The Role of Sphingolipid- and Cholesterol-Rich Membrane Domains in Pathophsiology of Cultured Human Breast Cancer
Abstract
UPAR (urokinase-type plasminogen activator receptor) is a key player in metastasis of breast cancer cells. We suggest that uPAR, because it is a GPI-anchored protein, must be present in discrete "rafts" in the cell surface to function. Our proposal has two parts. First, we will set up systems in our lab for studying signaling trough uPAR in cultured human breast cancer cells. Second, we will disrupt rafts, and determine whether signal transduction is affected. Our most important advance this year has been in developing new tools for raft disruption. These include sterol analogs such as androstanol and coprostanol. Replacing cholesterol with these analogs allows us to disrupt rafts without depleting total cellular sterol, allowing raft disruption without the other pleiotropic effects that accompany bulk sterol removal. This will be an important tool in later experiments to examine the effect of raft disruption on uPAR-Mediated signaling and cell motility. We anticipate in the next year, we will develop improved methods for detecting uPAR in rafts in cells. We will then determine how the localization of uPAR in rafts governs its deadly activity in metastasis.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jun 01, 2003
- Accession Number
- ADA421916
Entities
People
- Deborah A. Brown
Organizations
- State University of New York