Tamra Erin Ogilvie
Professor
Positions
- Professor
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Department of Pediatrics
Section of Hematology-Oncology
ÌÇÐÄÊÓƵ of Medicine
Houston, Texas
- Member
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Dan L Duncan Comprehensive Cancer Center
Education
- Postdoctoral Fellowship at McMaster University
- Hamilton, Ontario, Canada
- PhD from McGill University
- Montreal, Quebec, Canada
- BSc from Western University
- London, Ontario, Canada
Professional Statement
Dr. Tamra Ogilvie's laboratory is entirely dedicated to studying medulloblastoma (MB), the most common malignant primary pediatric brain tumor. The lab has made significant contributions to the underlying cellular and molecular mechanisms regulating MB stem cell fate decisions. This includes identification of MB cells of origin (Nature, 2022), central regulators of MB self-renewal (ie. Nature Cell Biology, 2024; Nature, 2022; Nature Communications, 2020, Molecular Oncology, 2018) and potential diagnostic biomarkers for different MB molecular subgroups (i.e., Cancer Research, 2018).
Dr. Ogilvie's lab utilizes biologically relevant mouse xenograft models where human MB cells are implanted into the cerebellum to assess the effects of gain/loss of gene function as well as small molecule inhibitors as potential therapeutics (Cancer Research, 2018, Molecular Oncology, 2018, Communications Biology, 2022, Cell Death Discovery, 2023). Combining multi-omics technologies such as ChIP sequencing, RNA sequencing, single cell RNA sequencing, TurboID and digital spatial profiling of brain tumor tissue with functional assessments both in vitro and in vivo, Dr. Ogilvie has built a highly innovative research program in neuro-oncology and human stem cells.
Dr. Ogilvie's work integrates basic and preclinical studies and is currently divided into 2 major research areas: 1) Novel regulators of Group 3 MB cell fate and 2) New therapeutic strategies for SHH MB tumors. Throughout her career, she has been continuously supported by national and international funding agencies, including grants from the Canada Research Chairs program, CIHR, NSERC, the Brain Tumor Foundation of Canada, as well as the Rally Foundation for Childhood Cancer Research and Alex’s Lemonade Stand Foundation.
Dr. Ogilvie's lab utilizes biologically relevant mouse xenograft models where human MB cells are implanted into the cerebellum to assess the effects of gain/loss of gene function as well as small molecule inhibitors as potential therapeutics (Cancer Research, 2018, Molecular Oncology, 2018, Communications Biology, 2022, Cell Death Discovery, 2023). Combining multi-omics technologies such as ChIP sequencing, RNA sequencing, single cell RNA sequencing, TurboID and digital spatial profiling of brain tumor tissue with functional assessments both in vitro and in vivo, Dr. Ogilvie has built a highly innovative research program in neuro-oncology and human stem cells.
Dr. Ogilvie's work integrates basic and preclinical studies and is currently divided into 2 major research areas: 1) Novel regulators of Group 3 MB cell fate and 2) New therapeutic strategies for SHH MB tumors. Throughout her career, she has been continuously supported by national and international funding agencies, including grants from the Canada Research Chairs program, CIHR, NSERC, the Brain Tumor Foundation of Canada, as well as the Rally Foundation for Childhood Cancer Research and Alex’s Lemonade Stand Foundation.
Websites
Selected Publications
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Saulnier O, Zagozewski J, Liang L, Hendrikse LD, Layug P, Gordon V, Aldinger KA, Haldipur P, Borlase S, Coudière-Morrison L, Cai T, Martell E, Gonzales NM, Palidwor G, Porter CJ, Richard S, Sharif T, Millen KJ, Doble BW, Taylor MD, Werbowetski-Ogilvie TE.. " " Nat Cell Biol. 2024 ;
Pubmed PMID: . -
Borlase S, DeCarlo A, Morrison LC, Liang L, Porter CJ, Ramaswamy V, Werbowetski-Ogilvie TE.. " " Cell Death Discov. 2023 ;
Pubmed PMID: . -
Hendrikse LD, Haldipur P, Saulnier O, […] Doble, BW, Werbowetski-Ogilvie TE*, Millen K*, Suzuki H*, Taylor MD*.. " " Nature. 2022 ;
Pubmed PMID: . -
Zagozewski J, Borlase S, Guppy BJ, Coudière-Morrison L, Shahriary GM, Gordon V, Liang L, Cheng S, Porter CJ, Kelley R, Hawkins C, Chan JA, Liang Y, Gong J, Nör C, Saulnier O, Wechsler-Reya RJ, Ramaswamy V, Werbowetski-Ogilvie TE.. " " Commun Biol. 2022 ;
Pubmed PMID: .
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