May 2005 Inside this issue... New Research Hereditary Hep C Heralds Promising Parkinson Protector Hormone-Immune Harmony Destructive Deed in Diabetes Development Disclosed New Faces in Research Kudos for Koch Breaking News Champion Chairs Visit us at... UHN's Research Internet Site |
New Research Breakthroughs at UHN
![]() The research team used advanced genomics techniques and microarray technology to identify a subset of 18 genes that can predict a patient’s response to therapy. The study followed 31 patients with the disease who were treated at TWRI/TWH. Says Dr. McGilvray, Our results show that a small number of genes can predict how a patient will respond to therapy, and it suggests that these genes may be important for helping the patient eliminate the virus. In the future we might be able to manipulate the products of these genes to improve how patients respond to treatment. Gastroenterology 2005 May; 128(5):1437-44. [PubMed abstract] Funded by the PSI Foundation and the Canadian Institutes of Health Research Institutes: TGRI/TGH and TWRI/TWH Division: Experimental Therapeutics
![]() Says Dr. Lozano, Our work suggests that DJ-1 acts to maintain the survival and health of the brain’s dopaminergic neurons. PNAS USA 2005 Apr 5;102(14):5215-20 [PubMed abstract] Research supported by the Canadian Institutes of Health Research, the Parkinson’s Society of Canada, the Parkinson’s Disease Foundation, the Michael J. Fox Foundation, and the Canadian Stroke Network. Institute: TWRI/TWH and AMDI/OCI/PMH Division: Applied & Interventional Research and Stem Cell & Developmental Biology
The researchers found that a gene called Ikaros is key for the development of both systems. They found that neither the immune nor the hormonal system functioned properly in mice missing Ikaros, and mice missing the gene had a reduced chance of survival. Says Dr. Asa, If this finding holds true in humans, it could help identify people at risk of developing disesases characterized by abnormal immune surveillance including inflammatory diseases and cancers. J Clin Invest. 2005 Apr;115(4):1021-9 [PubMed abstract] Funded by the Canadian Institutes of Health Research and the Toronto Medical Laboratories Institute: OCI/PMH Division: Applied Molecular Oncology
Type I diabetes is an autoimmune disease due to death of insulin-producing beta-cells in the pancreas. The research team studied mice genetically engineered to lack caspase-3, a molecule involved in programmed cell death. ![]() Says Dr. Woo, Mice lacking caspase-3 failed to develop diabetes, and importantly we found no evidence of an autoimmune response in their pancreatic tissues, which is a requisite step for triggering the disease. This tells us that caspase-3 is critical for the initiation of autoimmune diabetes, and our findings may have implications for preventing the onset of diabetes in the future. Mol Cell Biol. 2005 May;25(9):3620-9. [PubMed abstract] Research supported by the Canadian Institutes of Health Research, the Banting and Best Diabetes Centre, and Bickell’s Foundation. Institute: OCI/PMH and TWRI/TWH Division: Signaling Biology
Scientist, Division of Signaling Biology, OCI/PMH
![]() As a clinician-scientist, Dr. Koch spends 80% of her time in the lab, where she researches ways to manipulate the DNA repair process in cancer cells. Using proteomic techniques, she is identifying novel DNA repair components and examining their role(s) in the radiation response in human cells. She says, By exploiting the differences in DNA repair pathways in normal and cancerous cells, new targets for cancer treatment will be realized, which can also be used in combination with radiation therapy to improve treatment outcomes.
Tier I CRCs are awarded to experienced investigators recognized internationally for their achievements. Dr. Lozano’s research program will focus on identifying neurons and brain circuits involved in certain neurological disorders, and Dr. Siminovitch’s research program will focus on defining the molecular mechanisms associated with autoimmune disease. |
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