Control of Transformation and Invasiveness of Breast Cancer Cells by Estrogen Regulation of Proteinase Inhibitor 9

Abstract

Thrombosis, or the abnormal clotting of the blood, is the leading cause of death in breast cancer patients. Thrombus formation is triggered factor Vlla from circulating blood encounters tissue factor (TF) on the surface of a cell, including many breast cancer cells and tumor-associated cells. It is important, therefore, to increase our understanding of the mechanisms by which TF activates the clotting cascade in breast cancer. The blood protein, antithrombin (AT), has long been thought to be the most important natural anticoagulant that targets steps of the clotting cascade downstream from TF:Vlla, but more recent work has suggested that AT can also inactivate factor Vlla bound to TF. Goals of this project included determining if AT can efficiently inhibit TF:Vlla complexes and if resulting factor Vlla-antithrombin (VIla-AT) complexes can be detected in blood. The project was successful in determining that the TF:Vlla complex can efficiently be inactivated by AT, and furthermore was successful in quantifying Vlla-AT levels in blood.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2005
Accession Number
ADA471083

Entities

People

  • Francesca C. Antonaci

Organizations

  • University of Illinois Urbana–Champaign

Tags

DTIC Thesaurus Topics

  • Anticoagulants
  • Biomedical Research
  • Blood Coagulation
  • Blood Coagulation Factors
  • Blood Proteins
  • Breast Cancer
  • Cells
  • Illinois
  • Inhibition
  • Inhibitors
  • Neoplasms
  • Proteins
  • Thrombosis
  • United States
  • Universities

Fields of Study

  • Biology
  • Medicine

Readers

  • Cardiovascular Physiology
  • Molecular Biology and Genetics
  • Oncology and Biomarker-Based Cancer Detection.