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PXD079732
PXD079732 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | STAT3/POSTN/GSTP1/JNK Axis Orchestrates Ferroptosis in Nucleus Pulposus Cells:A Potential Therapeutic Target for Intervertebral Disc Degeneration |
| Description | Objective: This study aimed to investigate the role of the STAT3/POSTN/GSTP1/JNK axis in ferroptosis and extracellular matrix (ECM) metabolic imbalance in nucleus pulposus cells (NPCs) during intervertebral disc degeneration (IDD) and to explore therapeutic strategies targeting this axis. Methods: Using integrated multi-omics sequencing, transcriptional regulation assays (ChIP, dual‑luciferase reporter), protein interaction analysis (Co‑IP), and other molecular biology approaches, we systematically elucidated that the regulatory role of the STAT3/POSTN/GSTP1/JNK axis in ferroptosis of NPCs during IDD. Functional validation was performed in POSTN‑edited cell and rat models as well as in a needle‑puncture‑induced rat IDD model. A small‑molecule candidate targeting this axis was identified through virtual screening, molecular docking, and molecular dynamics simulations. Results: POSTN expression increased during ferroptosis and induced ferroptosis and ECM metabolic imbalance in NPCs in a concentration- and time-dependent manner. STAT3 was identified as a transcriptional regulator of POSTN and interacted with POSTN to form a self-amplifying positive feedback loop, accelerating ferroptosis progression. Furthermore, POSTN impaired the binding of the GSTP1/JNK complex, leading to the depletion of cellular GSH. Chemical screening identified Pristimerin (PN) as a direct activator of GSTP1, targeting the STAT3/POSTN/GSTP1/JNK axis and delaying IDD progression. Conclusion: This study revealed the important role of the STAT3/POSTN/GSTP1/JNK axis in regulating ferroptosis and ECM metabolism in NPCs and highlighted PN as a promising candidate therapeutic agent for IDD. These findings provide new insights into the molecular mechanisms underlying IDD and offer new targeted therapeutic avenues for IDD. |
| HostingRepository | iProX |
| AnnounceDate | 2026-06-14 |
| AnnouncementXML | Submission_2026-06-15_17:42:46.357.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Zhaoheng Wang |
| SpeciesList | scientific name: Rattus norvegicus; NCBI TaxID: 10116; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | Orbitrap Astral |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2026-06-15 17:42:24 | ID requested | |
| ⏵ 1 | 2026-06-15 17:42:46 | announced |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: Intervertebral disc degeneration, Nucleus pulposus cells, Periostin, Ferroptosis, STAT3, GSTP1 |
Contact List
| Xuewen Kang | |
|---|---|
| contact affiliation | Lanzhou University Second Hospital |
| contact email | ery_kangxw@lzu.edu.cn |
| lab head | |
| Zhaoheng Wang | |
| contact affiliation | Lanzhou University Second Hospital |
| contact email | wangzhh2023@lzu.edu.cn |
| dataset submitter | |
Full Dataset Link List
| iProX dataset URI |




