Evidence map›Paper›PMID 42879033›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Epigenetic Analysis in Ewing Sarcoma.

Ornella Urzì, Tamina Stelzer, Jason Sims, Eleni M Tomazou

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2027. 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

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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.

No citing paper in PubMed yet.

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

4 authors.

Ornella UrzìSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Tamina StelzerSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Jason SimsSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Eleni M TomazouSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. eleni.tomazou@ccri.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ewing sarcoma is a malignant tumor of bone and soft tissue, primarily driven by the EWSR1::FLI1 fusion oncogene. This chimeric transcription factor reprograms gene regulatory networks by aberrantly activating enhancers and binding to GGAA microsatellite repeats, thereby reshaping the epigenetic landscape of tumor cells. Given that chromatin accessibility governs transcription factor binding and downstream gene expression, high-resolution mapping of protein-DNA interactions is critical for elucidating the epigenetic mechanisms underlying Ewing sarcoma pathogenesis. This chapter presents a comprehensive, end-to-end framework for the analysis of Cleavage Under Targets and Release Using Nuclease (CUT&RUN) data, with a focus on profiling EWSR1::FLI1 binding sites and their associated chromatin features. We detail each step of the analytical pipeline, including raw FASTQ processing, alignment, quality control, peak calling, and downstream analyses. To demonstrate the workflow, both publicly available data and data generated in our laboratory are used. Overall, this chapter serves as a practical and detailed methodological guide for researchers aiming to dissect the epigenetic architecture of Ewing sarcoma using CUT&RUN technology.

Indexed as

Bone NeoplasmsEpigenesis, GeneticEpigenomicsSarcoma, EwingBinding SitesChromatinGene Expression Regulation, NeoplasticHumansOncogene Proteins, FusionProto-Oncogene Protein c-fli-1RNA-Binding Protein EWSChromatinOncogene Proteins, FusionProto-Oncogene Protein c-fli-1RNA-Binding Protein EWSBioinformaticsCUT&RUNEpigeneticsEwing sarcomaEWSR1::FLI1

Identifiers

What OpenQuestion holds

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Registered trials

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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.