March 2005 Inside this issue... New Research Fruit flies and cancer research New treatment for depression Personalized cancer therapy Breaking News CIHR makes funding announcement Updates New venture discussed in Shanghai Visit us at... UHN's Research Internet Site |
New Research Breakthroughs at UHN
Using a genetic screening method in fruit flies, they discovered that DJ-1 prevents the tumour suppressor molecule PTEN from doing its job. With PTEN out of commission, cell growth can rage out of control and cancer can develop. Human breast and lung cancer cells also have high levels of the molecule, and lung cancer patients with high levels of DJ-1 are more likely to suffer a relapse. Says Dr. Mak, Our results suggest that DJ-1 does play a role in the development of cancer, and in the future, it may represent a valuable new target for cancer therapy. Cancer Cell. 2005 Mar;7(3): 263-273. [PubMed abstract] Funded by the Canadian Cancer Society, the National Cancer Institute of Canada, and the Canadian Institutes of Health Research Institutes: AMDI/OCI/PMH, The Campbell Family Institute for Breast Cancer Research, OCI/PMH Division: Cell & Molecular Biology
Based on the team’s previous findings that an area of the brain called Cg25 is important for mood regulation, the research team suspected that DBS might be useful to retune this area of the brain. The treatment was successful: changes observed in four of the six patients treated resembled changes that are seen when patients respond successfully to the standard treatment. Says Dr. Lozano, Our study shows that DBS can lead to striking and sustained remission of depression in some patients. It further suggests that DBS may become a standard therapy for treating severely depressed people who are resistant to drug therapy. Neuron. 2005 Mar 3;45(5):651-60. [PubMed abstract] Funded by the National Alliance for Research in Schizophrenia and Depression (NARSAD) Institute: TWRI/TWH Division: Applied & Interventional Research
Previous research by the group revealed that this genetic defect causes a protein called FGFR3 to run wild and contribute to the development of MM. In the current study, the team used special labeling techniques to reliably detect the FGFR3 protein in MM cells. They found that 98% of the time, the presence of the protein could predict the presence of the genetic defect. Patients with the defect experienced reduced overall survival. Says Dr. Chang, Our study proves that using this new technique to assess MM cells is clinically useful for identifying those MM patients who are at higher risk, a finding which will be useful for assessing treatment options for patients. Blood. 2005 Mar 10 [PubMed abstract] Funded in part by the Leukemia Research Fund of Canada Institute: TGRI/TGH Division: Experimental Therapeutics
UHN researchers received over $8M to fund 18 new research projects.
Says Dr. Paige, I’m impressed with the potential of building a partnership with the IHS. It offers the opportunity to forge further relationships with other allied Chinese Academies. This initiative is part of the larger UHN Global Ventures strategy. Delegates from the institute have been invited to visit UHN in April.
Published in the New England Journal of Medicine, the study marks the first advance in treating glioblastoma in 30 years. |
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