Dr. Nicolas Bisson holds the Canada Research Chair in Proteomics of Cancer. He is an associate professor in the Department of Molecular Biology, Medical Biochemistry and Pathology of the School of Medicine at Laval University, and a regular researcher at the CHU Research Center of Québec – Laval University. He is also a member of the Laval University Cancer Research Center and the Quebec Network for Research on Protein Function, Engineering, and Applications (PROTEO). Dr. Bisson’s work aims to decipher how cells communicate with each other, and how these signaling mechanisms are deregulated in the development of cancers, particularly in the breast and prostate. In the longer term, the goal of his work is to use entire signaling networks as predictive and therapeutic tools for these cancers, in cases for which conventional strategies fail.
Communication between the cells that form the tissues of our body is of paramount importance. This dialogue is required, not only to ensure that all body parts develop normally as a result of conception, but also that they function properly throughout our lives. Deregulation of cells to send, receive or correctly assimilate signals from their environment (or other cells) can lead to diseases such as cancer. The cellular actors who assume these tasks are the proteins. Most proteins do not work alone: they combine in pairs, or in small (complexes) or large groups (networks). Dr. Bisson’s team is particularly interested in a group of proteins, called adapters, whose primary function is to associate with different proteins (and with each other) in order to help the cell integrate signals from outside and respond adequately. More particularly, they study the signals received by a family of receptors called tyrosine kinase. Through their work, they aim to identify which cell proteins associate with adapters to form complexes and networks, as well as the mechanisms used by the cell to regulate this non-random process. In addition, they aim to analyze how the composition of complexes varies when the cell receives different signals through tyrosine kinase receptors. Finally, they want to determine if the large protein networks are modified in breast and prostate cancer cells, identify what these changes are, and figure out how it is possible to return them to a normal state. To achieve these goals, the team uses innovative proteomics tools to separate and quantify proteins, cell imaging to observe them, animal models of breast or prostate cancer, and patient samples. Their work will provide new insights into protein networks that are essential to cell communication and life, and how they can be used as prognostic tools or therapeutic targets for the treatment of breast and prostate cancer.
Dr. Bisson’s work is funded by the Canadian Institutes of Health Research, the Natural Sciences and Engineering Research Council of Canada, and the Canada Foundation for Innovation.
9, rue McMahon
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- Chartier, FrançoisEmployeeL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16950+1 418-691-5439francois.chartier.1@ulaval.cafrancois.chartier@crchudequebec.ulaval.ca
9, rue McMahon
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Québec, Québec
Canada G1R 2J6 - Kreyder, Arthur RuyMaster studentL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16939+1 418-525-4444, extension 16950arthur-ruy.kreyder@crchudequebec.ulaval.ca
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Québec, QC
Canada G1R 3S3 - Lessard, FrédéricEmployeeL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16930+1 418-525-4444, extension 16939+1 418-691-5439frederic.lessard@crchudequebec.ulaval.ca
9 rue McMahon
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Canada G1R 3S3 - Osornio, Ana IsabelDoctoral studentL'Hôtel-Dieu de Québec
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Canada G1R 3S3L'Hôtel-Dieu de Québec+1 418-525-4444, extension 16939+1 418-525-4444, extension 16950ana-isabel.osornio-hernandez.1@ulaval.caana-isabel.osornio@crchudequebec.ulaval.ca
9, Rue Mcmahon
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Canada G1R 3S3 - Soham Dibyachintan, Soham DibyachintanMaster student
- St-Onge, GabrielleMaster student+1 418-525-4444, extension 16950gabrielle.st-onge@crchudequebec.ulaval.ca
- Teyssier, ValentineDoctoral studentL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16939+1 418-525-4444, extension 16950valentine.teyssier@crchudequebec.ulaval.ca
9 Rue Mcmahon
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Canada G1R 3S3 - Zhuravel, BohdanMaster studentL'Hôtel-Dieu de Québec+1 418-525-4444, extension 16950bohdan.zhuravel@crchudequebec.ulaval.ca
9 rue McMahon
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Québec, QC
Canada G1R 3S3
A Multipronged Unbiased Strategy Guides the Development of an Anti-EGFR/EPHA2-Bispecific Antibody for Combination Cancer Therapy
Journal ArticleClin Cancer Res, 29 (14), 2023.
Integration of cancer-related genetic landscape of Eph receptors and ephrins with proteomics identifies a crosstalk between EPHB6 and EGFR
Journal ArticleCell Rep, 42 (7), 2023.
Complementary Nck1/2 Signaling in Podocytes Controls α Actinin-4-Mediated Actin Organization, Adhesion, and Basement Membrane Composition
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EPH receptor tyrosine kinases phosphorylate the PAR-3 scaffold protein to modulate downstream signaling networks
Journal ArticleCell Rep, 40 (1), 2022.
SRC homology 3 domains: multifaceted binding modules
Journal ArticleTrends Biochem Sci, 47 (9), 2022.
Proximity-dependent Mapping of the Androgen Receptor Identifies Kruppel-like Factor 4 as a Functional Partner
Journal ArticleMol Cell Proteomics, 20 , 2021.
Protein context shapes the specificity of SH3 domain-mediated interactions in vivo
Journal ArticleNat Commun, 12 (1), 2021.
Tyrosine phosphorylation of DEPTOR functions as a molecular switch to activate mTOR signaling
Journal ArticleJ Biol Chem, 297 (5), 2021.
The SHCA adapter protein cooperates with lipoma-preferred partner in the regulation of adhesion dynamics and invadopodia formation
Journal ArticleJ Biol Chem, 295 (31), 2020.
Polypharmacological Perturbation of the 14-3-3 Adaptor Protein Interactome Stimulates Neurite Outgrowth
Journal ArticleCell Chem Biol, 27 (6), 2020.
Active projects
- Chaire de recherche du Canada en Protéomique du Cancer, from 2020-10-01 to 2025-09-30
- Regroupement Québécois de Recherche sur la Fonction, l’Ingénierie et les Applications des Protéines, from 2024-04-01 to 2030-03-31
- Régulation de la morphogenèse tissulaire par la signalisation dépendante des récepteurs EPH et des ligands éphrines, from 2024-04-01 to 2027-03-31
- Understanding the specificity and regulation of NCK adaptor proteins, from 2024-04-01 to 2029-03-31
Recently finished projects
- Analysis of regulatory mechanisms for receptor tyrosine kinases-initiated signaling networks assembly, from 2023-01-09 to 2023-08-25
- Analysis of SRC Homology (SH) modular domains protein interactions, from 2023-04-01 to 2024-03-31
- PROTEO, le regroupement québécois de recherche sur la fonction, l'ingénierie et les applications des protéines (PROTEO), from 2015-04-01 to 2023-03-31
- Régulation de la signalisation cellulaire par les récepteurs tyrosine kinase de la famille EPH et par leur ligands membranaires, les éphrines, from 2021-04-01 to 2024-03-31
- Regulation of oncogenic receptor tyrosine kinase signalling networks by protein phosphorylation, from 2019-04-01 to 2024-03-31
- Understanding the specificity and regulation of NCK adaptor proteins, from 2018-04-01 to 2024-03-31