Evidence map›Paper›PMID 39349429›Full record

ArticleCell death discovery2024

Fatty acid synthase (FASN) is a tumor-cell-intrinsic metabolic checkpoint restricting T-cell immunity.

Elisabet Cuyàs, Stefano Pedarra, Sara Verdura, Miguel Angel Pardo, Roderic Espin Garcia, Eila Serrano-Hervás, Àngela Llop-Hernández, Eduard Teixidor, Joaquim Bosch-Barrera, Eugeni López-Bonet and 6 more

Abstract read
In one paragraph

Article in Cell death discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
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  8. Article
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  12. Weight Loss-Associated Remodeling of Adipose Tissue Immunometabolism.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  13. Review
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  15. Palmitoylation modulates antitumor immunity.Molecular biology reports · 2025
    Review
  16. Review
  17. Integrating Metabolic Modulation and Nanomedicine for Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  18. Mitochondrial metabolism and cancer therapeutic innovation.Signal transduction and targeted therapy · 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

16 authors.

Elisabet Cuyàs *Program Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain.ORCID http://orcid.org/0000-0001-5353-440X
Stefano Pedarra *Centre de Recerca Matemàtica (CRM), 08193, Bellaterra, Barcelona, Spain.
Sara Verdura *Program Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain.
Miguel Angel PardoProCURE, Catalan Institute of Oncology, Oncobell, Bellvitge Institute for Biomedical Research (IDIBELL), 08908 L'Hospitalet de Llobregat, Barcelona, Spain.ORCID http://orcid.org/0000-0003-4823-6613
Roderic Espin GarciaProCURE, Catalan Institute of Oncology, Oncobell, Bellvitge Institute for Biomedical Research (IDIBELL), 08908 L'Hospitalet de Llobregat, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2494-0964
Eila Serrano-HervásProgram Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain.ORCID http://orcid.org/0000-0002-9477-0350
Àngela Llop-HernándezProgram Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain.
Eduard TeixidorMedical Oncology, Catalan Institute of Oncology, 17007, Girona, Spain.
Joaquim Bosch-BarreraMedical Oncology, Catalan Institute of Oncology, 17007, Girona, Spain.ORCID http://orcid.org/0000-0002-0893-7821
Eugeni López-BonetMetabolism and Cancer Group, Girona Biomedical Research Institute (IDIBGI), 17190, Girona, Spain.
Begoña Martin-CastilloMetabolism and Cancer Group, Girona Biomedical Research Institute (IDIBGI), 17190, Girona, Spain.
Ruth LupuDivision of Experimental Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0002-5564-3172
Miguel Angel PujanaProgram Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain.ORCID http://orcid.org/0000-0003-3222-4044
Josep SardanyèsCentre de Recerca Matemàtica (CRM), 08193, Bellaterra, Barcelona, Spain.ORCID http://orcid.org/0000-0001-7225-5158
Tomás AlarcónCentre de Recerca Matemàtica (CRM), 08193, Bellaterra, Barcelona, Spain.
Javier A MenendezProgram Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007, Girona, Spain. jmenendez@idibgi.org.ORCID http://orcid.org/0000-0001-8733-4561

Funding

Fatty Acid Synthase:Molecular Target for Breast Cancer Therapy & ChemopreventionR01CA116623 · NCI · NORTHSHORE UNIV HEALTHSYSTEM RES INST · PI LUPU, RUTH · 2005 to 2014
$3.4M
CATECHOLAMINES AND REPRODUCTIVE AGINGR01AG002021 · NIA · UNIVERSITY OF FLORIDA · PI SIMPKINS, JAMES W. · 1985 to 1990
–
Generalitat de Catalunya (Government of Catalonia) 2022 INV-1 00001Generalitat de Catalunya (Government of Catalonia) SGR 2021-00184Generalitat de Catalunya (Government of Catalonia) SLT017/20/000072Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) CM22/00276Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) CP20/00003Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI21/0136Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI22/00297NCI NIH HHS R01 CA116623U.S. Department of Defense (United States Department of Defense) BC151072U.S. Department of Defense (United States Department of Defense) BC151072P1
6 · The paper itself

Abstract

Fatty acid synthase (FASN)-catalyzed endogenous lipogenesis is a hallmark of cancer metabolism. However, whether FASN is an intrinsic mechanism of tumor cell defense against T cell immunity remains unexplored. To test this hypothesis, here we combined bioinformatic analysis of the FASN-related immune cell landscape, real-time assessment of cell-based immunotherapy efficacy in CRISPR/Cas9-based FASN gene knockout (FASN KO) cell models, and mathematical and mechanistic evaluation of FASN-driven immunoresistance. FASN expression negatively correlates with infiltrating immune cells associated with cancer suppression, cytolytic activity signatures, and HLA-I expression. Cancer cells engineered to carry a loss-of-function mutation in FASN exhibit an enhanced cytolytic response and an accelerated extinction kinetics upon interaction with cytokine-activated T cells. Depletion of FASN results in reduced carrying capacity, accompanied by the suppression of mitochondrial OXPHOS and strong downregulation of electron transport chain complexes. Targeted FASN depletion primes cancer cells for mitochondrial apoptosis as it synergizes with BCL-2/BCL-X

Identifiers

PMID39349429
PMCPMC11442875

What OpenQuestion holds

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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.