Complementation Screening in Mammalian Cells: Application to Cell Immortalization

Abstract

The broad goals of the work supported by this grant are twofold. The first is to develop and deploy a facile system for complementation screening in cultured mammalian cells. The second is to understand elements of cellular mortality control. With regard to the first, we have developed and deployed the MaRX system. MaRX is a retroviral vector that is specifically designed to facilitate the delivery and recovery of complex gene libraries. Thus far, we have used this system to identify genes that regulate telomerase, to elucidate potential mechanisms of TGF-b-resistance in human breast tumors, to isolate genes that confer resistance to oncogene- induced apoptosis, to find cDNAs that allow bypass of p53-induced growth arrest and to address the reversibility of immortalization processes in murine and human cells. With regard to the second broad goal, we have demonstrated that an oncogene, c-myc, can regulate telomerase activity in normal human cells Efforts over the past year have been aimed at understanding the relevance of telomerase in the immortalization of multiple cell types, at understanding the relationship between myc and telomerase activity in multiple cell types and at developing model systems in which the role of myc in cellular transformation can be addressed.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1999
Accession Number
ADA384034

Entities

People

  • Gregory Hannon

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cancer
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Genetic Structures
  • Genetics
  • Health Services
  • Lymphocytes
  • Programmed Cell Death

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Distributed Systems and Data Platform Development
  • Oncology and Biomarker-Based Cancer Detection.