Evidence map›Paper›PMID 30286804›Full record

ArticleStem cell research & therapy2018

A robust cell culture system for large scale feeder cell-free expansion of human breast epithelial progenitors.

Sumanta Chatterjee, Pratima Basak, Edward Buchel, Leigh C Murphy, Afshin Raouf

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Towards organoid culture without Matrigel.Communications biology · 2021
    Review
  4. Organoids as ComplexCellular and molecular bioengineering · 2020
    Review
  5. 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

5 authors.

Sumanta ChatterjeeDepartment of Immunology, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, R3E 0T5, Canada.
Pratima BasakDepartment of Immunology, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, R3E 0T5, Canada.
Edward BuchelDepartment of Surgery, Section of Plastic Surgery, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, R3A 1M5, Canada.
Leigh C MurphyResearch Institute of Oncology & Hematology, CancerCare Manitoba, Winnipeg, MB, R3E 0V9, Canada.
Afshin RaoufDepartment of Immunology, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, R3E 0T5, Canada. Afshin.Raouf@umanitoba.ca.ORCID 0000-0002-9188-7537

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNormal human breast epithelial cells are maintained by the proliferation and differentiation of different human breast epithelial progenitors (HBEPs). However, these progenitor subsets can only be obtained at low frequencies, limiting their further characterization. Recently, it was reported that HBEPs can be minimally expanded in Matrigel cocultures with stromal feeder cells. However, variability of generating healthy feeder cells significantly impacts the effective expansion of HBEPs.

methodsHere, we report a robust feeder cell-free culture system for large-scale expansion of HBEPs in two-dimensional cultures.

resultsUsing this cell culture system HBEPs can be exponentially expanded as bulk cultures. Moreover, purified HBEP subtypes can also be separately expanded using our cell culture system. The expanded HBEPs retain their undifferentiated phenotype and form distinct epithelial colonies in colony forming cell assays.

conclusionsThe availability of a culture system enabling the large-scale expansion of HBEPs facilitates their application to screening platforms and other cell-based assays.

Indexed as

Antigens, CDBiomarkersCadherinsCell ProliferationCoculture TechniquesCollagenColony-Forming Units AssayDrug CombinationsEpithelial CellsEpithelial-Mesenchymal TransitionEstrogen Receptor alphaFeeder CellsFemaleGene ExpressionHumansInterleukin-10Antigens, CDBiomarkersCadherinsCDH1 protein, humanCDH2 protein, humanCollagenDrug CombinationsESR1 protein, humanEstrogen Receptor alphaIL10 protein, humanInterleukin-10Keratin-19KRT19 protein, humanLamininmatrigelProteoglycans

Identifiers

PMID30286804
PMCPMC6172804

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Registered trials

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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.