PXD015151 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Histone Modification Analysis of Oligodendroglioma and Astrocytoma Brain Cancer Samples |
Description | WHO classification for tumors of the central nervous system strongly endorses molecular tests for the precise diagnosis of diffuse gliomas. While alterations in the DNA methylation status of gliomas are already well documented and used in specialised clinical centers to distinguish between brain tumor entities, changes to the epigenetic layer at the level of histone modifications are only poorly characterised. Here, we applied a recently developed data-independent acquisition (DIA) - mass spectrometry method to generate a comprehensive histone epi-proteomic map that documents the abundance of almost all characterized and many uncharacterized histone modifications to a series of IDH-mutant oligodendroglioma and astrocytoma samples. Our analysis documented significant abundance differences in almost one-third of the 144 quantified histone peptides. Among them are lower abundance levels of the polycomb repressive mark H3K27me3 in oligodendroglioma samples compared to astrocytomas. We validated this finding by immunohistochemistry using the C36B11 antibody. Surprisingly, we observed inconsistencies with another widely applied H3K27me3 antibody (07-449), providing a warning flag for immunohistochemistry of brain cancers. An unbiased unsupervised clustering analysis of the proteomic dataset separated the two IDH-mutant glioma subtypes in full accordance to the EPIC DNA methylation classifier and the 1p/19q status. The clustering also revealed at least two histone epi-proteomic subgroups of oligodendroglioma, a feature not observable in the DNA methylation dataset. Our results indicate that histone epi-proteomic profiling at the depth of the current method has the capacity to identify clinically-relevant glioma sub-groups. In addition to being of use for diagnostic purposes, this could also provide novel insights in glioma biology and may identify new therapeutic targets. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-22 |
AnnouncementXML | Submission_2024-10-22_04:57:39.358.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Christian Feller |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | monomethylated residue; phosphorylated residue; acetylated residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2019-08-25 23:54:03 | ID requested | |
1 | 2020-01-17 05:41:01 | announced | |
⏵ 2 | 2024-10-22 04:57:45 | announced | 2024-10-22: Updated project metadata. |
Publication List
Feller C, Felix M, Weiss T, Herold-Mende C, Zhang F, Kockmann T, Sahm F, Aebersold R, von Deimling A, Reuss DE, Histone epiproteomic profiling distinguishes oligodendroglioma, IDH-mutant and 1p/19q co-deleted from IDH-mutant astrocytoma and reveals less tri-methylation of H3K27 in oligodendrogliomas. Acta Neuropathol, 139(1):211-213(2020) [pubmed] |
10.1007/s00401-019-02096-8; |
Keyword List
curator keyword: Biomedical |
submitter keyword: Oligodendroglioma,histone modifications, brain cancer, Astrocytoma, histone epi-proteome |
Contact List
Ruedi Aebersold |
contact affiliation | Department of Biology, Institute of Molecular Systems Biology, ETH Zürich, Otto Stern Weg 3, 8093, Zürich, Switzerland |
contact email | aebersold@imsb.biol.ethz.ch |
lab head | |
Christian Feller |
contact affiliation | ETH Zurich |
contact email | feller.christian@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD015151
- Label: PRIDE project
- Name: Histone Modification Analysis of Oligodendroglioma and Astrocytoma Brain Cancer Samples