Evidence map›Paper›PMID 35526196›Full record

ArticleCellular and molecular life sciences : CMLS2022

Curcumin and NCLX inhibitors share anti-tumoral mechanisms in microsatellite-instability-driven colorectal cancer.

Maxime Guéguinou, Sajida Ibrahim, Jérôme Bourgeais, Alison Robert, Trayambak Pathak, Xuexin Zhang, David Crottès, Jacques Dupuy, David Ternant, Valérie Monbet and 21 more

Open access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Article
  5. Mitochondrial CaJournal of cellular physiology · 2025
    Review
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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

31 authors at 7 institutions in 3 countries.

Maxime GuéguinouEA 7501 GICC, Université de Tours, Tours, France. maxime.gueguinou@univ-tours.fr.ORCID http://orcid.org/0000-0002-5793-2082
Sajida IbrahimEA 7501 GICC, Université de Tours, Tours, France.
Jérôme BourgeaisCNRS ERL 7001 LNOx, Tours, France.
Alison RobertN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Trayambak PathakDepartment of Cellular and Molecular Physiology, College of Medicine, The Pennsylvania State University, 500 University Dr, Hershey, PA, 17033, USA.
Xuexin ZhangDepartment of Cellular and Molecular Physiology, College of Medicine, The Pennsylvania State University, 500 University Dr, Hershey, PA, 17033, USA.
David CrottèsN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Jacques DupuyTOXALIM (Research Centre in Food Toxicology)-Team E9-PPCA, Université de Toulouse, UMR 1331 INRAE, ENVT, INP-Purpan, UPS, Toulouse, France.
David TernantEA 7501 GICC, Université de Tours, Tours, France.
Valérie MonbetIRMAR Mathematics Research Institute of Rennes, UMR-CNRS 6625, Rennes, France.
Roseline GuibonN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Hector Flores-RomeroInstitute for Genetics, University of Cologne, Cologne, Germany.
Antoine LefèvreUMR 1253, iBrain, Université de Tours, Inserm, 37000, Tours, France.
Stéphanie LerondelCNRS UPS44, CIPA, PHENOMIN-TAAM, Orléans, France.
Alain Le PapeCNRS UPS44, CIPA, PHENOMIN-TAAM, Orléans, France.
Jean-François DumasN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Philippe G FrankN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Alban GiraultLaboratory of Cellular and Molecular Physiology, UR UPJV 4667, University of Picardie Jules Verne, Amiens, France.
Romain ChautardEA 7501 GICC, Université de Tours, Tours, France.
Françoise GuéraudTOXALIM (Research Centre in Food Toxicology)-Team E9-PPCA, Université de Toulouse, UMR 1331 INRAE, ENVT, INP-Purpan, UPS, Toulouse, France.
Ana J García-SáezInstitute for Genetics, University of Cologne, Cologne, Germany.
Mehdi OuaissiEA4245 Transplant Immunology and Inflammation, Université de Tours, 10 Boulevard Tonnellé, 37032, Tours, France.
Patrick EmondUMR 1253, iBrain, Université de Tours, Inserm, 37000, Tours, France.
Olivier SireIRDL Institut de Recherche Dupuy de Lôme, UMR-CNRS, 06027, Vannes, France.
Olivier HéraultCNRS ERL 7001 LNOx, Tours, France.
Gaëlle Fromont-HankardN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
Christophe VandierN2C, Nutrition Growth and Cancer, Faculté de Médecine, Université de Tours, Inserm, UMR 1069, Tours, France.
David TougeronHepato-Gastroenterology Department, Poitiers University Hospital and Faculty of Medicine of Poitiers, 86000, Poitiers, France.
Mohamed TrebakDepartment of Cellular and Molecular Physiology, College of Medicine, The Pennsylvania State University, 500 University Dr, Hershey, PA, 17033, USA.
William Raoul *EA 7501 GICC, Université de Tours, Tours, France.
Thierry Lecomte *EA 7501 GICC, Université de Tours, Tours, France. thierry.lecomte@univ-tours.fr.
Université de Tours · FRCentre National de la Recherche Scientifique · FRPennsylvania State University · USUniversité Toulouse III - Paul Sabatier · FRUniversity of Cologne · DELaboratoire de physiologie cellulaire et moléculaire · FRUniversité de Poitiers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsRecent evidences highlight a role of the mitochondria calcium homeostasis in the development of colorectal cancer (CRC). To overcome treatment resistance, we aimed to evaluate the role of the mitochondrial sodium-calcium-lithium exchanger (NCLX) and its targeting in CRC. We also identified curcumin as a new inhibitor of NCLX.

methodsWe examined whether curcumin and pharmacological compounds induced the inhibition of NCLX-mediated mitochondrial calcium (mtCa

resultsIn vitro, curcumin exerted strong anti-tumoral activity through its action on NCLX with mtCa

conclusionsOur findings highlight a novel anti-tumoral mechanism of curcumin through its action on NCLX and mitochondria calcium overload that could benefit for therapeutic schedule of patients with MSI CRC.

Indexed as

Colorectal NeoplasmsCurcuminMicrosatellite InstabilitySodium-Calcium ExchangerAnimalsCalciumCalcium SignalingHumansMiceMicrosatellite RepeatsMitochondrial ProteinsCalciumCurcuminMitochondrial ProteinsSodium-Calcium ExchangerCalcium signalingColorectal cancerCurcuminMitochondriaNCLX

Identifiers

PMID35526196
PMCPMC11072810
OpenAlexW4229332948

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.