Beyond Genome 2008 Applying System Biology Applying System Biology RNA Interference Personal Medicine Targeting Gene Therapy
Beyond Genome 2008
2008年6月8日(日)〜11日(水) 米国、サンフランシスコ、フェアモントホテル

遺伝子標的療法


THERAPEUTIC MODALITIES
June 10-11

1日目 | 2日目

6月 11日 (水)

7:00 am - 4:00 pm Registration Open 

7:30am Facilitated Break-Out Discussion Groups & Morning Coffee

8:15 Chairperson’s Remarks

KEYNOTE PRESENTATION

8:20 From Molecular Interaction Networks to the Master Regulators of Neoplastic Phenotypes: Cancer Systems Biology Comes of Age
Andrea Califano, Ph.D., Professor, Director, Columbia National Center for Biomedical Computing, Associate Director, Herbert Irving Comprehensive Cancer Center
The identification of genes acting synergistically as master regulators of physiologic and pathologic cellular phenotypes is still an open problem in systems biology and there are no biochemi-cally validated examples for human cells. Here we apply a systems biology approach to identify the repertoire of transcription factors (TFs) that constitute the master regulation module re-sponsible for synergistic activation of a tumor-specific signature.

8:50 Statistical and Computational Pharmacogenetics: Detecting Genes for Drug Response 
Rongling Wu, Prof., University of Florida Research Foundation Professor, Statistics, University of Florida
I will present a conceptual framework for computing genes and genome for drug response by integrating mathematical and chemical aspects of drug reactions in the body. With this frame-work, specific DNA sequence variants can be identified on the basis of the test of a few parameters that define the shape and pattern of drug responses, which thus enhances the precision of parameter estimation as well as biological and clinical relevance in pharmacogenetic and pharmacogenomic research.

9:20 Clotting, Cascades, and Computers - Systems Biology in Personalized Medicine
Michael Roehrl, M.D., Ph.D., Pathology and Laboratory Medicine, Massachusetts General Hospital 
The human blood clotting system is a complex and highly regulated network of biomolecular interactions. Data from careful biochemical measurements can be integrated into quantitative and predictive computational models of blood coagulation. Millions of patients receive the oral anticoagulant Coumadin to prevent fatal thromboembolic events. Personalized Coumadin dosing is both cumbersome and expensive and potentially dangerous. Coumadin is among the top 10 drugs with the largest number of serious adverse event reports submitted to the FDA. We show how a novel Systems Biological approach can be used in the clinical setting to personalize Coumadin dosing and to achieve safe therapeutic goals. 

9:50 Networking Coffee Break, Poster and Exhibit Viewing

10:45 Identify Pathway Specific Gene Signatures for Cancer Prognosis using Gene Expression Profiling Data
Dan Li, Ph.D., Principle Research Scientist, Informatics, Integrative Biology, Eli Lilly and Company
Neoplastic transformation and progression is driven by deregulated cellular pathways that control cell fate, growth, differentiation and survival. Although significant progress has been made to identify and characterize oncogenes, tumor suppressors and the molecular pathways that they regulate, it remains largely unclear what pathways play a critical role in the development of different tumor types. Post-genomic era technology in gene expression profiling has provided a powerful tool to study gene regulations in cancers at the molecular level. In this study, we developed and applied a novel approach to derive gene signatures for cancer prognosis in the context of known biological pathways. 

11:15 Genome-wide Transcriptional Fingerprinting of Hepatotoxicity Regulatory Networks Using Multiplex Parallel High Throughput ChIP-on-Chip Assays 
Jeff Falk, Ph.D., Director, Technology Applications, Molecular Biology, Aviva Systems Biology
A genome-wide transcription factor mapping consortium is currently being assembled facilitate global identification of key toxicity and disease-related networks and biomarkers by providing reference fingerprints of transcription factor-mediated pathway modulations in key tissues that can then be compared with similar profiles derived from disease-related or therapeutic com-pound treated samples. We will describe the initial phase of experiments utilizing our next generation ChIP-on-chip technology for mapping of transcriptional networks that pinpoint critical pathways and biomarkers associated with hepatotoxicity. 

11:45 Systems Biology of Melanoma
William Kaufmann, Ph.D., Professor, Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill
I propose to describe a model of human carcinogenesis that is based upon the interaction of an external stress (sunlight) with mutations in the MAPK signaling pathway in melanocytes to cause deletions in the CDKN2A tumor suppressor locus that encodes p16INK4A and ARF. Systems biology approaches to the model include generation of genetic and physical interaction networks to model the DNA damage response, global analysis of gene expression to identify melanoma subtypes, and mathematical models of nucleotide excision repair and G2 DNA damage checkpoint responses.

12:15 pm Close of Morning Session

12:30 Luncheon Technology Workshops (Sponsorships Available) or Lunch on Your Own

1:45 Chairperson’s Remarks

1:50 A Synthetic Gene Delivery System for IL-12: From Bench to Clinic 
Khursheed Anwer, Ph.D., Vice President, Research & Development, Expression Genetics, Inc. 
This presentation describes the discovery and development of a synthetic lipopolymer for gene delivery of IL-12 for cancer. Synthesis, formulation, scale-up, stability, animal safety/toxicity, biodistribution and results from two clinical trials in ovarian cancer patients will be discussed. Application for additional cancer indications will also be described briefly.

2:20 Gene Therapy Development using HIV as a Specific Example
Geoff Symonds, Ph.D., Senior Research Director, Global Product Leader, HIV Gene Therapy, Johnson & Johnson Research 
Gene Therapy represents a different treatment paradigm and the presentation will address the development process within the setting of big Pharma using the specific example of Gene Ther-apy for HIV. Similarities and differences to small molecule and biologics development will be discussed, as well as the means by which Gene Therapy can be ‘incubated’ to a point that it can stand alone. 

2:50 Evidence of Neuroregeneration using Vascular Endothelial Growth Factor Zinc Finger Protein Activator (SB-509) in Patients with Diabetic Neuropathy: A Chronic Degenerative Polyneuropathy
Dale Ando, M.D., Vice President of Development, Chief Medical Officer, Sangamo BioSciences, Inc.
Twenty four patients were treated with either VEGF Zinc finger protein plasmid DNA(SB-509 n=12) or placebo (n=12) at a single treatment and were followed for clinical neurologic im-provement for 6 months. There was a statistically significant 25% improvement in Quantitative Sensory Testing in the lower extremities. Motor and Sensory Nerve Conduction Velocities showed a trend for improvement in a clinically relevant magnitude. This study provided the basis for two Phase 2 trials in mild to moderated and moderate to severe Diabetic Neuropathy.

3:20 Networking Refreshment Break, Last Chance for Poster and Exhibit Viewing

4:00 Poster Awards in the Exhibit Hall

PLENARY KEYNOTE PRESENTATION

My Daughter’s DNA: Networking the Dots for a Diagnosis
Hugh Young Rienhoff, Jr., M.D., Director, MyDaughtersDNA.org

Photo Credit: Cody Pickens


Collaboration Across Areas of Expertise

5:30 Close of Conference

1日目 | 2日目

言語選択:
Korean
Traditional Chinese
Simplified Chinese

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2008年6月8日(日)〜11日(水) 米国、サンフランシスコ、フェアモントホテル