Evidence map›Paper›PMID 32747535›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells.

Evelyn Susanto, Ana Marin Navarro, Leilei Zhou, Anders Sundström, Niek van Bree, Marina Stantic, Mohsen Moslem, Jignesh Tailor, Jonne Rietdijk, Veronica Zubillaga and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Modeling pediatric brain tumors with human stem cells.Frontiers in cellular neuroscience · 2026
    Review
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  20. Modeling Brain Tumors: A Perspective Overview ofFrontiers in molecular neuroscience · 2022
    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

24 authors at 7 institutions in 4 countries.

Evelyn SusantoDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Ana Marin NavarroDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Leilei ZhouDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Anders SundströmDepartment of Immunology, Genetics, and Pathology, Science For Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.ORCID 0000-0003-3942-6271
Niek van BreeDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.ORCID 0000-0001-5010-3524
Marina StanticDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Mohsen MoslemDepartment of Neuroscience, Karolinska Institutet, 171 65 Stockholm, Sweden.ORCID 0000-0002-2440-9586
Jignesh TailorDevelopmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Jonne RietdijkDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Veronica ZubillagaDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.ORCID 0000-0002-8806-939X
Jens-Martin HübnerHopp Children's Cancer Center (KiTZ), 69120 Heidelberg, Germany.
Holger WeishauptDepartment of Immunology, Genetics, and Pathology, Science For Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Johanna WolfsbergerDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden.
Irina AlafuzoffDepartment of Immunology, Genetics, and Pathology, Science For Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.ORCID 0000-0002-6249-569X
Ann NordgrenDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.
Thierry MagnaldoInstitute for Research on Cancer and Aging, CNRS UMR 7284, INSERM U1081, University of Nice Sophia Antipolis, Nice, France.ORCID 0000-0001-9174-8599
Peter SiesjöDivision of Neurosurgery, Department of Clinical Sciences, Skane University Hospital, 221 85 Lund, Sweden.
John Inge JohnsenDepartment of Women's and Children's Health, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0003-1277-812X
Marcel KoolHopp Children's Cancer Center (KiTZ), 69120 Heidelberg, Germany.ORCID 0000-0002-6557-5468
Kristiina TammimiesDepartment of Women's and Children's Health, Karolinska Institutet, 171 76 Stockholm, Sweden.ORCID 0000-0002-8324-4697
Anna DarabiGlioma Immunotherapy Group, Division of Neurosurgery, Department of Clinical Sciences, Lund University, 221 85 Lund, Sweden.ORCID 0000-0003-4326-8149
Fredrik J SwartlingDepartment of Immunology, Genetics, and Pathology, Science For Life Laboratory, Uppsala University, 751 85 Uppsala, Sweden.ORCID 0000-0002-8460-4367
Anna FalkDepartment of Neuroscience, Karolinska Institutet, 171 65 Stockholm, Sweden; margareta.wilhelm@ki.se anna.falk@ki.se.ORCID 0000-0003-1634-8610
Margareta WilhelmDepartment of Microbiology, Tumor and Cell biology (MTC), Karolinska Institutet, 171 65 Stockholm, Sweden; margareta.wilhelm@ki.se anna.falk@ki.se.ORCID 0000-0002-0516-9724
Karolinska Institutet · SEUppsala University · SEGerman Cancer Research Center · DELund University · SECentre National de la Recherche Scientifique · FRKarolinska University Hospital · SEUniversity of Toronto · CA

Funding

Wellcome Trust 201511/Z/16/Z
6 · The paper itself

Abstract

Medulloblastoma is the most common malignant brain tumor in children. Here we describe a medulloblastoma model using Induced pluripotent stem (iPS) cell-derived human neuroepithelial stem (NES) cells generated from a Gorlin syndrome patient carrying a germline mutation in the sonic hedgehog (SHH) receptor

Indexed as

AnilidesAnimalsBasal Cell Nevus SyndromeCell Line, TumorCell ProliferationGalectin 1Gene Expression Regulation, NeoplasticHedgehog ProteinsHumansMedulloblastomaMiceNeoplasms, ExperimentalNeural Stem CellsPatched-1 ReceptorPyridinesAnilidesGalectin 1Hedgehog ProteinsHhAntag691Patched-1 ReceptorPTCH1 protein, humanPyridinesSHH protein, humandisease modelmedulloblastomaneural stem cells

Identifiers

PMID32747535
PMCPMC7443968
OpenAlexW3047007133

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.