Evidence map›Paper›PMID 39956817›Full record

ArticleNature communications2025

Targeting ELOVL6 to disrupt c-MYC driven lipid metabolism in pancreatic cancer enhances chemosensitivity.

Ana García García, María Ferrer Aporta, Germán Vallejo Palma, Antonio Giráldez Trujillo, Raquel Castillo-González, David Calzón Lozano, Alberto Mora Perdiguero, Raúl Muñoz Velasco, Miguel Colina Castro, Elena de Simone Benito and 14 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  14. Fueling the fire-a pan-cancer analysis of MYC-regulated lipid metabolism.Frontiers in cell and developmental biology · 2025
    Review
  15. Review
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

24 authors.

Ana García GarcíaGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0000-0001-7875-4943
María Ferrer AportaGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0000-0003-4349-1797
Germán Vallejo PalmaGrupo de Oncología Cutánea. Servicio de Anatomía Patológica, Hospital Universitario 12 de Octubre. Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avenida de Cordoba s/n, 28041, Madrid, Spain.ORCID http://orcid.org/0009-0001-0770-0355
Antonio Giráldez TrujilloGrupo de Oncología Cutánea. Servicio de Anatomía Patológica, Hospital Universitario 12 de Octubre. Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avenida de Cordoba s/n, 28041, Madrid, Spain.
Raquel Castillo-GonzálezGrupo de Oncología Cutánea. Servicio de Anatomía Patológica, Hospital Universitario 12 de Octubre. Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avenida de Cordoba s/n, 28041, Madrid, Spain.
David Calzón LozanoGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0009-0003-3480-9908
Alberto Mora PerdigueroGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0000-0001-6306-5467
Raúl Muñoz VelascoGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0000-0003-0621-167X
Miguel Colina CastroGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.
Elena de Simone BenitoGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.
Raúl Torres-RuizMolecular Cytogenetics and Genome Editing Unit, Human Cancer Genetics Program, Centro Nacional de Investigaciones Oncológicas (CNIO), 28029, Madrid, Spain.ORCID http://orcid.org/0000-0001-9606-0398
Sandra Rodriguez-PeralesMolecular Cytogenetics and Genome Editing Unit, Human Cancer Genetics Program, Centro Nacional de Investigaciones Oncológicas (CNIO), 28029, Madrid, Spain.ORCID http://orcid.org/0000-0001-7221-3636
Jonas DehairsLaboratory of Lipid Metabolism and Cancer, Department of Oncology, KU Leuven, 3000, Leuven, Belgium.ORCID http://orcid.org/0000-0002-6789-2264
Johannes V SwinnenLaboratory of Lipid Metabolism and Cancer, Department of Oncology, KU Leuven, 3000, Leuven, Belgium.ORCID http://orcid.org/0000-0002-7720-5077
Juan Carlos Garcia-CañaverasBiomarkers and Precision Medicine Unit, Health Research Institute La Fe, Av. Fernando Abril Martorell, 106, 46026, Valencia, Spain.ORCID http://orcid.org/0000-0001-7112-1537
Agustín LahozBiomarkers and Precision Medicine Unit, Health Research Institute La Fe, Av. Fernando Abril Martorell, 106, 46026, Valencia, Spain.ORCID http://orcid.org/0000-0001-7232-0626
Sandra Montalvo QuirósBiofísica Computacional y Análisis de Datos Biológicos, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.
Carlos Del Pozo-RojasBiofísica Computacional y Análisis de Datos Biológicos, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.ORCID http://orcid.org/0009-0003-8128-4438
Clara Luque RiojaDepartment of Physical Chemistry, Complutense University of Madrid, 28040, Madrid, Spain.
Francisco MonroyDepartment of Physical Chemistry, Complutense University of Madrid, 28040, Madrid, Spain.ORCID http://orcid.org/0000-0001-6455-3083
Diego Herráez-AguilarBiofísica Computacional y Análisis de Datos Biológicos, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain.
Marina Alonso RiañoGrupo de Oncología Cutánea. Servicio de Anatomía Patológica, Hospital Universitario 12 de Octubre. Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avenida de Cordoba s/n, 28041, Madrid, Spain.ORCID http://orcid.org/0000-0003-1293-1075
José Luis Rodríguez PeraltoGrupo de Oncología Cutánea. Servicio de Anatomía Patológica, Hospital Universitario 12 de Octubre. Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Avenida de Cordoba s/n, 28041, Madrid, Spain.
Víctor Javier Sánchez-Arévalo LoboGrupo de Oncología Molecular, Instituto de Investigaciones Biosanitarias, Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcón, 28223, Madrid, Spain. victor.sanchezarevalo@ufv.es.ORCID http://orcid.org/0000-0002-4561-1505

Funding

Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI22/00492Universidad Francisco de Vitoria (Francisco de Vitoria University) UFV2022-23
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer with a 12% survival rate, highlighting the need for novel therapies. c-MYC overexpression, driven by upstream mutations and amplifications, reprograms tumor metabolism and promotes proliferation, migration and metastasis. This study identifies ELOVL6, a fatty acid elongase regulated by c-MYC, as a potential therapeutic target. Using PDAC mouse models and cell lines, we show that c-MYC directly upregulates ELOVL6 during tumor progression. Genetic or chemical inhibition of ELOVL6 reduces proliferation and migration by altering fatty acid composition, affecting membrane rigidity, permeability and pinocytosis. These changes increase Abraxane uptake and show a synergistic effect when combined with ELOVL6 inhibition in vitro. In vivo, ELOVL6 interference significantly suppresses tumor growth and improves Abraxane response, prolonging survival. These findings position ELOVL6 as a promising target for improving PDAC treatment outcomes.

Indexed as

AcetyltransferasesCarcinoma, Pancreatic DuctalLipid MetabolismPancreatic NeoplasmsProto-Oncogene Proteins c-mycAnimalsCell Line, TumorCell MovementCell ProliferationFatty Acid ElongasesFemaleGene Expression Regulation, NeoplasticHumansMiceXenograft Model Antitumor AssaysAcetyltransferasesELOVL6 protein, humanElovl6 protein, mouseFatty Acid ElongasesMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID39956817
PMCPMC11830767

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.