Estrogen Responsive Breast Cancer Growth Regulation.

Abstract

The overall goal of this program was to characterize the serum factor(s) which regulated steroid hormone dependent human breast cancer cell growth. This included an identification of the molecule(s) and studies to establish the endocrine physiology of the regulator(s) as well as partial characterization of the receptors mediating serum factor action. We have discovered that two plasma glycoproteins, SHBG Type II and CBG, are negative regulators (i. e. inhibitors) of estrogen receptor positive (ER+) and progesterone receptor positive (PR+) breast cancer cell growth, respectively, and that autonomous (ER- and PR-) breast cancer cells are not inhibited by these glycoproteins. The new form of sex hormone binding globulin has been designated SHBG Type II. It has not previously been identified or characterized from any source. The discovery of a new regulatory role for CBG in breast cancer growth may provide our first molecular link between increased stress and an elevated risk of breast cancer.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1996
Accession Number
ADA321776

Entities

People

  • David A. Sirbasku

Organizations

  • University of Texas Health Science Center at Houston

Tags

DTIC Thesaurus Topics

  • Biological Factors
  • Biomedical And Dental Materials
  • Blood Proteins
  • Breast Cancer
  • Carrier Proteins
  • Cells
  • Chemistry
  • Immune Serums
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Polymeric Films
  • Protein Sequence Analysis
  • Proteins
  • Proteomics
  • Sex Hormones
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

  • Molecular and Cellular Biochemistry
  • Oncology (Cancer Research).