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Cancer Research Society invests in ɬÀï·¬ discoveries

Published: 20 November 2025

Nine ɬÀï·¬ researchers have received funding from the Cancer Research Society (CRS) through its Operating Grants competition,.

The awarded projects address some of the most pressing challenges in oncology, from therapy resistance in brain cancers to the biology of tumor progression in breast and prostate cancers. The CRS awarded funding to 100 research projects across Canada.

The Operating Grants program is the primary means by which the CRS fulfills its mission to support fundamental and early translational research for all types of cancer.ÌýOperating Grants provide $135,000 over two years to support high-quality, peer-reviewed research projects with clear potential to advance the prevention, diagnosis, or treatment of cancer.Ìý

Recipients:

Jerome Fortin, Assistant Professor, Department of Neurology and NeurosurgeryÌý
Discovering how to change the fate of tumor cells to treat brain cancersÌý
Professor Fortin’s project seeks strategies to alter the developmental and survival pathways of tumor cells in brain cancers, with the goal of identifying new therapeutic targets for hard-to-treat brain tumors.Ìý
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Vincent Giguere, Professor, Department of BiochemistryÌý
Investigating the role of the chromatin remodeler CHD4 (NuRD) in the progression of prostate cancerÌý
Professor Giguere will examine how the chromatin remodeling factor CHD4 and the NuRD complex influence prostate cancer progression and aim to uncover mechanisms that could be targeted to slow or stop disease progression.Ìý
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Lawrence Kazak, Associate Professor, Department of Biochemistry
Defining mechanisms of obesity-accelerated breast cancer progression
Professor Kazak’s research focuses on the biological links between obesity and breast cancer aggressivity, aiming to identify molecular pathways that explain obesity-driven tumour progression.

Peter Siegel, Professor, Department of Medicine and Member, Rosalind and Morris Goodman Cancer Institute
Investigating a role for PDLIM7 in regulating autophagy during breast cancer metastasis
Professor Siegel will investigate how the protein PDLIM7, expressed in triple-negative breast cancer cells (TNBC), leads to TNBC metastasizing in the lungs and liver by regulating autophagy, a cellular survival process that helps cancer cells endure the stresses of metastasis. The aim is to identify the basis for new strategies to limit the ability of these aggressive cancer cells to spread.

NahumÌýSonenberg,ÌýDistinguished James ɬÀï·¬ Professor, Department of Biochemistry and Gilman Cheney Chair, Rosalind and Morris Goodman Cancer Institute
Targeting eIF4E-mediated dysregulated mRNA translation as a therapeutic strategy for breast cancer
Professor Sonenberg will explore a new therapeutic strategy for triple-negative breast cancer by targeting dysregulated mRNA translation, a key process that fuels tumour growth. By combining a highly selective mRNA translation inhibitor with a complementary cell-cycle inhibitor, this project aims to open the door to more effective treatment options.

,ÌýDirector of the Rosalind and Morris Goodman Cancer Institute (GCI) andÌýProfessor, Department of Microbiology and ImmunologyÌý
Targeting MFG-E8 for treatment of cancerÌý
Professor Stagg
will investigate how MFG-E8 regulates anti-tumor immunity, and assess whether it can be targeted by antibodies for anti-cancer therapy.
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Jose Teodoro, Professor, Department of BiochemistryÌý
The impact of endogenous fatty acid esters of hydroxy fatty acids in colorectal cancerÌý
Professor °Õ±ð´Ç»å´Ç°ù´Ç’s project will evaluate how endogenous lipid metabolites, fatty acid esters of hydroxy fatty acids, affect colorectal cancer development and progression, and whether they can be leveraged for therapeutic benefit.Ìý

Ian Watson, Associate Professor, Department of Biochemistry
Investigation of vesicular stomatitis virus (VSV) in the treatment of cutaneous melanoma
Professor Watson will explore the oncolytic potential of VSV as a therapeutic for cutaneous melanoma, studying its safety, tumor-targeting properties, and capacity to stimulate anti-tumor immune responses.

John White, Professor and Chair, Department of Physiology
Development and testing of novel vitamin D receptor agonist/histone deacetylase inhibitor hybrids
Professor White’s team will design and evaluate hybrid compounds that combine vitamin D receptor activation with histone deacetylase inhibition, a dual approach that may enhance anti-cancer activity and therapeutic specificity.

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