Molecular Modeling of Estrogen Receptor alpha Mutated Breast Cancer to Guide New Therapeutic Strategies

Abstract

The expression of estrogen receptor alpha (ER) is assayed in every breast cancer biopsy at the time of diagnosis with the majority of tumors (~70 ) expressing ER. Hormone therapy is given to patients with ER expressing tumors for years after surgical resection to block the creation of estrogens or the activity of ER. Unfortunately, many patients develop hormone therapy resistant tumors and once metastatic disease is found in these patients, the outlook is poor with the median survival time of slightly over one year. The recent discovery of mutations in the ligand-binding domain (LBD) of ER in 10-40 of metastatic hormone therapy resistant breast tumors suggests that these mutations may be a common mechanism leading to resistance. There is a need to understand the molecular changes that arise due to ER LBD mutations and find effective treatments for patients whose tumors harbor these mutations. We have two main goals for this project. The first goal is to characterize the molecular consequences that are specific to ER LBD mutations found in metastatic breast cancer. The second goal of the project is to identify promising targeted therapies for patients with hormone therapy resistant breast tumors that harbor ER LBD mutations.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2017
Accession Number
AD1047600

Entities

People

  • Jay Gertz

Organizations

  • University of Utah

Tags

DTIC Thesaurus Topics

  • Biology
  • Biomedical Research
  • Breast Cancer
  • Cell Line
  • Cells
  • Department Of Defense
  • Diseases And Disorders
  • Estrogens
  • Health Services
  • Hormones
  • Indicator Dyes
  • Medical Personnel
  • Molecular Biology
  • Neoplasms
  • Resistance
  • Students
  • Tumor Cell Line

Fields of Study

  • Medicine

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular and genetic basis of cancer.