Evidence map›Paper›PMID 31375515›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

A Fatty Acid Oxidation-dependent Metabolic Shift Regulates the Adaptation of

Andrea Aloia, Daniela Müllhaupt, Christophe D Chabbert, Tanja Eberhart, Stefanie Flückiger-Mangual, Ana Vukolic, Ossia Eichhoff, Anja Irmisch, Leila T Alexander, Ernesto Scibona and 16 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

93 citing papers in PubMed, 129 citations in OpenAlex.

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  19. Mitochondrial bioenergetics and networks in melanoma: an update.Apoptosis : an international journal on programmed cell death · 2025
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33 more citing papers are in PubMed but not listed here.

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

26 authors at 6 institutions in 2 countries.

Andrea AloiaInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland. werner.kovacs@biol.ethz.ch aloia.andrea@libero.it.
Daniela MüllhauptInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.ORCID 0000-0003-4167-1591
Christophe D ChabbertInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-7851-4640
Tanja EberhartInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-3621-5594
Stefanie Flückiger-MangualInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.
Ana VukolicInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.
Ossia EichhoffDepartment of Dermatology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-3319-1312
Anja IrmischDepartment of Dermatology, University Hospital Zurich, Zurich, Switzerland.
Leila T AlexanderInstitute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Ernesto ScibonaInstitute of Chemical and Bioengineering, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-2012-5674
Dennie T FrederickMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Benchun MiaoMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Tian TianDepartment of Computer Science, New Jersey Institute of Technology, Newark, New Jersey.
Chaoran ChengDepartment of Computer Science, New Jersey Institute of Technology, Newark, New Jersey.
Lawrence N KwongDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zhi WeiDepartment of Computer Science, New Jersey Institute of Technology, Newark, New Jersey.ORCID 0000-0001-6059-4267
Ryan J SullivanMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Genevieve M BolandDepartment of Surgery, Massachusetts General Hospital Cancer Center, Boston, Massachusetts.ORCID 0000-0002-7522-6173
Meenhard HerlynMolecular and Cellular Oncogenesis Program and Melanoma Research Center, The Wistar Institute, Philadelphia, Pennsylvania.
Keith T FlahertyMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Nicola ZamboniInstitute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Reinhard DummerDepartment of Dermatology, University Hospital Zurich, Zurich, Switzerland.
Gao ZhangMolecular and Cellular Oncogenesis Program and Melanoma Research Center, The Wistar Institute, Philadelphia, Pennsylvania.
Mitchell P Levesque *Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.
Wilhelm KrekInstitute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland.
Werner J Kovacs *Institute of Molecular Health Sciences, ETH Zurich, Zurich, Switzerland. werner.kovacs@biol.ethz.ch aloia.andrea@libero.it.ORCID 0000-0002-4440-4344
ETH Zurich · CHMassachusetts General Hospital · USUniversity Hospital of Zurich · CHNew Jersey Institute of Technology · USThe Wistar Institute · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2008 to 2023
$37.1M
Research Project 2 - Targeting Melanoma Tumor Survival and Apoptotic MachineryU54CA224070 · NCI · WISTAR INSTITUTE · PI Michael Davies, Meenhard F Herlyn · 2017 to 2026
$13.9M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA174523NCI NIH HHS U54 CA224070
6 · The paper itself

Abstract

purposeTreatment of EXPERIMENTAL

designBy screening proteins expressed on the cell surface of melanoma cells, we identified the fatty acid transporter CD36 as the most consistently upregulated protein upon short-term treatment with MAPKi. We further investigated the effects of MAPKi on fatty acid metabolism using

resultsMelanoma cells treated with MAPKi displayed increased levels of CD36 and of PPARα-mediated and carnitine palmitoyltransferase 1A (CPT1A)-dependent fatty acid oxidation (FAO). While CD36 is a useful marker of melanoma cells during adaptation and drug-tolerant phases, the upregulation of CD36 is not functionally involved in FAO changes that characterize MAPKi-treated cells. Increased FAO is required for

conclusionsThus, we identified a clinically relevant therapeutic approach that has the potential to improve initial responses and to delay acquired drug resistance of

Indexed as

Adaptation, BiologicalMutationOxidation-ReductionAllelesAnimalsBiomarkersCD36 AntigensCell Line, TumorCell ProliferationDisease Models, AnimalDrug Resistance, NeoplasmFatty AcidsGene Expression Regulation, NeoplasticGenotypeGlycolysisHumansBiomarkersBRAF protein, humanCD36 AntigensFatty AcidsPPAR alphaPPARA protein, humanProtein Kinase InhibitorsProto-Oncogene Proteins B-raf

Identifiers

PMID31375515
PMCPMC6906212
OpenAlexW2964974081

What OpenQuestion holds

Textmetadata
LicenceTDM
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.