Evidence map›Paper›PMID 37365178›Full record

ArticleNature communications2023

Single-cell transcriptomics and epigenomics unravel the role of monocytes in neuroblastoma bone marrow metastasis.

Irfete S Fetahu, Wolfgang Esser-Skala, Rohit Dnyansagar, Samuel Sindelar, Fikret Rifatbegovic, Andrea Bileck, Lukas Skos, Eva Bozsaky, Daria Lazic, Lisa Shaw and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.9field-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

44 citing papers in PubMed, 49 citations in OpenAlex.

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  3. Single-Cell Analysis Reveals the Soft Tissue Structure Heterogeneity Aggravates Peri-Implantitis Through MDK Signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

22 authors at 6 institutions in 3 countries.

Irfete S Fetahu *St. Anna Children's Cancer Research Institute, Vienna, Austria. irfete.fetahu@ccri.at.ORCID 0000-0002-0468-7458
Wolfgang Esser-Skala *Department of Biosciences and Medical Biology, University of Salzburg, Salzburg, Austria.
Rohit Dnyansagar *Department of Biosciences and Medical Biology, University of Salzburg, Salzburg, Austria.
Samuel SindelarDepartment of Biosciences and Medical Biology, University of Salzburg, Salzburg, Austria.
Fikret RifatbegovicSt. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID 0000-0002-9956-2382
Andrea BileckUniversity of Vienna, Department of Analytical Chemistry, Faculty of Chemistry, Vienna, Austria.ORCID 0000-0002-7053-8856
Lukas SkosUniversity of Vienna, Department of Analytical Chemistry, Faculty of Chemistry, Vienna, Austria.ORCID 0000-0003-3983-1736
Eva BozsakySt. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID 0000-0001-6208-368X
Daria LazicSt. Anna Children's Cancer Research Institute, Vienna, Austria.
Lisa ShawMedical University of Vienna, Department of Dermatology, Vienna, Austria.ORCID 0000-0003-2273-7655
Marcus TötzlSt. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID 0000-0003-0321-5835
Dora TarlungeanuSt. Anna Children's Cancer Research Institute, Vienna, Austria.
Marie BernkopfSt. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID 0000-0001-6650-4592
Magdalena RadosSt. Anna Children's Cancer Research Institute, Vienna, Austria.
Wolfgang WeningerMedical University of Vienna, Department of Dermatology, Vienna, Austria.
Eleni M TomazouSt. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID 0000-0002-7497-4567
Christoph BockCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0001-6091-3088
Christopher GernerUniversity of Vienna, Department of Analytical Chemistry, Faculty of Chemistry, Vienna, Austria.ORCID 0000-0003-4964-0642
Ruth LadensteinSt. Anna Children's Hospital and St. Anna Children's Cancer Research Institute, Department of Studies and Statistics for Integrated Research and Projects, Vienna, Austria.ORCID 0000-0001-6548-3873
Matthias FarlikMedical University of Vienna, Department of Dermatology, Vienna, Austria.ORCID 0000-0003-0698-2992
Nikolaus FortelnyDepartment of Biosciences and Medical Biology, University of Salzburg, Salzburg, Austria. nikolaus.fortelny@plus.ac.at.ORCID 0000-0003-4025-9968
Sabine Taschner-MandlSt. Anna Children's Cancer Research Institute, Vienna, Austria. sabine.taschner@ccri.at.ORCID 0000-0002-1439-5301
St Anna Children's Hospital · ATUniversity of Salzburg · ATMedical University of Vienna · ATUniversity of Vienna · ATAustrian Academy of Sciences · ATCancer Research Institute of the Slovak Academy of Sciences · SK

Funding

Austrian Science Fund FWF I 4162Austrian Science Fund FWF P 34958Austrian Science Fund FWF P 35072Austrian Science Fund FWF P 35841Austrian Science Fund FWF TAI 592
6 · The paper itself

Abstract

Metastasis is the major cause of cancer-related deaths. Neuroblastoma (NB), a childhood tumor has been molecularly defined at the primary cancer site, however, the bone marrow (BM) as the metastatic niche of NB is poorly characterized. Here we perform single-cell transcriptomic and epigenomic profiling of BM aspirates from 11 subjects spanning three major NB subtypes and compare these to five age-matched and metastasis-free BM, followed by in-depth single cell analyses of tissue diversity and cell-cell interactions, as well as functional validation. We show that cellular plasticity of NB tumor cells is conserved upon metastasis and tumor cell type composition is NB subtype-dependent. NB cells signal to the BM microenvironment, rewiring via macrophage mgration inhibitory factor and midkine signaling specifically monocytes, which exhibit M1 and M2 features, are marked by activation of pro- and anti-inflammatory programs, and express tumor-promoting factors, reminiscent of tumor-associated macrophages. The interactions and pathways characterized in our study provide the basis for therapeutic approaches that target tumor-to-microenvironment interactions.

Indexed as

Bone Marrow NeoplasmsNeuroblastomaBone MarrowChildEpigenomicsHumansMonocytesTranscriptomeTumor Microenvironment

Identifiers

PMID37365178
PMCPMC10293285
OpenAlexW4382060415

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.