Shafaat Rabbani
Associate Member
Psychiatry
McGill University
Canada
Biography
Basic Cancer Research
Research Interest
The focus of research in my laboratory is to investigate the progression of hormone dependent malignancies (breast and prostate cancer). Toward these objectives, I am examining the role of urokinase (uPA) in the process of tumor invasion, growth and metastasis. The change in the methylation status of uPA promoter is being evaluated as the epigenetic mechanism regulating uPA gene transcription in normal, early, and late stage breast and prostate cancer. We are developing novel diagnostic and therapeutic strategies to block uPA production and its interaction with cell surface uPAR to block tumor growth and metastasis. Using our well established models of breast and prostate cancer which closely mimics the behavior of these cancers including their propensity to develop skeletal metastasis, we are examining the efficacy of small molecules, peptides, monoclonal antibodies, oligonucleotides, and gene therapy for further evaluation in patients with these common cancers. Additionally we are developing highly sensitive and reliable molecular approaches to determine the levels of uPA expression including methylation specific PCR which can predict the methylation status of uPA, invasive potential of tumor cells and response to therapy. These results will help design an effective therapeutic strategy to block uPA/uPAR interaction.
Publications
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A common promoter hypomethylation signature in invasive breast, liver and prostate cancer cell lines reveals novel targets involved in cancer invasiveness. Cheishvili D, Stefanska B, Yi C, Li CC, Yu P, Arakelian A, Tanvir I, Khan HA, Rabbani S, Szyf M.
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Erratum to: Cyclin D1 cooperates with p21 to regulate TGFβ-mediated breast cancer cell migration and tumor local invasion. Dai M, Al-Odaini AA, Fils-Aimé N, Villatoro MA, Guo J, Arakelian A, Rabbani SA, Ali S, Lebrun JJ.
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Erratum to: A novel function for p21 Cip1 and acetyltransferase p/CAF as critical transcriptional regulators of TGFβ-mediated breast cancer cell migration and invasion. Dai M, Al-Odaini AA, Arakelian A, Rabbani SA, Ali S, Lebrun JJ.