Evidence map›Paper›PMID 32295603›Full record

ArticleBreast cancer research : BCR2020

Cetuximab PET delineated changes in cellular distribution of EGFR upon dasatinib treatment in triple negative breast cancer.

Brooke N McKnight, Seongho Kim, Julie L Boerner, Nerissa T Viola

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  6. Review
  7. Advances in PET/CT Imaging for Breast Cancer.Journal of clinical medicine · 2023
    Review
  8. 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

4 authors at 2 institutions in 1 country.

Brooke N McKnightDepartment of Oncology, Karmanos Cancer Institute Wayne State University, 4100 John R Street, Detroit, MI, 48201, USA.
Seongho KimDepartment of Oncology, Biostatistics Core, Karmanos Cancer Institute Wayne State University, Detroit, MI, 48201, USA.
Julie L BoernerDepartment of Oncology, Karmanos Cancer Institute Wayne State University, 4100 John R Street, Detroit, MI, 48201, USA.
Nerissa T ViolaDepartment of Oncology, Karmanos Cancer Institute Wayne State University, 4100 John R Street, Detroit, MI, 48201, USA. violan@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Delineating tumors with resistance to tyrosine kinase therapy via PET imagingR00CA181492 · NCI · WAYNE STATE UNIVERSITY · PI VIOLA, NERISSA THERESE · 2015 to 2017
$662k
National Cancer Institute (US) T32 CAA09531NCI NIH HHS P30 CA022453NCI NIH HHS R00 CA181492
6 · The paper itself

Abstract

backgroundAt least 50% of triple negative breast cancer (TNBC) overexpress the epidermal growth factor receptor, EGFR, which paved the way for clinical trials investigating its blockade. Outcomes remained dismal stemming from mechanisms of resistance particularly the nuclear cycling of EGFR, which is enhanced by Src activation. Attenuation of Src reversed nuclear translocation, restoring EGFR to the cell surface. Herein, we hypothesize that changes in cellular distribution of EGFR upon Src inhibition with dasatinib can be annotated through the EGFR immunopositron emission tomography (immunoPET) radiotracer, [

methodsNuclear and non-nuclear EGFR levels of dasatinib-treated vs. untreated MDA-MB-231 and MDA-MB-468 cells were analyzed via immunoblots. Both treated and untreated cells were exposed to [

resultsTreated cells displayed higher binding of [

conclusionsCetuximab PET can monitor effects of dasatinib on EGFR cellular distribution and potentially inform treatment response in wild-type KRAS TNBC.

Indexed as

Cell ProliferationAnimalsAntineoplastic Agents, ImmunologicalCell Line, TumorCetuximabDasatinibDrug Resistance, NeoplasmErbB ReceptorsFemaleHumansMiceMice, NudePositron-Emission TomographyProtein Kinase InhibitorsRadioisotopesTriple Negative Breast NeoplasmsAntineoplastic Agents, ImmunologicalCetuximabDasatinibEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsRadioisotopesZirconiumZirconium-89DasatinibEGFR PET imagingNuclear EGFR translocationSrcTriple negative breast cancer

Identifiers

PMID32295603
PMCPMC7160960
OpenAlexW3016919412

What OpenQuestion holds

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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.