PXD007982 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Quantitive protein profiling and pathway analysis for spinal arteriovenous malformations |
Description | Spinal arteriovenous malformations (sAVM) were rare and heterogeneous group of blood vessel disorders that affected the function of spinal cord directly or indirectly. In the past decades, the pathogenesis for SAVM was still not elucidated. Here we compared the specimens of four sAVM obtained from surgery and control samples from donations using TMT labeled proteomic study. In our proteomic study, we identified a total of 3101 proteins and 654-proteins were changed in SAVM compares with control, among which 96 proteins were upregulated and 358 proteins were downregulated. Gene Ontology (GO) analysis revealed that extracellular matrix organization in biological process and integrin binding proteins in molecular function were the most enriched items. Four significant changed proteins (PLG, MPZ, MMP9 and RPL23a) were verified by Western blot. The pathway analysis revealed that the changed proteins in pathways of angiogenesis, focal adhesion and cytoplasmic ribosome likely contributed to SAVM. The protein profile changes identified by our proteomic studies provide a comprehensive understanding of sAVM for us. |
HostingRepository | PRIDE |
AnnounceDate | 2018-06-18 |
AnnouncementXML | Submission_2018-06-18_01:51:48.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Wei Ge |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | TMT6plex-126 reporter+balance reagent acylated residue; iodoacetamide derivatized residue |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2017-10-17 07:26:27 | ID requested | |
⏵ 1 | 2018-06-18 01:51:49 | announced | |
Publication List
Guo Y, Xu B, Sun Z, Wu Y, Shi W, Wang J, Meng X, Ge W, Wang G, Quantitative protein profiling and pathway analysis of spinal arteriovenous malformations. Microvasc Res, 120():47-54(2018) [pubmed] |
Keyword List
curator keyword: Biomedical |
submitter keyword: Spinal arteriovenous malformation, Proteomic, Angiogenesis, Focal adhesion, Ribosome |
Contact List
Wei Ge |
contact affiliation | State Key Laboratory of Medical Molecular Biology & Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, No. 5 Dongdansantiao, Dongcheng District, Beijing, 100005 China |
contact email | wei.ge@chem.ox.ac.uk |
lab head | |
Wei Ge |
contact affiliation | National Key Laboratory of Medical Molecular Biology & Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences |
contact email | wei.ge@chem.ox.ac.uk |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/06/PXD007982 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD007982
- Label: PRIDE project
- Name: Quantitive protein profiling and pathway analysis for spinal arteriovenous malformations