Evidence map›Paper›PMID 29997232›Full record

ArticleCancer research2018

Normal Breast-Derived Epithelial Cells with Luminal and Intrinsic Subtype-Enriched Gene Expression Document Interindividual Differences in Their Differentiation Cascade.

Brijesh Kumar, Mayuri Prasad, Poornima Bhat-Nakshatri, Manjushree Anjanappa, Maitri Kalra, Natascia Marino, Anna Maria Storniolo, Xi Rao, Sheng Liu, Jun Wan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 58 citations in OpenAlex.

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  18. Oncotarget · 2022
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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

12 authors at 3 institutions in 1 country.

Brijesh Kumar *Departments of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Mayuri Prasad *Departments of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Poornima Bhat-NakshatriDepartments of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Manjushree AnjanappaDepartments of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Maitri KalraDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0002-6635-6152
Natascia MarinoDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Anna Maria StornioloDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Xi RaoDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Sheng LiuDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Jun WanDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Yunlong LiuDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Harikrishna NakshatriDepartments of Surgery, Indiana University School of Medicine, Indianapolis, Indiana. hnakshat@iupui.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineRichard L. Roudebush VA Medical Center · US

Funding

Estrogen-Estrogen Receptor axis in non-transformed breast epithelial cells: studies beyond MCF-7R03CA195250 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI NAKSHATRI, HARIKRISHNA · 2016 to 2017
$156k
NCI NIH HHS R03 CA195250
6 · The paper itself

Abstract

Cell-type origin is one of the factors that determine molecular features of tumors, but resources to validate this concept are scarce because of technical difficulties in propagating major cell types of adult organs. Previous attempts to generate such resources to study breast cancer have yielded predominantly basal-type cell lines. We have created a panel of immortalized cell lines from core breast biopsies of ancestry-mapped healthy women that form ductal structures similar to normal breast in 3D cultures and expressed markers of major cell types, including the luminal-differentiated cell-enriched ERα-FOXA1-GATA3 transcription factor network. We have also created cell lines from PROCR (CD201)

Indexed as

AdultBreastBreast NeoplasmsBromodomain Containing ProteinsCell Cycle ProteinsCell DifferentiationCell LineageEndothelial Protein C ReceptorEpithelial Cell Adhesion MoleculeEpithelial CellsEstrogen Receptor alphaFemaleGATA3 Transcription FactorGene Expression Regulation, NeoplasticHepatocyte Nuclear Factor 3-alphaHigh-Throughput Nucleotide SequencingAKT2 protein, humanBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsEndothelial Protein C ReceptorEPCAM protein, humanEpithelial Cell Adhesion MoleculeESR1 protein, humanEstrogen Receptor alphaFOXA1 protein, humanGATA3 protein, humanGATA3 Transcription FactorHepatocyte Nuclear Factor 3-alphaNF-kappa BNuclear ProteinsPROCR protein, humanProto-Oncogene Proteins c-aktTranscription Factors

Identifiers

PMID29997232
PMCPMC6125218
OpenAlexW2829837434

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.