47949110106
SN - 0018-9219
VL - 96
SP - 1310
EP - 1331
JO - Proceedings of the IEEE
JF - Proceedings of the IEEE
IS - 8
M1 - 4567423
ER -