Evidence map›Paper›PMID 41120088›Full record

ArticleMolecular metabolism2025

Canagliflozin synergises with serine restriction mediating anti-leukaemic effects in T-cell acute lymphoblastic leukaemia.

Fernando M Ponce-Garcia, Yasmin R Jenkins, Victoria D Assmann, Silpita Paul, Nitesh D Sharma, Catherine Moore, Eric H Ma, Paraskevi Diamanti, Marc Hennequart, Julianna Blagih and 12 more

Abstract read
In one paragraph

Article in Molecular metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Fernando M Ponce-GarciaInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
Yasmin R JenkinsInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
Victoria D AssmannWolfson Wohl Cancer Research Centre, School of Cancer Sciences, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Silpita PaulDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Nitesh D SharmaDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Catherine MooreInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
Eric H MaDepartment of Metabolism and Nutritional Programming, Van Andel Institute, Grand Rapids, MI, USA.
Paraskevi DiamantiCellular and Molecular Medicine, University of Bristol, Biomedical Sciences Building, Bristol, BS8 1TD, United Kingdom; NHS Blood and Transplant, Filton, Bristol, BS34 7QH, United Kingdom.
Marc HennequartThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, United Kingdom; Namur Research Institute for Life Sciences (NARILIS), Molecular Physiology Unit (URPHYM), University of Namur, Namur, Belgium.
Julianna BlagihThe Francis Crick Institute, 1 Midland Road, London, NW1 1AT, United Kingdom; University of Montreal, Maisonneuve-Rosemont Hospital Research Centre, 5414 Assomption Blvd, Montreal, H1T 2M4, Canada.
Le LeRutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, NJ, USA.
Benjamin J JenkinsInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
Sophie RouvrayInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
James G CroninInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom.
Russell G JonesDepartment of Metabolism and Nutritional Programming, Van Andel Institute, Grand Rapids, MI, USA.
Marc MansourDepartment of Haematology, Cancer Institute, University College London, London, United Kingdom.
Allison BlairCellular and Molecular Medicine, University of Bristol, Biomedical Sciences Building, Bristol, BS8 1TD, United Kingdom; NHS Blood and Transplant, Filton, Bristol, BS34 7QH, United Kingdom.
Christina HalseyWolfson Wohl Cancer Research Centre, School of Cancer Sciences, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Ksenia Matlawska-WasowskaDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Daniel HerranzRutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, NJ, USA; Department of Pharmacology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA; Department of Pediatrics, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA.
Emma E VincentSchool of Translational Health Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, BS1 3NY, United Kingdom; Integrative Epidemiology Unit, School of Population Health Science, University of Bristol, Bristol, BS8 2BN, United Kingdom. Electronic address: emma.vincent@bristol.ac.uk.
Nicholas JonesInstitute of Life Science, Swansea University Medical School, Swansea University, SA2 8PP, United Kingdom. Electronic address: n.jones@swansea.ac.uk.

Funding

The roles of SOCS5 in T-ALL migration and tissue infiltrationR01CA237165 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI MATLAWSKA-WASOWSKA, KSENIA · 2019 to 2023
$1.7M
Role of CXCR3-CXCL10 signaling in T-ALL CNS diseaseR01CA282701 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Ksenia Matlawska-Wasowska · 2024 to 2026
$1.3M
NCI NIH HHS R01 CA237165NCI NIH HHS R01 CA282701
6 · The paper itself

Abstract

T-cell acute lymphoblastic leukaemia (T-ALL) is a haematological malignancy commonly driven by NOTCH1 activating mutations. A concomitant feature associated with NOTCH1 mutations is heightened oxidative metabolism enabling the exponential proliferation of T-ALL blasts. As such, targeting mitochondrial metabolism in T-ALL is an attractive therapeutic avenue. Related to this, canagliflozin (cana), is an FDA-approved sodium glucose co-transporter 2 inhibitor with known off-target effects on complex I and glutamate dehydrogenase, but its potential anti-leukaemic effects remain unexplored. Here, we show that cana possesses potent anti-leukaemic effects underpinned by proliferative defects, cell cycle disruption and apoptosis. These anti-leukaemic effects driven by cana, are attributed to a perturbed tricarboxylic acid (TCA) cycle and mitochondrial metabolism, and elevated mitochondrial ROS. Proteomic analysis revealed that cana treatment resulted in a compensatory increase in the expression of ATF4 targets, including upregulation of serine biosynthesis pathway and one-carbon metabolism enzymes. As such, restriction of serine and glycine synergized with cana treatment, further enhancing its anti-leukaemic effects. Collectively, our study reveals a cana-driven metabolic vulnerability that can be further exploited via dietary manipulation to treat T-ALL.

Indexed as

CanagliflozinPrecursor T-Cell Lymphoblastic Leukemia-LymphomaSerineActivating Transcription Factor 4ApoptosisCell Line, TumorCell ProliferationCitric Acid CycleHumansMitochondriaReactive Oxygen SpeciesSodium-Glucose Transporter 2 InhibitorsActivating Transcription Factor 4CanagliflozinReactive Oxygen SpeciesSerineSodium-Glucose Transporter 2 InhibitorsCanagliflozinGlycineLeukaemiaMetabolismSerineT-ALL

Identifiers

PMID41120088
PMCPMC12615362

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.