<<< Full experiment listing

PXD037378

PXD037378 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleQuantification of membrane protein expression in G0 and G1 cell cycle phase samples in PC3 prostate cancer cells
DescriptionProstate cancer (PCa) has a significant ability to disseminate and survive in the bone marrow (BM). Once there, disseminated tumor cells (DTCs) may lie dormant for years, but often eventually reactivate proliferative pathways, thus largely contributing to bone metastasis, disease progression, and relapse. Unfortunately, quiescent PCa cells are difficult to identify and target with treatment, in part because formerly identified relevant markers are intracellular and regulated by protein stability. We sought to address this problem by identifying a G0 marker that is expressed on the cell surface and therefore amenable to antibody binding for identification and therapeutic targeting. In doing so, we utilized stably transduced fluorescent markers for CDKN1B (p27) and CDT1 protein levels, which separate viable PCa cells into G0, G1, or combined S/G2/M populations (as described in PMID 34957090). We then performed FACS to collect G1 and G0 PC3 PCa cells, isolated membrane proteins, and subsequently used GC-MS proteomics to determine differences in protein abundance between G0 and G1. In total, 3,791 proteins were identified.
HostingRepositoryPRIDE
AnnounceDate2023-11-14
AnnouncementXMLSubmission_2023-11-14_08:24:52.072.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD037378
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterHenriette Remmer
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListacetylated residue; monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02022-10-13 14:48:36ID requested
12023-03-03 07:22:05announced
22023-11-14 08:24:53announced2023-11-14: Updated project metadata.
Publication List
10.6019/PXD037378;
Yumoto K, Rashid J, Ibrahim KG, Zielske SP, Wang Y, Omi M, Decker AM, Jung Y, Sun D, Remmer HA, Mishina Y, Buttitta LA, Taichman RS, Cackowski FC, HER2 as a potential therapeutic target on quiescent prostate cancer cells. Transl Oncol, 31():101642(2023) [pubmed]
Keyword List
submitter keyword: Dormancy, Disseminated Tumor Cells, Quiescent, ERBB2, HER2, G0, Cell Cycle, G1, Prostate Cancer
Contact List
Henriette Remmer
contact affiliationHenriette A. Remmer, Ph.D. Director, Proteomics & Peptide Synthesis Core University of Michigan C570C MSRB II SPC 5674 1150 W. Medical Center Drive Ann Arbor, MI 48109 https://brcf.medicine.umich.edu/cores/proteomics-peptide-synthesis/
contact emailHRemmer@umich.edu
lab head
Henriette Remmer
contact affiliationUniversity of Michigan
contact emailhremmer@umich.edu
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/2023/03/PXD037378
PRIDE project URI
Repository Record List
[ + ]