Peter Siegel, PhD

Primary Axis: 
Cancer
Secondary Axis: 
Musculoskeletal Disorders
Research Focus: 

Research focuses on defining the molecular mechanisms that control the ability of breast cancer cells to spread or "metastasize" to bone and soft tissues. He employs in vivo models for the selection of highly metastatic tumor cell populations which are then subjected to gene expression profiling to identify genes that are associated with the metastatic phenotype. Dr. Siegal is also interested in defining the importance of processes that control epithelial plasticity (epithelial to mesenchymal transitions) and the molecular mediators that contribute to the ability of cancer cells to become locally invasive and that promote breast cancer metastasis. He will employ in vivo imaging methods to track EMT in mice and to facilitate the isolation of breast cancer cells at different stages of the metastatic cascade.

Keywords: 
Breast cancer, metastasis, EMT, gene expression profiling, transgenic mice, xenograft models, TGF-beta, ErbB-2/Neu, in vivo imaging
Location: 
Rosalind and Morris Goodman Cancer Research Centre
Publications:
Guo Y, Tiedmann K, Abou Khalil J, Russo C, Siegel PM, Komarova SV. Osteoclast precursors acquire sensitivity to breast cancer derived factors early in differentiation. Bone (In press) 2008.
Northey JJ, Chmielecki J, Ngan E, Russo C, Annis MG, Muller WJ, Siegel PM. Signaling through ShcA is required for TGF-β and Neu/ErbB-2 induced breast cancer cell motility and invasion. Mol Cell Biol 28(10): 3162-3176; 2008.
Rose AAN, Pepin F, Russo C, Abou Khalil JE, Hallett M, Siegel PM. Osteoactivin promotes breast cancer metastasis to bone. Mol Cancer Res 5(10): 1001-1014; 2007.