Evidence map›Paper›PMID 32183367›Full record

ArticleCancers2020

A Comprehensive Molecular Characterization of the Pancreatic Neuroendocrine Tumor Cell Lines BON-1 and QGP-1.

Kim B Luley, Shauni B Biedermann, Axel Künstner, Hauke Busch, Sören Franzenburg, Jörg Schrader, Patricia Grabowski, Ulrich F Wellner, Tobias Keck, Georg Brabant and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-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

34 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Crinophagy in Pancreatic Beta Cells: From Insulin Granule Turnover to Diabetes Pathogenesis.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    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

13 authors at 6 institutions in 2 countries.

Kim B LuleyClinic for Hematology and Oncology, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Shauni B BiedermannFirst Department of Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Axel KünstnerGroup for Medical Systems Biology, Lübeck Institute of Experimental Dermatology, University of Lübeck, D-23538 Lübeck, Germany.ORCID 0000-0003-0692-2105
Hauke BuschGroup for Medical Systems Biology, Lübeck Institute of Experimental Dermatology, University of Lübeck, D-23538 Lübeck, Germany.ORCID 0000-0003-4763-4521
Sören FranzenburgInstitute for Clinical Molecular Biology, University of Kiel, Kiel, D-24105 Kiel, Germany.
Jörg SchraderFirst Medical Department-Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Patricia GrabowskiDepartment of Medical Immunology, Charité Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, D-13353 Berlin, Germany.
Ulrich F WellnerDepartment of Surgery, University Medical Center Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Tobias KeckDepartment of Surgery, University Medical Center Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Georg BrabantFirst Department of Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Sebastian M SchmidInstitute for Endocrinology and Diabetes, University of Lübeck, D-23538 Lübeck, Germany.
Hendrik LehnertFirst Department of Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.
Hendrik UngefrorenFirst Department of Medicine, University Hospital Schleswig-Holstein, Campus Lübeck, D-23538 Lübeck, Germany.ORCID 0000-0002-7552-2087
University of Lübeck · DEUniversity Hospital Schleswig-Holstein · DEChristian-Albrechts-Universität zu Kiel · DEHumboldt-Universität zu Berlin · DEUniversität Hamburg · DEUniversity of Salzburg · AT

Funding

Ipsen Pharma A_DE-52030-373
6 · The paper itself

Abstract

Experimental models of neuroendocrine tumor disease are scarce, with only a few existing neuroendocrine tumor cell lines of pancreatic origin (panNET). Their molecular characterization has so far focused on the neuroendocrine phenotype and cancer-related mutations, while a transcription-based assessment of their developmental origin and malignant potential is lacking. In this study, we performed immunoblotting and qPCR analysis of neuroendocrine, epithelial, developmental endocrine-related genes as well as next-generation sequencing (NGS) analysis of microRNAs (miRs) on three panNET cell lines, BON-1, QGP-1, and NT-3. All three lines displayed a neuroendocrine and epithelial phenotype; however, while insulinoma-derived NT-3 cells preferentially expressed markers of mature functional pancreatic β-cells (i.e.,

Indexed as

b-cellBON-1EMTmicroRNANT-3pancreatic neuroendocrine tumorQGP-1

Identifiers

PMID32183367
PMCPMC7140066
OpenAlexW3010714716

What Socratic 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 Socratic graph.