Molecular Interactions of Bcl-2 Family Members in Breast Cancer Cells.
Abstract
A major genetic event that occurs in the pathogenesis of breast carcinoma involves alterations in the Bcl-2 survival pathway. To determine the role of the Bcl-2 family in maintaining cancer cell viability, we constructed a recombinant adenovirus vector that expresses Bcl-xs, a dominant inhibitor of these proteins. In the original proposal, we proposed studies to determine the mechanism involved in Bcl-xs-mediated apoptosis, to characterize cellular proteins that interact with Bcl-xs using biochemical and genetic approaches, and to use a transgenic model of Bcl-xs expression in the breast to assess the requirement for Bcl-2/Bcl-xl in the maintenance of normal breast epithelia and tumor growth. During the last two years, we have characterized the interaction of Bcl-xs with Bcl-2 and Bcl-xl and identified through a genetic screen, HRK, a novel protein that interacts with Bcl-2 and Bcl-xl. Mutational analysis of Bcl-xs revealed a conserved region of this protein that is important for interaction with Bcl-xl and induction of apoptosis. Bcl-xl and Bcl-x2 were found to associate with Apaf- 1, a critical regulator of caspases and cell death, suggesting that Bcl-x2 might antagonize Bcl-xl through Apaf-1.
Document Details
- Document Type
- Technical Report
- Publication Date
- Sep 01, 1998
- Accession Number
- ADA358091
Entities
People
- Gabriel Nunez
Organizations
- University of Michigan