Prostate Expression Databases: Gene Expression Resources for Comparative Studies of Prostate Carcinogenesis

Abstract

This proposal aims to test the hypothesis that integrating observations derived from mouse model systems with observations from human prostate cancers will define relevant and consistent molecular alterations critical to the development and progression of prostate carcinoma. The research accomplished to date has: 1) assembled the requisite mouse models to enable the generation of tumor gene expression data; 2) produced a second-generation mouse prostate microarray that will allow for deeper profiling of mouse prostate gene expression; 3) identified a specific gene (osteopontin) commonly associated with multiple mouse prostate cancer models; 4) developed the methods/techniques that will enable precise dissection of mouse prostate epithelium; 5) expanded the Prostate Expression Database to archive microarray data; 6) determined strain-specific gene expression differences in the mouse prostate that could contribute to phenotypic differences on prostate cancer development and progression; and 7) identified developmental pathways altered in the Pten-/- prostate cancer model that could contribute to the process of carcinogenesis.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2008
Accession Number
ADA478841

Entities

People

  • Peter S Nelson

Organizations

  • Fred Hutchinson Cancer Center

Tags

DTIC Thesaurus Topics

  • Cell Movement
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Databases
  • Genetics
  • Health Services
  • Information Science
  • Medical Personnel
  • Peptide Growth Factors
  • Prostate Cancer
  • Proteins

Fields of Study

  • Biology

Readers

  • Immunology and Pathology
  • Oncology and Biomarker-Based Cancer Detection.
  • Toxicology/Environmental Toxicology