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Launched in 2024, the New Faculty Start Up funding program offers competitive start-up packages, complementing those provided by faculties, to attract researchers of the highest caliber for tenure-track positions related to D2R. As part of this program, Ï㽶ÊÓƵ and Université de Sherbrooke will establish new tenure-track positions reserved for newly hired faculty whose primary research focus aligns with D2R. Recruitment for these positions is expected to take place from 2024 through to 2028.
The following new faculty are a result of the program's efforts so far. Recruitment of new faculty follows standard procedures for tenure-track positions, incorporating best practices in Equity, Diversity, and Inclusion. Recruitment is led by the relevant Dean in close collaboration with D2R’s Research Steering Committee.
Université de Sherbrooke |
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Taha Azad |
Karine Choquet |
Mathieu Quesnel-Vallières |
Université de Sherbrooke
Taha Azad
Using Synthetic Biology Approaches to Develop Novel Ï㽶ÊÓƵ Anti-Cancer Therapeutics
Academic Title: Assistant Professor
Hiring department and faculty: Microbiology and Infectious Diseases, Faculty of Medicine and Health Sciences
Award start date: August, 2024
D2R Foundational Axes: Ï㽶ÊÓƵ Therapeutics (Axis 2), Bioprocessing, Biomanufacturing, and Nanotechnology (Axis 3)
Our research aims to revolutionize cancer treatment using self-amplifying Ï㽶ÊÓƵ (saÏ㽶ÊÓƵ) therapeutics. These unique Ï㽶ÊÓƵ molecules replicate within cells, enhancing the expression of therapeutic proteins and potentially reducing treatment costs and frequency. We have curated a diverse library of saÏ㽶ÊÓƵs from nature and engineered them to target cancers. By characterizing saÏ㽶ÊÓƵ behavior in various cancer cells and optimizing their interaction with immune pathways, we aim to develop highly effective and personalized saÏ㽶ÊÓƵ-based treatments. Our innovative approach promises to advance Ï㽶ÊÓƵ therapeutics, providing new hope for cancer patients.
Karine Choquet
Improving disease prognosis and treatment by elucidating pre-mÏ㽶ÊÓƵ splicing dynamics
Academic Title: Assistant Professor
Hiring department and faculty: Biochemistry and Functional Genomics, Faculty of Medicine and Health Sciences
D2R award start date: August, 2024
D2R Foundational Axes: Ï㽶ÊÓƵ Therapeutics (Axis 2), Population Studies and Genomic Medicine (Axis 1), Data Science, Bioinformatics, and Computing in Personalized Medicine (Axis 5)
Premature messenger Ï㽶ÊÓƵs (pre-mÏ㽶ÊÓƵ) must undergo a process called splicing to become the mature messenger Ï㽶ÊÓƵs that are used to produce proteins, which are the building blocks of the cell. Splicing defects contribute to many human diseases. Splicing can also be modified to treat genetic diseases. Human pre-mÏ㽶ÊÓƵs are very long, but splicing has only been studied for one short section of a pre-mÏ㽶ÊÓƵ at a time. My program will investigate how splicing of different parts of a pre-mÏ㽶ÊÓƵ is connected and how this impacts the consequences of genetic mutations and the efficiency of splicing-based therapies for rare muscle diseases.
Mathieu Quesnel-Vallières
Ï㽶ÊÓƵ splicing as an oncogenic factor and as a therapeutic target
Academic Title: Assistant Professor
Hiring department and faculty: Immunology and Cell Biology, Faculty of Medicine and Health Sciences
D2R award start date: August, 2024
D2R Foundational Axes: Clinical Research, Acceleration, and Implementation (Axis 4), Ï㽶ÊÓƵ Therapeutics (Axis 2), Data Science, Bioinformatics, and Computing in Personalized Medicine (Axis 5)
Immunotherapy is new form of therapy that consists in activating the patient’s own immune system against their cancer. The tremendous potential of this new type of cancer therapy has recently been demonstrated in the clinic, but not all patients respond and some cancer types lack good targets to develop new immunotherapy. Our research uses DNA and Ï㽶ÊÓƵ sequencing methods with computational and experimental analyses to identify the molecular differences that exist between cancer and normal cells and leverage these differences to teach immune cells how to recognize and kill cancer.