The Characterization and Treatment of Aggressive Breast Cancer

Abstract

Several groups have demonstrated that women with BRCA1 germline mutations are more likely to have breast cancers that are basal-like by gene expression profiling. While BRCA1 germline mutations are uncommon and contribute to fewer than 5% of breast cancers our lab has demonstrated that methylation occurs in up to 50% of high-grade hormone receptor negative sporadic tumors. As promoter methylation leads to transcriptional repression we propose that such tumors will be sensitive to DNA damaging agents and resistant to microtubule inhibitors given the role that BRCA1 plays in both DNA repair and cell cycle. Using the alamar blue cytotoxicity assay and five breast cancer cell lines my laboratory has demonstrated that one of two BRCA1 methylated cell lines is significantly more sensitive to cisplatin and more resistant to paclitaxel as compared to other human breast cancer cell lines with normal BRCA1 expression. These findings are currently being translated into a clinical trial where the BRCA1 methylation status of a patient's tumor will be correlated to response of the tumor to platinum-based therapy.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2007
Accession Number
ADA470889

Entities

People

  • Rita Nanda

Organizations

  • University of Chicago

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cardiovascular Physiological Phenomena
  • Cardiovascular System
  • Cell Physiological Processes
  • Data Storage Systems
  • Health Services
  • Medical Personnel
  • Myocardial Ischemia
  • Pain

Fields of Study

  • Biology

Readers

  • Molecular and genetic basis of cancer.
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology