PXD050476-1
PXD050476 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | USP9X coordinates TGF-β and hypoxia signalings to promote ovarian cancer chemoresistance via maintaining cancer stem cells |
| Description | Widespread intraperitoneal metastases and chemoresistance has made ovarian cancer the leading cause of gynecological malignancy–related deaths, wherein TGF-β signaling plays the pivotal role by promoting cancer stem cells (CSCs) activity. Whereas, how the signaling is activated and how to target TGF-β signaling precisely remain as key challenges. Here, we identify hypoxic tumor microenvironment as the initiator of TGF-β signaling so as to induce HIF-2α positive CSCs and chemoresistance in HGSOC. Mechanistically, deubiquitinase USP9X, as the TGF-β downstream effector, stabilizes HIF-2ɑ in hydroxylation and ubiquitylation dependent manner, thus activates stemness programming. Hypoxia and TGF-β signals promote USP9X-HIF-2ɑ axis via multi-level regulations, which in turn facilitates Smad/HIF responses, thus coordinating the two pathways. Clinical USP9X is highly correlated with TGF-β signatures, CSCs characteristics, EMT behaviors, and stimulated by chemotherapies, along with HIF-2ɑ. Antagonizing USP9X efficiently represses tumor formation, metastasis, CSCs occurrence, while increases chemosensitivity, through orthotopic tumor, patient derived xenograft (PDX), organoid and chemoresistant cell models, via restricting TGF-β and hypoxia activities. This study deciphers the critical role of hypoxic niche in turning up TGF-β signaling, as well as USP9X-HIF-2ɑ proteostatic regulation in priming the HGSOC stemness, thus provides a promising strategy to counteract TGF-β signaling by targeting USP9X in CSCs and meliorate clinical chemoresistance. |
| HostingRepository | iProX |
| AnnounceDate | 2024-03-08 |
| AnnouncementXML | Submission_2025-08-28_23:57:23.603.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Zhenlei Zhang |
| SpeciesList | scientific name: Homo sapiens; NCBI TaxID: 9606; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | Q Exactive Plus |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2024-03-08 01:47:30 | ID requested | |
| ⏵ 1 | 2025-08-28 23:57:25 | announced |
Publication List
| Zhang Z, Yu X, Wen L, Wang J, Li Z, Zhang Y, Cheng J, Kan R, Zhang W, Shen Y, Yuan S, Zhao L, -maintained stemness. Cell Death Dis, 16(1):312(2025) [pubmed] |
Keyword List
| submitter keyword: AP-MS, USP9X, HIF-2α |
Contact List
| Li Zhao | |
|---|---|
| contact affiliation | Tianjin Medical University |
| contact email | shzhaoli@tmu.edu.cn |
| lab head | |
| Zhenlei Zhang | |
| contact affiliation | Tianjin Medical University |
| contact email | zhangzhenlei0413@tmu.edu.cn |
| dataset submitter | |
Full Dataset Link List
| iProX dataset URI |




