The major research focus in the Woo laboratory is to elucidate molecular mechanisms that determine pathogenesis of insulin resistance and type 2 diabetes, which are well known to increase the risk of cardiovascular disease and cancer. Our research interests include explaining mechanisms of islet apoptosis and survival in physiological and diabetic states. We are investigating many of the fundamental genes that are involved in cell survival and apoptosis, such as caspases, tumour suppressors and oncogenes. Many of these fundamental genes have essential physiological roles in metabolic tissues such as liver, muscle, adipose tissue, and the pancreatic islets. The roles of many of the fundamental genes are highly context dependent and are specific for the tissue in which they function. Using genetically engineered mice, we examine the whole body physiology as well as take biological, biochemical and molecular approaches to define physiological roles in specific tissues, in addition to defining its potential pathogenic role in diabetes. We also study the role of insulin resistance in cancer and cardiovascular diseases. These approaches to clarify tissue-specific molecular mechanisms have wide implications for better understanding and treatment of both type 1 and type 2 diabetes as well as its relationships to cancer and cardiovascular development.
J Endocr Soc. 2018 Apr 01;2(4):336-347
Dietary Curcumin Intervention Targets Mouse White Adipose Tissue Inflammation and Brown Adipose Tissue UCP1 Expression.
Obesity (Silver Spring). 2018 Feb 06;:
Trends Endocrinol Metab. 2017 Nov 27;:
Extracellular matrix-derived extracellular vesicles promote cardiomyocyte growth and electrical activity in engineered cardiac atria.
Biomaterials. 2017 Sep 04;146:49-59
Sci Rep. 2017 Aug 09;7(1):7653
JCI Insight. 2017 Jul 20;2(14):
Sci Immunol. 2017 Apr 21;2(10):
ULK1 prevents cardiac dysfunction in obesity through autophagy-meditated regulation of lipid metabolism.
Cardiovasc Res. 2017 Apr 17;:
Janus Kinase 2 Regulates Transcription Factor EB Expression and Autophagy Completion in Glomerular Podocytes.
J Am Soc Nephrol. 2017 Apr 19;:
Nat Commun. 2017 Feb 06;8:14360
Scientist, Toronto General Hospital Research Institute (TGHRI)
Professor, Departments of Medicine and Immunology and Institute of Medical Science, University of Toronto
Head, Division of Endocrinology and Metabolism
Canada Research Chair in Signal Transduction in Diabetes Pathogenesis