Evidence map›Paper›PMID 37090655›Full record

ArticlebioRxiv : the preprint server for biology2023

Carcinoma-associated fibroblast-like tumor cells remodel the Ewing sarcoma tumor microenvironment.

Emma D Wrenn, April A Apfelbaum, Erin R Rudzinski, Xuemei Deng, Wei Jiang, Sudha Sud, Raelene A Van Noord, Erika A Newman, Nicolas M Garcia, Virginia J Hoglund and 5 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 1 country.

Emma D WrennBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
April A ApfelbaumBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
Erin R RudzinskiPathology Department, Seattle Children's Hospital, Seattle, Washington.
Xuemei DengPathology Department, Seattle Children's Hospital, Seattle, Washington.
Wei JiangRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Sudha SudRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Raelene A Van NoordRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Erika A NewmanRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.
Nicolas M GarciaBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
Virginia J HoglundBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
Shruti S BhiseClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Sami B KanaanClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Olivia G WaltnerClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Scott N FurlanClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Elizabeth R LawlorBen Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, WA.
Seattle Children's Hospital · USUniversity of Michigan · USFred Hutch Cancer Center · USUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Regulation and function of HOX genes in Ewing sarcoma pathogenesisR01CA215981 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAWLOR, ELIZABETH R · 2018 to 2022
$2.0M
The role of HOXD13 in controlling Ewing sarcoma cell plasticity and metastasisF31CA247104 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI APFELBAUM, APRIL · 2021 to 2022
$66k
NCI NIH HHS F31 CA247104NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA215981
6 · The paper itself

Abstract

Tumor heterogeneity is a major driver of cancer progression. In epithelial-derived malignancies, carcinoma-associated fibroblasts (CAFs) contribute to tumor heterogeneity by depositing extracellular matrix (ECM) proteins that dynamically remodel the tumor microenvironment (TME). Ewing sarcomas (EwS) are histologically monomorphous, mesenchyme-derived tumors that are devoid of CAFs. Here we identify a previously uncharacterized subpopulation of transcriptionally distinct EwS tumor cells that deposit pro-tumorigenic ECM. Single cell analyses revealed that these CAF-like cells differ from bulk EwS cells by their upregulation of a matrisome-rich gene signature that is normally repressed by EWS::FLI1, the oncogenic fusion transcription factor that underlies EwS pathogenesis. Further, our studies showed that ECM-depositing tumor cells express the cell surface marker CD73, allowing for their isolation ex vivo and detection in situ. Spatial profiling of tumor xenografts and patient biopsies demonstrated that CD73

Identifiers

PMID37090655
PMCPMC10120623
OpenAlexW4365445320

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.