Evidence map›Paper›PMID 29055717›Full record

ArticleExperimental neurology2018

Development of 3D culture models of plexiform neurofibroma and initial application for phenotypic characterization and drug screening.

Janice M Kraniak, Anita Chalasani, Margaret R Wallace, Raymond R Mattingly

Abstract read
In one paragraph

Article in Experimental neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Emerging therapeutic targets for neurofibromatosis type 1.Expert opinion on therapeutic targets · 2018
    Review
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

4 authors at 2 institutions in 1 country.

Janice M KraniakDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: ac0377@wayne.edu.
Anita ChalasaniDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: ag6370@wayne.edu.
Margaret R WallaceDepartment of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL, USA; University of Florida Health Cancer Center, University of Florida, Gainesville, FL, USA; University of Florida Genetics Institute, University of Florida, Gainesville, FL, USA. Electronic address: peggyw@mgm.ufl.edu.
Raymond R MattinglyDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA; Department of Oncology, Wayne State University and Karmanos Cancer Institute, Detroit, MI, USA. Electronic address: r.mattingly@wayne.edu.
Wayne State University · USFlorida College · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

Plexiform neurofibromas (PNs), which may be present at birth in up to half of children with type 1 neurofibromatosis (NF1), can cause serious loss of function, such as quadriparesis, and can undergo malignant transformation. Surgery is the first line treatment although the invasive nature of these tumors often prevents complete resection. Recent clinical trials have shown promising success for some drugs, notably selumetinib, an inhibitor of MAP kinase kinase (MEK). We have developed three-dimensional (3D) cell culture models of immortalized cells from NF1 PNs and of control Schwann cells (SCs) that we believe mimic more closely the in vivo condition than conventional two-dimensional (2D) cell culture. Our goal is to facilitate pre-clinical identification of potential targeted therapeutics for these tumors. Three drugs, selumetinib (a MEK inhibitor), picropodophyllin (an IGF-1R inhibitor) and LDN-193189 (a BMP2 inhibitor) were tested with dose-response design in both 2D and 3D cultures for their abilities to block net cell growth. Cell lines grown in 3D conditions showed varying degrees of resistance to the inhibitory actions of all three drugs. For example, control SCs became resistant to growth inhibition by selumetinib in 3D culture. LDN-193189 was the most effective drug in 3D cultures, with only slightly reduced potency compared to the 2D cultures. Characterization of these models also demonstrated increased proteolysis of collagen IV in the matrix by the PN driver cells as compared to wild-type SCs. The proteolytic capacity of the PN cells in the model may be a clinically significant property that can be used for testing the ability of drugs to inhibit their invasive phenotype.

Indexed as

Cell Culture TechniquesAntineoplastic AgentsBenzimidazolesBone Morphogenetic Protein 2Cells, CulturedDose-Response Relationship, DrugDrug Resistance, NeoplasmDrug Screening Assays, AntitumorGenes, Neurofibromatosis 1Genes, ReporterHumansLuminescent ProteinsMAP Kinase Kinase 1Molecular Targeted TherapyNeurofibroma, PlexiformNeurofibromatosis 1Antineoplastic AgentsAZD 6244BenzimidazolesBMP2 protein, humanBone Morphogenetic Protein 2LDN 193189Luminescent ProteinsMAP Kinase Kinase 1picropodophyllinPodophyllotoxinProtein Kinase InhibitorsPyrazolesPyrimidinesReceptor, IGF Type 1Red Fluorescent Protein3D culture modelMatrix proteolysisNF1Plexiform neurofibromaTargeted therapeutics

Identifiers

PMID29055717
PMCPMC6863155
OpenAlexW2766830321

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.