Evidence map›Paper›PMID 33081219›Full record

ArticleInternational journal of molecular sciences2020

Fatty Acid Synthase Is a Key Enabler for Endocrine Resistance in Heregulin-Overexpressing Luminal B-Like Breast Cancer.

Javier A Menendez, Inderjit Mehmi, Adriana Papadimitropoulou, Travis Vander Steen, Elisabet Cuyàs, Sara Verdura, Ingrid Espinoza, Luciano Vellon, Ella Atlas, Ruth Lupu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  13. Obesity and endocrine therapy resistance in breast cancer: Mechanistic insights and perspectives.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2022
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  18. Prognostic Significance ofDiagnostics (Basel, Switzerland) · 2021
    Article
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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

10 authors at 7 institutions in 5 countries.

Javier A MenendezProgram Against Cancer Therapeutic Resistance (ProCURE), Metabolism and Cancer Group, Catalan Institute of Oncology, 17007 Girona, Spain.ORCID 0000-0001-8733-4561
Inderjit MehmiThe Angeles Clinic and Research Institute, Cedar Sinai affiliate, Los Angeles, CA 90025, USA.
Adriana PapadimitropoulouCenter of Basic Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Travis Vander SteenMayo Clinic, Division of Experimental Pathology, Department of Laboratory Medicine and Pathology, Rochester, MN 55905, USA.
Elisabet CuyàsProgram Against Cancer Therapeutic Resistance (ProCURE), Metabolism and Cancer Group, Catalan Institute of Oncology, 17007 Girona, Spain.
Sara VerduraProgram Against Cancer Therapeutic Resistance (ProCURE), Metabolism and Cancer Group, Catalan Institute of Oncology, 17007 Girona, Spain.ORCID 0000-0001-8980-0423
Ingrid EspinozaSchool of Population Health, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Luciano VellonStem Cells Laboratory, Institute of Biology and Experimental Medicine (IBYME-CONICET), Buenos Aires C1428ADN, Argentina.
Ella AtlasEnvironmental Health Science and Research Bureau, Health Canada, Ottawa, ON K1A 0K9, Canada.
Ruth LupuCenter of Basic Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Institut Català d'Oncologia · ESMayo Clinic · USAngeles Clinic and Research Institute · USBiomedical Research Foundation of the Academy of Athens · GRConsejo Nacional de Investigaciones Científicas y Técnicas · ARHealth Canada · CAUniversity of Mississippi Medical Center · US

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
Ministerio de Ciencia e Innovación PID2019-10455GB-I00Ministerio de Ciencia e Innovación SAF2016-80639-PNIH HHS R01 CA116623U.S. Department of Defense BC151072U.S. Department of Defense BC151072P1
6 · The paper itself

Abstract

HER2 transactivation by the HER3 ligand heregulin (HRG) promotes an endocrine-resistant phenotype in the estrogen receptor-positive (ER+) luminal-B subtype of breast cancer. The underlying biological mechanisms that link them are, however, incompletely understood. Here, we evaluated the putative role of the lipogenic enzyme fatty acid synthase (FASN) as a major cause of HRG-driven endocrine resistance in ER+/HER2-negative breast cancer cells. MCF-7 cells engineered to stably overexpress HRG (MCF-7/HRG), an in vitro model of tamoxifen/fulvestrant-resistant luminal B-like breast cancer, showed a pronounced up-regulation of

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic Agents, HormonalBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFatty Acid Synthase, Type IFemaleFulvestrantHistidine-Rich GlycoproteinHumansMAP Kinase Signaling SystemMCF-7 CellsMiceMice, NudePhosphatidylinositol 3-KinasesProteinsAntineoplastic Agents, HormonalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFASN protein, humanFatty Acid Synthase, Type IFulvestrantHistidine-Rich GlycoproteinPhosphatidylinositol 3-KinasesProteinsProto-Oncogene Proteins c-aktTamoxifenendocrine resistancefulvestrantluminaltamoxifen

Identifiers

PMID33081219
PMCPMC7588883
OpenAlexW3092926590

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.