Evidence map›Paper›PMID 33767450›Full record

ArticleNature genetics2021

Single-cell transcriptomic analyses provide insights into the developmental origins of neuroblastoma.

Selina Jansky, Ashwini Kumar Sharma, Verena Körber, Andrés Quintero, Umut H Toprak, Elisa M Wecht, Moritz Gartlgruber, Alessandro Greco, Elad Chomsky, Thomas G P Grünewald and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 196 papers.

0numbers the graph read from it
0cells of the map it votes in
196citing papers in PubMed
26.6field-weighted citation impact, top 1% 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

196 citing papers in PubMed, 296 citations in OpenAlex.

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  15. Modern Mining: The Role of Single-cell RNA Sequencing in Advancing Neuroscience Research.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
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136 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Selina JanskyHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.ORCID http://orcid.org/0000-0003-4227-0298
Ashwini Kumar SharmaHealth Data Science Unit, Medical Faculty University Heidelberg and BioQuant, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-7883-7888
Verena KörberDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Andrés QuinteroFaculty of Biosciences, Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-3959-805X
Umut H ToprakHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Elisa M WechtHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Moritz GartlgruberHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Alessandro GrecoFaculty of Biosciences, Heidelberg University, Heidelberg, Germany.
Elad ChomskyDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Thomas G P GrünewaldHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.ORCID http://orcid.org/0000-0003-0920-7377
Kai-Oliver HenrichHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Amos TanayDepartment of Computer Science and Applied Mathematics and Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.ORCID http://orcid.org/0000-0001-9419-3824
Carl HerrmannHealth Data Science Unit, Medical Faculty University Heidelberg and BioQuant, Heidelberg, Germany.
Thomas HöferDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3560-8780
Frank WestermannHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany. f.westermann@kitz-heidelberg.de.ORCID http://orcid.org/0000-0003-1584-3636
German Cancer Research Center · DEHeidelberg University · DEWeizmann Institute of Science · IL

Funding

Medical Research Council MR/R006237/1
6 · The paper itself

Abstract

Neuroblastoma is a pediatric tumor of the developing sympathetic nervous system. However, the cellular origin of neuroblastoma has yet to be defined. Here we studied the single-cell transcriptomes of neuroblastomas and normal human developing adrenal glands at various stages of embryonic and fetal development. We defined normal differentiation trajectories from Schwann cell precursors over intermediate states to neuroblasts or chromaffin cells and showed that neuroblastomas transcriptionally resemble normal fetal adrenal neuroblasts. Importantly, neuroblastomas with varying clinical phenotypes matched different temporal states along normal neuroblast differentiation trajectories, with the degree of differentiation corresponding to clinical prognosis. Our work highlights the roles of oncogenic MYCN and loss of TFAP2B in blocking differentiation and may provide the basis for designing therapeutic interventions to overcome differentiation blocks.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisAdrenal GlandsCell DifferentiationCell Line, TumorCohort StudiesGene Expression Regulation, NeoplasticHumansNeuroblastomaTranscriptomeTreatment Outcome

Identifiers

PMID33767450
OpenAlexW3137366663

What OpenQuestion holds

Textmetadata
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.