PXD044149 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Highly-reproducible quantitative proteomics analysis of pancreatic cancer cells reveals proteome-level effects of a novel combination drug therapy that induces cancer cell death via metabolic remodeling and activation of the extrinsic apoptosis pathway |
Description | A comprehensive in-vitro investigation of a novel chemotherapy drug combination. In this study, we employed a well-controlled quantitative proteomics pipeline to examine the temporal molecular interactions between gemcitabine (Gem) and BGJ398 (infigratinib), a recently-approved pan-FGFR inhibitor, in a pancreatic ductal adenocarcinoma (PDAC) cell line. |
HostingRepository | PRIDE |
AnnounceDate | 2024-11-19 |
AnnouncementXML | Submission_2024-11-19_03:01:55.579.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD044149 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Sailee Rasam |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-07-27 10:44:14 | ID requested | |
⏵ 1 | 2024-11-19 03:01:55 | announced | |
Publication List
Keyword List
submitter keyword: PDAC, Gemcitabine, BGJ398 |
Contact List
Dr. Jun Qu |
contact affiliation | University at Buffalo |
contact email | junqu@buffalo.edu |
lab head | |
Sailee Rasam |
contact affiliation | University at Buffalo |
contact email | saileesu@buffalo.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD044149
- Label: PRIDE project
- Name: Highly-reproducible quantitative proteomics analysis of pancreatic cancer cells reveals proteome-level effects of a novel combination drug therapy that induces cancer cell death via metabolic remodeling and activation of the extrinsic apoptosis pathway