Evidence map›Paper›PMID 32576280›Full record

ArticleBreast cancer research : BCR2020

New generation breast cancer cell lines developed from patient-derived xenografts.

Jessica Finlay-Schultz, Britta M Jacobsen, Duncan Riley, Kiran V Paul, Scott Turner, Andrea Ferreira-Gonzalez, J Chuck Harrell, Peter Kabos, Carol A Sartorius

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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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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

9 authors at 2 institutions in 1 country.

Jessica Finlay-SchultzDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Britta M JacobsenDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Duncan RileyDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Kiran V PaulDepartment of Medicine, Division of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Scott TurnerDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Andrea Ferreira-GonzalezDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, 23298, USA.
J Chuck HarrellDepartment of Pathology, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Peter KabosDepartment of Medicine, Division of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA. Peter.Kabos@cuanschutz.edu.
Carol A SartoriusDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA. Carol.Sartorius@cuanschutz.edu.ORCID 0000-0002-9170-3988
University of Colorado Anschutz Medical Campus · USVirginia Commonwealth University · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Progesterone Receptor (PR) Signaling Cross Talk Drives ER+ Breast CancerR01CA229697 · NCI · UNIVERSITY OF MINNESOTA · PI Carol A Lange, Douglas Yee · 2020 to 2026
$3.6M
Hormones and Tumor Initiating Cells in Human Breast CancersR01CA140985 · NCI · UNIVERSITY OF COLORADO DENVER · PI SARTORIUS, CAROL ANN · 2011 to 2020
$3.0M
Cancer-associated fibroblasts in estrogen receptor positive breast cancer.R01CA205044 · NCI · UNIVERSITY OF COLORADO DENVER · PI KABOS, PETER · 2016 to 2020
$1.8M
NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA140985NCI NIH HHS R01 CA205044NCI NIH HHS R01 CA229697Susan G. Komen CCR19608826
6 · The paper itself

Abstract

backgroundBreast cancer is a highly heterogeneous disease characterized by multiple histologic and molecular subtypes. While a myriad of breast cancer cell lines have been developed over the past 60 years, estrogen receptor alpha (ER)+ disease and some mutations associated with this subtype remain underrepresented. Here we describe six breast cancer cell lines derived from patient-derived xenografts (PDX) and their general characteristics.

methodsEstablished breast cancer PDX were processed into cell suspensions and placed into standard 2D cell culture; six emerged into long-term passageable cell lines. Cell lines were assessed for protein expression of common luminal, basal, and mesenchymal markers, growth assessed in response to estrogens and endocrine therapies, and RNA-seq and oncogenomics testing performed to compare relative transcript levels and identify putative oncogenic drivers.

resultsThree cell lines express ER and two are also progesterone receptor (PR) positive; PAM50 subtyping identified one line as luminal A. One of the ER+PR+ lines harbors a D538G mutation in the gene for ER (ESR1), providing a natural model that contains this endocrine-resistant genotype. The third ER+PR

conclusionsThese new generation breast cancer cell lines add to the existing repository of breast cancer models, increase the number of ER+ lines, and provide a resource that can be genetically modified for studying several important clinical breast cancer features.

Indexed as

Cell Line, TumorAnimalsBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularCell Culture TechniquesErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingHeterograftsHumansMiceMice, Inbred NODMice, SCIDReceptors, EstrogenReceptors, ProgesteroneErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneBreast cancerBreast cancer cell linesBreast cancer subtypesEstrogen receptorPatient-derived xenografts

Identifiers

PMID32576280
PMCPMC7310532
OpenAlexW3036668765

What OpenQuestion holds

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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.