PXD046096 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Multi-omics analysis of the bladder and its sensitivity to inosine in a rat model of spinal cord injury |
Description | This study investigates the molecular changes in the bladder following spinal cord injury (SCI) in rats and the impact of inosine treatment using a multi-omics approach. We discovered the activation of PARP (Poly(ADP-ribose) polymerase) in response to SCI, a previously unrecognized phenomenon, and its attenuation with inosine treatment. SCI triggered significant DNA damage and oxidative stress pathways, whereas inosine treatment prevents DNA damage and inhibits PARP activation, offering a potential therapeutic avenue. The integrated analysis of transcriptomics and proteomics data revealed concordant regulation of multiple pathways following SCI, including EIF2 signaling and NRF2-mediated oxidative stress response, which are ameliorated by inosine treatment. These findings have relevance to human neurogenic bladder pathobiology. Pathway inhibition by inosine in the setting of SCI suggests its potential for neuroprotection in the bladder. Despite limitations, such as the focus on male rats and a lack of proteomics data from separated detrusor and mucosa, this study provides valuable insights into the molecular mechanisms underlying bladder dysfunction following SCI. It also suggests the repurposing of FDA-approved PARP inhibitors for the treatment of bladder dysfunction following spinal injury. |
HostingRepository | PRIDE |
AnnounceDate | 2025-07-14 |
AnnouncementXML | Submission_2025-07-13_16:09:50.435.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Wei Yang |
SpeciesList | scientific name: Rattus norvegicus (Rat); NCBI TaxID: 10116; |
ModificationList | acetylated residue; monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-10-12 13:39:59 | ID requested | |
⏵ 1 | 2025-07-13 16:09:51 | announced | |
Publication List
10.1172/jci.insight.180275; |
Hashemi Gheinani A, Sack BS, Bigger-Allen A, Thaker H, Atta H, Lambrinos G, Costa K, Doyle C, Gharaee-Kermani M, Patalano S, Piper M, Cotellessa JF, Vitko D, Li H, Kadayil Prabhakaran M, Cristofaro V, Froehlich J, Lee RS, Yang W, Sullivan MP, Macoska JA, Adam RM, Multiomics analysis unveils an inosine-sensitive DNA damage response in neurogenic bladder after spinal cord injury. JCI Insight, 10(12):(2025) [pubmed] |
Keyword List
submitter keyword: Multi-Omics, Spinal Cord Injury, Inosine, Bladder, Rat |
Contact List
Wei Yang |
contact affiliation | Department of Pathology Cancer Center Stony Brook University |
contact email | wei.yang@stonybrook.edu |
lab head | |
Wei Yang |
contact affiliation | Stony Brook University |
contact email | omician@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD046096
- Label: PRIDE project
- Name: Multi-omics analysis of the bladder and its sensitivity to inosine in a rat model of spinal cord injury