PXD061033 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Deciphering the impact of ectopic SNAI1 expression on renal tubular cell proteome and functions |
| Description | Snail1 is crucial in regulating epithelial mesenchymal transition (EMT), which leads to excessive extracellular matrix (ECM) production and organ fibrosis including the kidney. Elucidating the roles of snail1 in EMT and kidney fibrosis is thus vital for developing targeted therapies. This study investigated the alterations in the proteome of SNAI1-overexpressed proximal tubular epithelial cells over the vector-transfected cells by label-free quantitative proteomics. Of 670 identified proteins, 233 showed significant changes due to ectopic snail1 expression. Of these, immunoblotting confirmed the decreased HSP60 and HSP70 while increased DDX1. X2K Appyter predicted the top ten transcription factors as key upstream regulators of the altered proteome. KEGG enrichment analysis revealed that these altered proteins were primarily associated with translational regulation, ribosome, cell cycle regulation, and cellular senescence. GO enrichment showed that focal adhesion, the structure where cells maintain cell interior-ECM interactions, was markedly overrepresented. Accordingly, functional validations demonstrated that SNAI1-overexpressed cells displayed aberrant ribosome biogenesis, indicated by increasing nucleophosmin and the nucleolar organizer regions. SNAI1-overexpressed cells exhibited senescent phenotypes including cell enlargement and increased granularity, up-regulated senescent makers p21 and γH2AX, and enhanced MMP-9 secretion. Moreover, SNAI1-overexpressed cells up-regulated paxillin, a scaffold protein located at focal adhesions crucial for their dynamic regulation. These findings provide insights into the molecular processes governed by snail1 during renal tubular cells undergoing EMT. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-04-27 |
| AnnouncementXML | Submission_2026-04-26_16:19:39.665.xml |
| DigitalObjectIdentifier | https://doi.org/10.6019/PXD061033 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Visith Thongboonkerd |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | LTQ Orbitrap XL |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-02-20 20:22:53 | ID requested | |
| ⏵ 1 | 2026-04-26 16:19:40 | announced | |
Publication List
| 10.1016/j.gendis.2025.101926; |
| Kanlaya R, Nonthawong K, Suntivichaya M, Yoodee S, Thongboonkerd V, gene on renal tubular cell proteome, nucleolar stress, ribosome biogenesis, senescence, DNA damage response, and focal adhesion dynamics. Genes Dis, 13(4):101926(2026) [pubmed] |
| 10.6019/PXD061033; |
Keyword List
| submitter keyword: Renal fibrosis, Senescence, Proteomics, Snail1,Kidney |
Contact List
| Prof. Visith Thongboonkerd |
| contact affiliation | Medical Proteomics Unit, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand |
| contact email | vthongbo@yahoo.com |
| lab head | |
| Visith Thongboonkerd |
| contact affiliation | Mahidol University |
| contact email | sirirajms@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD061033
- Label: PRIDE project
- Name: Deciphering the impact of ectopic SNAI1 expression on renal tubular cell proteome and functions