PXD067935 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Profiling histone post-translational modifications to identify signatures of epigenetic drug response in T-cell acute lymphoblastic leukemia |
| Description | Epigenetic modifications are dynamic and reversible, making them attractive targets for therapeutic intervention in cancer. Although several epigenetic drugs (epidrugs) have been clinically approved, their application in T-cell acute lymphoblastic leukemia (T-ALL) remains limited, and predictive biomarkers of response are lacking. Here, we present a mass spectrometry (MS)-based pharmacoepigenetic approach to profile histone post-translational modifications (hPTMs) to identify signatures associated with epidrug sensitivity in T-ALL. Baseline hPTM landscapes were previously established by our group for 21 T-ALL cell lines using liquid chromatography–tandem mass spectrometry (LC–MS/MS). Here, we treated these cell lines with a panel of nine epidrugs including anthracyclines, histone deacetylase inhibitors, and DNA methyltransferase inhibitors. Correlation of cell viability data with hPTM levels revealed distinct hPTM signatures linked to sensitivity for each drug class. These signatures were subsequently evaluated in T-ALL patient-derived xenograft (PDX) models. However, we our analysis revealed substantial discepancies in hPTM sensitivity signatures compared to those observed in vitro. Co-variation network analysis highlighted divergence in hPTM-hPTM correlation between the two models, underscoring limitations of cell lines for modeling dynamic epigenetic regulation in vivo. Our findings establish a framework for MS-based hPTM profiling in T-ALL and emphasize the importance of model selection in developing predictive epigenetic biomarkers. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-06-08 |
| AnnouncementXML | Submission_2026-06-07_16:29:15.896.xml |
| DigitalObjectIdentifier | https://doi.org/10.6019/PXD067935 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Laura Corveleyn |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | monomethylated residue; phosphorylated residue; acetylated residue; formylated residue |
| Instrument | ZenoTOF 7600 |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-09-01 02:01:29 | ID requested | |
| ⏵ 1 | 2026-06-07 16:29:16 | announced | |
Publication List
| 10.1038/s41598-026-44665-4; |
| 10.6019/PXD067935; |
| Corveleyn L, Provez L, Satilmis O, Refhagen N, Landfors M, Sleeckx W, Lintermans B, De Maesschalck A, Kotecha RS, De Moerloose B, Lammens T, Deforce D, Degerman S, Goossens S, Van Vlierberghe P, Dhaenens M, Profiling histone post-translational modifications to identify signatures of epigenetic drug response in T-cell acute lymphoblastic leukemia. Sci Rep, 16(1):(2026) [pubmed] |
Keyword List
| submitter keyword: histone post-translational modifications, LC-MS, pharmacoepigenetics,Epigenetics, T-ALL |
Contact List
| Maarten Dhaenens |
| contact affiliation | ProGenTomics Laboratory of Pharmaceutical Biotechnology, Ghent University, Belgium |
| contact email | maarten.dhaenens@ugent.be |
| lab head | |
| Laura Corveleyn |
| contact affiliation | ProGenTomics, Ghent University |
| contact email | lcorvele@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD067935
- Label: PRIDE project
- Name: Profiling histone post-translational modifications to identify signatures of epigenetic drug response in T-cell acute lymphoblastic leukemia