Identification of Novel Tumor Suppressor Genes in Human Breast Cancer Using Nonsense-Mediated mRNA Decay Inhibition (NMDI)-Microarray Analysis

Abstract

This project sought to identify genes that harbor nonsense mutations in breast cancer cell lines that are commonly used as in vitro models in the study of breast cancer biology, with the ultimate aim of identifying novel tumor suppressor genes for sporadic breast cancer. We focused our efforts on the long arm chromosome 22 which is known to undergo LOH in primary breast tumors. Before the NMD-microarray strategy could be undertaken, we very thoroughly characterized chromosome 22q copy number and allelic imbalance in several breast cancer cell lines by integrating publicly available genetic data with empirical data derived from 317K single nucleotide polymorphism (SNP) arrays. MCF-7, T-47D, and MDA-MB-231 breast cancer-derived cell lines were selected for NMD-microarray analysis. Two different regimens for inhibiting NMD were then directly compared for their ability to specifically inhibit NMD while leaving wild-type transcripts unaffected. The improved second-generation NMD protocol was performed and we eagerly await the results of the Affymetrix GeneChip expression arrays so that interrogation of the expression data may begin.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 2007
Accession Number
ADA486630

Entities

People

  • Cameron N. Johnstone

Organizations

  • University of Pennsylvania

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Colon Cancer
  • Cultured Cells
  • Dna Microarrays
  • Epithelial Cells
  • Genetic Code
  • Genetics
  • Genomic Instability
  • Microarray Analysis
  • Microsatellites
  • Neoplasms
  • Proteins
  • Rna Stability
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

  • Clinical Trial Research.
  • Molecular Biology and Genetics
  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology