Evidence map›Paper›PMID 30992305›Full record

ArticleMolecular cancer research : MCR2019

Dual TGFβ/BMP Pathway Inhibition Enables Expansion and Characterization of Multiple Epithelial Cell Types of the Normal and Cancerous Breast.

Mayuri Prasad, Brijesh Kumar, Poornima Bhat-Nakshatri, Manjushree Anjanappa, George Sandusky, Kathy D Miller, Anna Maria Storniolo, Harikrishna Nakshatri

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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

8 authors at 3 institutions in 1 country.

Mayuri Prasad *Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Brijesh Kumar *Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Poornima Bhat-NakshatriDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Manjushree AnjanappaDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
George SanduskyDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Kathy D MillerDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Anna Maria StornioloDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Harikrishna NakshatriDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana. hnakshat@iupui.edu.
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USRichard 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

Functional modeling of normal breast epithelial hierarchy and stromal-epithelial cell interactions have been difficult due to inability to obtain sufficient stem-progenitor-mature epithelial and stromal cells. Recently reported epithelial reprogramming assay has partially overcome this limitation, but cross-contamination of cells from the feeder layer is a concern. The purpose of this study was to develop a feeder-layer-independent and inexpensive method to propagate multiple cell types from limited tissue resources. Cells obtained after enzymatic digestion of tissues collected at surgery or by core-needle biopsies were plated on tissue culture dishes precoated with laminin-5-rich-conditioned media from the rat bladder tumor cell line 804G and a defined growth media with inhibitors of ROCK, TGFβ, and BMP signaling. Cells were characterized by flow cytometry, mammosphere assay, 3D cultures, and xenograft studies. Cells from the healthy breasts included CD10

Indexed as

5'-NucleotidaseAnimalsAntigens, NeoplasmBreastBreast NeoplasmsCell DifferentiationCell LineageEpithelial Cell Adhesion MoleculeEpithelial CellsFemaleFlow CytometryGene Expression Regulation, NeoplasticHumansIntegrin alpha6MiceNeprilysin5'-NucleotidaseAntigens, NeoplasmEpithelial Cell Adhesion MoleculeIntegrin alpha6NeprilysinTransforming Growth Factor beta

Identifiers

PMID30992305
PMCPMC6610652
OpenAlexW2939132826

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.