Associate Professor, Department of Pathology and Department of Radiation Oncology
Researcher, Department of Urology, G.V. "Sonny" Montgomery Veterans Administration Medical CenterTumor Cell Biology ProgramPhD, Biomedical Sciences, 2004, University of Chile, Santiago, ChilePostdoc, 2004-08, Loyola University Medical Center, Maywood, ILAssistant Professor, 2008-11, Mayo Clinic Cancer Center, Rochester, MN
Contact information2500 N. State St., Room G657Jackson, MS 39216Phone: (601) 815-3060E-mail: email@example.com
The general research interest focus of our lab is on modulating cellular microenvironment to offset the effects of disease and aging.
One of our projects tests the hypothesis that hypoxically grown cells mimic more closely the antigenic signature of (the naturally hypoxic) tumor cells in situ than do the currently studied cellular vaccines prepared in air. The aim is to characterize the antigenic landscape of hypoxically cultured PCa cells and compare it to that of normoxic PCa cells.
Consequently, we are identifying oxygen-tension (ρO2) responsive genes and proteins in PCa cells using transcriptomics, proteomics and immune techniques for detection of tumor-associated antigens in PCa cells. Our findings are validated by studying gene expression also in patient-derived PCa tissue.
In another project, we have found the transcripts of hypoxia-regulated genes, overexpressed in human primary PCa and human PCa cell lines. In our studies gene expression correlated with pathological scores and prognosis. Consequently, we hypothesize that hypoxia-regulated transcript levels can serve as a prognostic factor. We are testing this hypothesis by measuring the levels of hypoxia-controlled transcripts in resected PCa tissues and studying the association with survival.
In addition, in PCa cells, we are overexpressing selected genes and studying the effects of hypoxia-controlled genes on proliferation, anchorage-dependent and independent growth, and sensitivity to cytotoxic drugs. Validation of hypoxia-controlled genes' role in tumor progression will classify these molecules as a potentially new biomarkers and therapeutic targets.
Identification of molecular mechanisms of hypoxia controlled genes -mediated PCa tumorigenesis will poise us to propose them as potential therapeutic targets. Our long term goal is to identify novel therapeutic protocols for PCa and other tumors treatment. In this regard, we have developed a new focus area in colorectal cancer (CRC). We have identified hypoxia-sensitive protein markers with the ability to define a “stem-like” subtype to predict high-risk CRC in African-Americans (known to have more aggressive CRC). Identification of ethnic-specific tumor markers for CRC will set the ground for future submissions including a validation group and unraveling of the cellular and molecular underlining mechanisms. We anticipate gaining knowledge to impact CRC health disparities.
2500 North State Street
Jackson, MS 39216
General Information: 601-984-1000
Patient Appointments: 888-815-2005