Evidence map›Paper›PMID 33712610›Full record

ArticleNature communications2021

Schwann cell plasticity regulates neuroblastic tumor cell differentiation via epidermal growth factor-like protein 8.

Tamara Weiss, Sabine Taschner-Mandl, Lukas Janker, Andrea Bileck, Fikret Rifatbegovic, Florian Kromp, Helena Sorger, Maximilian O Kauer, Christian Frech, Reinhard Windhager and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 88 citations in OpenAlex.

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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 3 institutions in 2 countries.

Tamara Weiss *St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0001-7046-3412
Sabine Taschner-Mandl *St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. sabine.taschner@ccri.at.ORCID http://orcid.org/0000-0002-1439-5301
Lukas JankerDepartment of Analytical Chemistry, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-3084-2212
Andrea BileckDepartment of Analytical Chemistry, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-7053-8856
Fikret RifatbegovicSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0002-9956-2382
Florian KrompSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0003-4557-5652
Helena SorgerSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.ORCID http://orcid.org/0000-0002-3380-7770
Maximilian O KauerSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Christian FrechSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Reinhard WindhagerDepartment of Orthopedic Surgery, Medical University of Vienna, Vienna, Austria.
Christopher GernerDepartment of Analytical Chemistry, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-4964-0642
Peter F AmbrosSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Inge M AmbrosSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
St Anna Children's Hospital · ATUniversity of Vienna · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult Schwann cells (SCs) possess an inherent plastic potential. This plasticity allows SCs to acquire repair-specific functions essential for peripheral nerve regeneration. Here, we investigate whether stromal SCs in benign-behaving peripheral neuroblastic tumors adopt a similar cellular state. We profile ganglioneuromas and neuroblastomas, rich and poor in SC stroma, respectively, and peripheral nerves after injury, rich in repair SCs. Indeed, stromal SCs in ganglioneuromas and repair SCs share the expression of nerve repair-associated genes. Neuroblastoma cells, derived from aggressive tumors, respond to primary repair-related SCs and their secretome with increased neuronal differentiation and reduced proliferation. Within the pool of secreted stromal and repair SC factors, we identify EGFL8, a matricellular protein with so far undescribed function, to act as neuritogen and to rewire cellular signaling by activating kinases involved in neurogenesis. In summary, we report that human SCs undergo a similar adaptive response in two patho-physiologically distinct situations, peripheral nerve injury and tumor development.

Indexed as

AdolescentAdultAgedAged, 80 and overCalcium-Binding ProteinsCell DifferentiationCell LineCell PlasticityCell ProliferationCoculture TechniquesEGF Family of ProteinsFemaleHumansMaleMiddle AgedNerve RegenerationCalcium-Binding ProteinsEGF Family of ProteinsEGFL8 protein, human

Identifiers

PMID33712610
PMCPMC7954855
OpenAlexW3133837583

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.