PXD034267-2
PXD034267 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Data-Independent Acquisition Proteomics Reveals Circulating Biomarkers of Coronary Chronic Total Occlusion in Humans |
| Description | The pathophysiology of chronic coronary total occlusion (CTO) has not been fully elucidated. In the present study, we aimed to investigate the potential plasma biomarkers associated with the pathophysiologic progression of CTO and identify protein dynamics in the plasma of CTO vessels immediately after successful revascularization. We quantitatively analyzed the plasma proteome profiles of controls (CON, n=10) and patients with CTO pre- and post- percutaneous coronary intervention (PCI) (CTO, n=10) by data-independent acquisition proteomics. A total of 1936 proteins with 69 differentially expressed proteins (DEPs) were detected in the plasma of patients with CTO through quantitative proteomics analysis. For all these DEPs, gene ontology (GO) analysis and protein-protein interaction (PPI) analysis were performed. The results showed that most of the proteins were related to the negative regulation of proteolysis, regulation of peptidase activity, negative regulation of hydrolase activity, humoral immune response, and lipid location. Furthermore, we identified 1927 proteins with 43 DEPs in the plasma of patients with CTO vessels after immediately successful revascularization compared to pre-PCI. GO analysis revealed that the above DEPs were enriched in the biological processes of extracellular structure organization, protein activation cascade, negative regulation of response to external stimulus, plasminogen activation, and fibrinolysis. More importantly, seven proteins, ADH4, CSF1, galectin, LPL, IGF2, IgH, and LGALS1, were found to be dynamically altered in plasma during the pathophysiological progression of CTO vessels and following successful revascularization. |
| HostingRepository | iProX |
| AnnounceDate | 2022-06-02 |
| AnnouncementXML | Submission_2023-01-28_18:21:23.877.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Qian Zhou |
| SpeciesList | scientific name: Homo sapiens; NCBI TaxID: 9606; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | Orbitrap Fusion |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2022-06-02 01:06:11 | ID requested | |
| 1 | 2022-12-04 16:26:53 | announced | |
| ⏵ 2 | 2023-01-28 18:21:24 | announced | 2023-01-29: Update publication information. |
Publication List
| Li J, Jiang XJ, Wang QH, Wu XL, Qu Z, Song T, Wan WG, Zheng XX, Yi X, Data-independent acquisition proteomics reveals circulating biomarkers of coronary chronic total occlusion in humans. Front Cardiovasc Med, 9():960105(2022) [pubmed] |
Keyword List
| submitter keyword: data-independent acquisition proteomics, coronary chronic total occlusion, protein dynamics, percutaneous coronary intervention, human |
Contact List
| Xin Yi | |
|---|---|
| contact affiliation | Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei, China |
| contact email | yixin321624@126.com |
| lab head | |
| Qian Zhou | |
| contact affiliation | Shanghai Omicsspace Biotech Co., Ltd. |
| contact email | zhouqian@omicsspace.com |
| dataset submitter | |
Full Dataset Link List
| iProX dataset URI |




