Evidence map›Paper›PMID 37253733›Full record

ArticleNature communications2023

Identification of fatty acid amide hydrolase as a metastasis suppressor in breast cancer.

Isabel Tundidor, Marta Seijo-Vila, Sandra Blasco-Benito, María Rubert-Hernández, Sandra Adámez, Clara Andradas, Sara Manzano, Isabel Álvarez-López, Cristina Sarasqueta, María Villa-Morales and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

25 authors at 10 institutions in 3 countries.

Isabel TundidorDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.
Marta Seijo-VilaDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.
Sandra Blasco-BenitoDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.
María Rubert-HernándezDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.
Sandra AdámezDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.ORCID 0000-0002-2593-5326
Clara AndradasBrain Tumor Research Program, Telethon Kids Institute, Nedlands, WA, Australia.
Sara ManzanoBreast Cancer Group, Oncology Area, Biodonostia Health Research Institute, San Sebastián, Spain.ORCID 0000-0002-0052-511X
Isabel Álvarez-LópezBreast Cancer Group, Oncology Area, Biodonostia Health Research Institute, San Sebastián, Spain.
Cristina SarasquetaUnit of Information and Healthcare Results, OSI Donostialdea, Biodonostia Health Research Institute, San Sebastián, Spain.
María Villa-MoralesCentro de Biología Molecular Severo Ochoa (CBMSO) (CSIC-UAM), Madrid, Spain.ORCID 0000-0001-7906-0169
Carmen González-LoisDepartment of Pathology, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain.ORCID 0000-0003-0169-5863
Esther Ramírez-MedinaDepartment of Obstetrics & Gynecology, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain.
Belén AlmogueraDepartment of Obstetrics & Gynecology, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain.ORCID 0000-0002-4735-0644
Antonio J Sánchez-LópezBiobank Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Laura BindilaClinical Lipidomics Unit, Institute of Physiological Chemistry, University Medical Center, Mainz, Germany.ORCID 0000-0001-5538-2008
Sigrid HamannDepartment of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Kiel, Germany.
Norbert ArnoldDepartment of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0003-4523-8808
Christoph RöckenInstitute of Pathology, University Hospital Schleswig-Holstein, Kiel, Germany.ORCID 0000-0002-6989-8002
Ignacio Heras-MurilloImmunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
David SanchoImmunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.ORCID 0000-0003-2890-3984
Gema Moreno-BuenoMD Anderson International Foundation; Instituto de Investigaciones Biomédicas Alberto Sols (CSIC-UAM); Department of Biochemistry, Autonomous University of Madrid; Instituto de Investigación Hospital Universitario La Paz (IdiPaz); Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain.ORCID 0000-0002-5030-6687
María M CaffarelBreast Cancer Group, Oncology Area, Biodonostia Health Research Institute, San Sebastián, Spain.ORCID 0000-0002-7442-6827
Manuel GuzmánDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain.ORCID 0000-0001-7475-118X
Cristina SánchezDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain. macsanch@ucm.es.ORCID 0000-0002-1428-3078
Eduardo Pérez-GómezDepartment of Biochemistry and Molecular Biology, Complutense University, Madrid, Spain. eduperez@ucm.es.ORCID 0000-0003-0160-5565
Universidad Complutense de Madrid · ESHospital Universitario Puerta de Hierro Majadahonda · ESBiogipuzkoa Health Research Institute · ESUniversity Hospital Schleswig-Holstein · DESpanish National Centre for Cardiovascular Research · ESCentro de Biología Molecular Severo Ochoa · ESHospital Universitario La Paz · ESIkerbasque · ESJohannes Gutenberg University Mainz · DEThe Kids Research Institute Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical management of breast cancer (BC) metastasis remains an unmet need as it accounts for 90% of BC-associated mortality. Although the luminal subtype, which represents >70% of BC cases, is generally associated with a favorable outcome, it is susceptible to metastatic relapse as late as 15 years after treatment discontinuation. Seeking therapeutic approaches as well as screening tools to properly identify those patients with a higher risk of recurrence is therefore essential. Here, we report that the lipid-degrading enzyme fatty acid amide hydrolase (FAAH) is a predictor of long-term survival in patients with luminal BC, and that it blocks tumor progression and lung metastasis in cell and mouse models of BC. Together, our findings highlight the potential of FAAH as a biomarker with prognostic value in luminal BC and as a therapeutic target in metastatic disease.

Indexed as

AmidohydrolasesBiomarkers, TumorLung NeoplasmsAnimalsFatty Acid Amide HydrolasesMiceNeoplasm Recurrence, LocalAmidohydrolasesBiomarkers, TumorFatty Acid Amide Hydrolases

Identifiers

PMID37253733
PMCPMC10229544
OpenAlexW4378783290

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.