Laura Hulea
mRNA translation, cellular metabolism and adaptation in cancer
- Professeure sous octroi agrégé
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Faculté de médecine - Département de médecine
- Professeure accréditée
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Faculté de médecine - Département de biochimie et médecine moléculaire
- Professeure accréditée
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Faculté de médecine - Département de pharmacologie et physiologie
Profile
Research expertise
The Hulea Lab investigates how mRNA translation and cellular metabolism work together to shape cell function, cell state and adaptation. Its research focuses on cancer biology, with complementary projects exploring these processes in non-cancer contexts.
The team studies how signalling pathways regulate protein synthesis, including through the mTORC1–4E-BP–eIF4F axis, and how changes in gene expression and nutrient use support metabolic plasticity and stress responses. It also investigates the vulnerabilities that emerge from these adaptive programmes and how targeting them could improve responses to cancer treatment.
Cancer research in the lab spans melanoma, ovarian cancer and acute myeloid leukemia, including paediatric acute megakaryoblastic leukemia. Complementary projects investigate links between translation, metabolism and cell state in immune and adipose biology.
The laboratory combines polysome profiling, transcriptomics, proteomics, metabolomics, stable-isotope tracing and measurements of cellular bioenergetics with molecular and cellular biology and experimental cancer models.
Biography
Laura Hulea is an Associate Professor in the Department of Medicine and Medical Specialties at Université de Montréal and a principal investigator at the Centre de recherche de l’Hôpital Maisonneuve-Rosemont (CR-HMR). Her laboratory investigates how mRNA translation and cellular metabolism work together to shape cell function and adaptation, with a focus on cancer biology. She joined Université de Montréal in 2019 and established her laboratory at CR-HMR in March of that year. She was appointed Assistant Professor in 2020 and promoted to Associate Professor in 2024.
Her training spans biochemical engineering at INSA Lyon and structural and functional biochemistry at Université Claude Bernard Lyon 1. She earned her PhD in Biochemistry at McGill University in 2013, followed by postdoctoral research with Ivan Topisirovic and Michael Pollak at the Lady Davis Institute, McGill University, from 2013 to March 2019.
Laura established the metabolomics platform at CR-HMR and led it from 2021 to 2025. She chairs the centre’s Scientific Activities Committee and received its Recognition Award in 2026 for her contribution to its scientific activities and development. She holds an FRQS Junior 2 Research Scholar Award (2024–2028), following a Junior 1 award (2020–2024).
Affiliations and responsabilities
Research affiliations
Research units
Membre
Affiliated institutions
- CIUSSS de l'Est-de-l'Île-de-Montréal – Hôpital Maisonneuve-Rosemont (HMR)
Teaching and supervision
Student supervision
Theses and dissertation supervision (Papyrus Institutional Repository)
Ciblage de la machinerie traductionnelle pour surmonter la résistance aux inhibiteurs de kinase dans le mélanome
Cycle : Master's
Grade : M. Sc.
Projects
Research projects
Mélanome : traduction des ARNm et plasticité métabolique
Description
We investigate how mRNA translation and cellular metabolism contribute to melanoma adaptation to targeted therapies. We aim to understand the programmes that sustain resistant-cell survival and how targeting the translation machinery, particularly eIF4A, can disrupt them. Our work explores links between translation, metabolic plasticity and cell state to identify new vulnerabilities and therapeutic combination strategies.
Leucémie myéloïde aiguë : programmes de survie et vulnérabilités traductionnelles
Description
We study the links between mRNA translation, metabolism and acute myeloid leukemia cell survival, including resistance to venetoclax and azacitidine. We investigate how eIF4A inhibition disrupts adaptive programmes and metabolic plasticity in leukemic cells, and how these vulnerabilities can be exploited through therapeutic combinations.
Project jointly led by Laura Hulea and François Mercier, Lady Davis Institute, McGill University.
Leucémie aiguë mégacaryoblastique pédiatrique : vulnérabilités métaboliques
Description
In pediatric acute megakaryoblastic leukemia associated with the CBFA2T3::GLIS2 fusion, our contribution focuses on cellular metabolic rewiring. We investigate how this fusion alters nutrient use and bioenergetics, and identify metabolic dependencies that sustain leukemic-cell growth and survival. Our goal is to evaluate the potential of targeting these dependencies, alone or in combination with other therapeutic approaches.
In collaboration with Frédérick A. Mallette, CR-HMR.
Cancer de l’ovaire : traduction des ARNm et résistance au platine
Description
We investigate how selective mRNA translation contributes to epithelial ovarian cancer growth and resistance to platinum-based chemotherapy. We study eIF4A-dependent programmes that support cell survival and DNA-damage responses. Our goal is to identify translational vulnerabilities and evaluate combination strategies that could improve treatment responses in preclinical models.
In collaboration with Hugo Wurtele, CR-HMR.
Outreach
Publications and presentations
Publications
Prépublication · 2026
eIF4A inhibition disrupts resistance-associated translational and metabolic programs in BRAF-mutant melanoma
Schcolnik-Cabrera, Takdenti, Sadr Hashemi Nejad et al. bioRxiv (2026).
Publications sélectionnées
Une sélection de travaux du laboratoire, de projets collaboratifs et de recherches antérieures de Laura Hulea.
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Translational control of leukemic metabolism and disease progression
Mercier et al. Trends in Cell Biology (2025), 35(11):971–986. -
Protocol to perform polysome profiling in primary differentiating murine adipocytes
De Siqueira, Nouhi et al. STAR Protocols (2025), 6(2):103799. -
Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Gife et al. Journal of Visualized Experiments (JoVE) (2025), (220):e68244. -
CBFA2T3-GLIS2-dependent pediatric acute megakaryoblastic leukemia is driven by GLIS2 and sensitive to navitoclax
Neault et al. Cell Reports (2023), 42(9):113084. -
EIF4A inhibition targets bioenergetic homeostasis in AML MOLM-14 cells in vitro and in vivo and synergizes with cytarabine and venetoclax
Fooks et al. Journal of Experimental & Clinical Cancer Research (2022), 41:340. -
Translational and HIF-1α-Dependent Metabolic Reprogramming Underpin Metabolic Plasticity and Responses to Kinase Inhibitors and Biguanides
Hulea, Gravel, Morita et al. Cell Metabolism (2018), 28(6):817–832.e8.
Disciplines
- Biochemistry
- Molecular Biology
Areas of expertise
- Gene Regulation and Expression
- Metabolism
- Stress
- Cell Therapy of Cancer