Evidence map›Paper›PMID 30621293›Full record

ArticleCells2019

Commonly Used Pancreatic Stellate Cell Cultures Differ Phenotypically and in Their Interactions with Pancreatic Cancer Cells.

Daniela Lenggenhager, Manoj Amrutkar, Petra Sántha, Monica Aasrum, Johannes-Matthias Löhr, Ivar P Gladhaug, Caroline S Verbeke

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Organoid technology for personalized pancreatic cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2021
    Review
  12. Review
  13. Review
  14. Pancreatic Ductal Adenocarcinoma: PreclinicalFrontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. Engineering of biomaterials for tumor modeling.Materials today. Advances · 2020
    Article
  17. Article
  18. Article
  19. Plasma Membrane CaCancers · 2020
    Article
  20. 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

7 authors at 3 institutions in 3 countries.

Daniela LenggenhagerDepartment of Pathology, Institute of Clinical Medicine, University of Oslo, Blindern, 0316 Oslo, Norway. Daniela.Lenggenhager@usz.ch.
Manoj AmrutkarDepartment of Pharmacology, Institute of Clinical Medicine, University of Oslo, Blindern, 0316 Oslo, Norway. manoj.amrutkar@medisin.uio.no.ORCID 0000-0002-1868-0249
Petra SánthaDepartment of Pathology, Oslo University Hospital Rikshospitalet, Nydalen, 0424 Oslo, Norway. petra.santha@medisin.uio.no.
Monica AasrumDepartment of Pharmacology, Institute of Clinical Medicine, University of Oslo, Blindern, 0316 Oslo, Norway. monica.aasrum@medisin.uio.no.
Johannes-Matthias LöhrDepartment of Clinical Science, Intervention and Technology, Karolinska Institutet, K 53, 141 86 Stockholm, Sweden. matthias.lohr@ki.se.ORCID 0000-0002-7647-198X
Ivar P GladhaugDepartment of Hepato-Pancreato-Biliary Surgery, Institute of Clinical Medicine, University of Oslo, P.O. Box 1171 Blindern, 0318 Oslo, Norway. i.p.gladhaug@medisin.uio.no.
Caroline S VerbekeDepartment of Pathology, Institute of Clinical Medicine, University of Oslo, Blindern, 0316 Oslo, Norway. c.s.verbeke@medisin.uio.no.ORCID 0000-0002-1111-9715
Oslo University Hospital · NOUniversity of Oslo · NOKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activated pancreatic stellate cells (PSCs) play a central role in the tumor stroma of pancreatic ductal adenocarcinoma (PDAC). Given the limited availability of patient-derived PSCs from PDAC, immortalized PSC cell lines of murine and human origin have been established; however, it is not elucidated whether differences in species, organ disease status, donor age, and immortalization alter the PSC phenotype and behavior compared to that of patient-derived primary PSC cultures. Therefore, a panel of commonly used PSC cultures was examined for important phenotypical and functional features: three primary cultures from human PDAC, one primary from normal human pancreas, and three immortalized (one from human, two from murine pancreas). Growth rate was considerably lower in primary PSCs from human PDAC. Basal collagen synthesis varied between the PSC cultures, and TGF-β stimulation increased collagen synthesis only in non-immortalized cultures. Differences in secretome composition were observed along with a divergence in the DNA synthesis, migration, and response to gemcitabine of PDAC cell lines that were grown in conditioned medium from the various PSC cultures. The findings reveal considerable differences in features and functions that are key to PSCs and in the interactions with PDAC. These observations may be relevant to researchers when selecting the most appropriate PSC culture for their experiments.

Indexed as

AnimalsCarcinoma, Pancreatic DuctalCell Line, TumorCell MovementCell ProliferationCollagenHumansPancreatic Stellate CellsPhenotypeTransforming Growth Factor betaCollagenTransforming Growth Factor betapancreatic cancerpancreatic stellate cellsTGF-βtumor-stroma interaction

Identifiers

PMID30621293
PMCPMC6356867
OpenAlexW2908458492

What OpenQuestion holds

Textmetadata
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.