Targeted Therapy of Human Breast Cancer by 2-5A-Antisense Directed Against Telomerase RNA

Abstract

The telomerase enzyme consists of an RNA template and a reverse transcriptase which ensures replication of the termini of chromosomes. Normal somatic cells do not express telomerase and progressively lose telomeric repeat units at each cell division which ultimately results in celluarl senescence. Rapidly growing tumor cells overcome this handicap by reexpressiong the telomerase enzyme making it a potential target for therapy. We have demonstrated using anti sense oligonuclotides that targeting the RNA component of telomerase (hTR) for degradation commits tumor cells to rapid apoptosis in vitro and in vivo. Normal cells are unaffected a tumor cells treated with oligonucleotides carrying mismatched bases do not illicit this response. The same apoptotic response was induced in breast cancer cells in vitro using small interfering RNA molecules (siRNA) targeting hTR. In these approaches only a single treatment over a seven day period was sufficient to reduce cell viability significantly. This is in contrast to the need for daily administration of the antisense molecules. These observations provide strong support for the possibility that targeting the telomerase RNA could be developed as a rational therapeutic approach if limitations of delivery and specificity can be overcome.

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Document Details

Document Type
Technical Report
Publication Date
Dec 01, 2003
Accession Number
ADA424078

Entities

People

  • John K. Cowell

Organizations

  • Health Research, Incorporated

Tags

DTIC Thesaurus Topics

  • Antisense Elements (Genetics)
  • Apoptosis
  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Contrast
  • Degradation
  • Gene Expression
  • Medical Personnel
  • Molecules
  • Neoplasms
  • Observation
  • Targeting
  • Targets
  • Tumor Cell Line
  • Viability

Fields of Study

  • Biology

Readers

  • Housing Policy Studies in Military Families with Privatization and Telomerase Allowance Units, Multi-Family Housing, and Telomere Lengths.
  • Molecular Genetics
  • Oncology (Cancer Research).