Tumor-Stromal Interactions Influence Radiation Sensitivity in Epithelial- versus Mesenchymal-Like Prostate Cancer Cells
Abstract
HS-27a human bone stromal cells, in 2D or 3D coultures, induced cellular plasticity in human prostate cancerARCaPEandARCaPMcells in an EMT model. CoculturedARCaPEorARCaPMcells with HS-27a, developed increased colony forming capacity and growth advantage, withARCaPEexhibiting the most significant increases in presence of bone or prostate stroma cells. Prostate (Pt-N or Pt-C) or bone (HS-27a) stromal cells induced significant resistance to radiation treatment inARCaPEcells compared toARCaPMcells. However pretreatment with anti-E-cadherin antibody (SHEP8-7) or anti-alpha v integrin blocking antibody (CNT095) significantly decreased stromal cell-induced radiation resistance in bothARCaPE- andARCaPM-cocultured cells. Taken together the data suggest that mesenchymal-like cancer cells reverting to epithelial-like cells in the bone microenvironment through interaction with bone marrow stromal cells and reexpress E-cadherin. These cell adhesion molecules such as E-cadherin and integrin alpha v in cancer cells induce cell survival signals and mediate resistance to cancer treatments such as radiation.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jan 01, 2010
- Source ID
- 10.1155/2010/232831
Entities
People
- Clayton Yates
- Leland W. K. Chung
- Murali Gururajan
- Peter A S Johnstone
- Ritu Aneja
- Ruoxiang Wang
- Sajni Josson
- Shian-ying Sung
- Starlette Sharp
- Timothy Turner
Organizations
- Cedars-Sinai Medical Center
- Emory University School of Medicine
- Georgia State University
- Tuskegee University
- United States Department of Defense