Evidence map›Paper›PMID 36243775›Full record

ArticleScientific data2022

An interactive mass spectrometry atlas of histone posttranslational modifications in T-cell acute leukemia.

Lien Provez, Bart Van Puyvelde, Laura Corveleyn, Nina Demeulemeester, Sigrid Verhelst, Béatrice Lintermans, Simon Daled, Juliette Roels, Lieven Clement, Lennart Martens and 3 more

Abstract readDataset
In one paragraph

Article in Scientific data, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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.

Lien Provez *Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID 0000-0003-2236-2347
Bart Van Puyvelde *ProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium.ORCID 0000-0002-7368-1762
Laura Corveleyn *ProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Nina Demeulemeester *Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID 0000-0002-8290-2432
Sigrid VerhelstProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Béatrice LintermansDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Simon DaledProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Juliette RoelsDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Lieven ClementDepartment of Applied Mathematics, Computer science and Statistics, Ghent University, Ghent, Belgium.
Lennart MartensDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID 0000-0003-4277-658X
Dieter DeforceProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Pieter Van Vlierberghe *Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Maarten Dhaenens *ProGenTomics, Laboratory of Pharmaceutical Biotechnology, Department of Pharmaceutics, Ghent University, Ghent, Belgium. maarten.dhaenens@ugent.be.ORCID 0000-0002-9801-3509

Funding

Fonds Wetenschappelijk Onderzoek (Research Foundation Flanders) 11B4518NFonds Wetenschappelijk Onderzoek (Research Foundation Flanders) 12E9716NFonds Wetenschappelijk Onderzoek (Research Foundation Flanders) 1SF2622NFonds Wetenschappelijk Onderzoek (Research Foundation Flanders) 3S031319Fonds Wetenschappelijk Onderzoek (Research Foundation Flanders) G028821N
6 · The paper itself

Abstract

The holistic nature of omics studies makes them ideally suited to generate hypotheses on health and disease. Sequencing-based genomics and mass spectrometry (MS)-based proteomics are linked through epigenetic regulation mechanisms. However, epigenomics is currently mainly focused on DNA methylation status using sequencing technologies, while studying histone posttranslational modifications (hPTMs) using MS is lagging, partly because reuse of raw data is impractical. Yet, targeting hPTMs using epidrugs is an established promising research avenue in cancer treatment. Therefore, we here present the most comprehensive MS-based preprocessed hPTM atlas to date, including 21 T-cell acute lymphoblastic leukemia (T-ALL) cell lines. We present the data in an intuitive and browsable single licensed Progenesis QIP project and provide all essential quality metrics, allowing users to assess the quality of the data, edit individual peptides, try novel annotation algorithms and export both peptide and protein data for downstream analyses, exemplified by the PeptidoformViz tool. This data resource sets the stage for generalizing MS-based histone analysis and provides the first reusable histone dataset for epidrug development.

Indexed as

HistonesLeukemiaEpigenesis, GeneticHumansMass SpectrometryPeptidesPrecursor T-Cell Lymphoblastic Leukemia-LymphomaProtein Processing, Post-TranslationalT-LymphocytesHistonesPeptides

Identifiers

PMID36243775
PMCPMC9569336

What Socratic 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 Socratic graph.