Evidence map›Paper›PMID 33800852›Full record

ArticleCancers2021

Fatty Acid Synthase Confers Tamoxifen Resistance to ER+/HER2+ Breast Cancer.

Javier A Menendez, Adriana Papadimitropoulou, Travis Vander Steen, Elisabet Cuyàs, Bharvi P Oza-Gajera, Sara Verdura, Ingrid Espinoza, Luciano Vellon, Inderjit Mehmi, Ruth Lupu

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

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  16. Role of EGFR and FASN in breast cancer progression.Journal of cell communication and signaling · 2023
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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 4 countries.

Javier A MenendezMetabolism and Cancer Group, Program Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007 Girona, Spain.ORCID 0000-0001-8733-4561
Adriana PapadimitropoulouCenter of Basic Research, Biomedical Research Foundation of the Academy of Athens, 115 27 Athens, Greece.
Travis Vander SteenDepartment of Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Elisabet CuyàsMetabolism and Cancer Group, Program Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007 Girona, Spain.
Bharvi P Oza-GajeraDivision of Nephrology, University of Cincinnati, Cincinnati, OH 45267, USA.
Sara VerduraMetabolism and Cancer Group, Program Against Cancer Therapeutic Resistance (ProCURE), Catalan Institute of Oncology, 17007 Girona, Spain.ORCID 0000-0001-8980-0423
Ingrid EspinozaSchool of Population Health, University of Mississippi Medical Center, Jackson, MO 39216, USA.
Luciano VellonStem Cells Laboratory, Institute of Biology and Experimental Medicine (IBYME-CONICET), Buenos Aires C1428ADN, Argentina.
Inderjit MehmiThe Angeles Clinic & Research Institute, Cedar Sinai affiliate, Los Angeles, CA 90025, USA.
Ruth LupuDepartment of Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic, Rochester, MN 55905, USA.
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 · ARUniversity of Cincinnati · USUniversity 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-PNCI NIH HHS R01 CA116623U.S. Department of Defense BC151072U.S. Department of Defense BC151072P1
6 · The paper itself

Abstract

The identification of clinically important molecular mechanisms driving endocrine resistance is a priority in estrogen receptor-positive (ER+) breast cancer. Although both genomic and non-genomic cross-talk between the ER and growth factor receptors such as human epidermal growth factor receptor 2 (HER2) has frequently been associated with both experimental and clinical endocrine therapy resistance, combined targeting of ER and HER2 has failed to improve overall survival in endocrine non-responsive disease. Herein, we questioned the role of fatty acid synthase (FASN), a lipogenic enzyme linked to HER2-driven breast cancer aggressiveness, in the development and maintenance of hormone-independent growth and resistance to anti-estrogens in ER/HER2-positive (ER+/HER2+) breast cancer. The stimulatory effects of estradiol on

Indexed as

endocrine resistanceestrogen receptorfatty acid synthaseHER2tamoxifen

Identifiers

PMID33800852
PMCPMC7961649
OpenAlexW3135453266

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.