Evidence map›Paper›PMID 31676791›Full record

ArticleNature communications2019

Essentiality of fatty acid synthase in the 2D to anchorage-independent growth transition in transforming cells.

Maria J Bueno, Veronica Jimenez-Renard, Sara Samino, Jordi Capellades, Alejandra Junza, María Luz López-Rodríguez, Javier Garcia-Carceles, Irene Lopez-Fabuel, Juan P Bolaños, Navdeep S Chandel and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. The metabolic profiles of cancer stem cells.Stem cell research & therapy · 2026
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  18. Metabolomics in oncology.Cancer reports (Hoboken, N.J.) · 2023
    Review
  19. Article
  20. Article
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

13 authors at 6 institutions in 2 countries.

Maria J BuenoBreast Cancer Clinical Research Unit, CNIO - Spanish National Cancer Research Center, Madrid, Spain.
Veronica Jimenez-RenardBreast Cancer Clinical Research Unit, CNIO - Spanish National Cancer Research Center, Madrid, Spain.
Sara SaminoMetabolomics Platform, Department of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, Spain.
Jordi CapelladesMetabolomics Platform, Department of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, Spain.
Alejandra JunzaMetabolomics Platform, Department of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, Spain.
María Luz López-RodríguezQuimica Organica I, Universidad Complutense, Madrid, Spain.
Javier Garcia-CarcelesQuimica Organica I, Universidad Complutense, Madrid, Spain.ORCID http://orcid.org/0000-0003-4614-9639
Irene Lopez-FabuelInstitute of Functional Biology and Genomics (IBFG), Universidad de Salamanca, CSIC, Salamanca, Spain.ORCID http://orcid.org/0000-0002-3049-748X
Juan P BolañosInstitute of Functional Biology and Genomics (IBFG), Universidad de Salamanca, CSIC, Salamanca, Spain.ORCID http://orcid.org/0000-0002-3949-6862
Navdeep S ChandelDepartment of Medicine, Northwestern University Feinberg School of Medicine Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-7208-3886
Oscar YanesMetabolomics Platform, Department of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, Spain.ORCID http://orcid.org/0000-0003-3695-7157
Ramon ColomerMedical Oncology Hospital, Universitario La Princesa, Madrid, Spain.ORCID http://orcid.org/0000-0002-6393-3444
Miguel Quintela-FandinoBreast Cancer Clinical Research Unit, CNIO - Spanish National Cancer Research Center, Madrid, Spain. mquintela@cnio.es.
Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESSpanish National Cancer Research Centre · ESUniversidad Complutense de Madrid · ESUniversidad de Salamanca · ESHospital Universitario de La Princesa · ESNorthwestern University · US

Funding

Mitochondrial metabolism and ROS regulate cancerR35CA197532 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CHANDEL, NAVDEEP S · 2016 to 2022
$6.3M
NCI NIH HHS R35 CA197532
6 · The paper itself

Abstract

Upregulation of fatty acid synthase (FASN) is a common event in cancer, although its mechanistic and potential therapeutic roles are not completely understood. In this study, we establish a key role of FASN during transformation. FASN is required for eliciting the anaplerotic shift of the Krebs cycle observed in cancer cells. However, its main role is to consume acetyl-CoA, which unlocks isocitrate dehydrogenase (IDH)-dependent reductive carboxylation, producing the reductive power necessary to quench reactive oxygen species (ROS) originated during the switch from two-dimensional (2D) to three-dimensional (3D) growth (a necessary hallmark of cancer). Upregulation of FASN elicits the 2D-to-3D switch; however, FASN's synthetic product palmitate is dispensable for this process since cells satisfy their fatty acid requirements from the media. In vivo, genetic deletion or pharmacologic inhibition of FASN before oncogenic activation prevents tumor development and invasive growth. These results render FASN as a potential target for cancer prevention studies.

Indexed as

AnimalsCell LineCells, CulturedEmbryo, MammalianEmbryonic Stem CellsFatty AcidsFatty Acid SynthasesFemaleFibroblastsHEK293 CellsHumansMaleMice, Inbred C57BLMice, KnockoutMice, NudeMice, TransgenicFatty AcidsFatty Acid Synthases

Identifiers

PMID31676791
PMCPMC6825217
OpenAlexW2988078029

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.