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PXD071235-1
PXD071235 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Discovery and validation of lung cancer biomarkers based on proteomic analysis of bronchoalveolar lavage fluid from the self-controlled pulmonary lobe |
| Description | Background: Distinguishing indeterminate pulmonary nodules remains a significant challenge in the early diagnosis of lung cancer, while proteomic biomarkers derived from the lesioned pulmonary lobe may provide crucial insights into their malignant progression. Methods: Our study cohort included three groups: the lesioned lobe of lung cancer patients (LC-L), the paired non-lesioned lobe of lung cancer patients (LC-N), and the lesioned lobe of patients with benign nodules (BN-L). Data-independent acquisition (DIA) proteomic analysis was performed to identify potential biomarkers for early diagnosis of lung cancer, followed by evaluation in a larger, independent cohort. Results: We identified 4,305 proteins, among which 715 and 738 were differentially expressed between LC-L and LC-N, and between LC-L and BN-L, respectively. Integration of these results revealed 134 up-regulated and 44 down-regulated proteins (p < 0.05; |FC| > 1.2). Notably, 14 proteins exhibited a |FC| > 3, and 5 of them were either involved in biological metabolism or had been previously reported as cancer-associated. KEGG pathway enrichment analysis of the 134 up-regulated proteins demonstrated significant enrichment in metabolic pathways and the TCA cycle. We further validated 9 candidate proteins by ELISA and confirmed that 3 proteins (SUCLA2, FKBP9, TAP1) exhibited expression patterns consistent with those observed in the discovery cohort. Among them, SUCLA2 and FKBP9 reached statistical significance, while TAP1 showed a strong trend (p = 0.061). To our knowledge, this is the first report showing that SUCLA2 and FKBP9 are up-regulated in the lesioned lobes of lung cancer patients, independent of benign nodules. Conclusions: These candidate biomarkers and their associated metabolic reprogramming pathways provide a new direction for improving the identification ability of uncertain nodules, and expand our understanding of the pathophysiology of early lung cancer. |
| HostingRepository | iProX |
| AnnounceDate | 2025-11-25 |
| AnnouncementXML | Submission_2025-11-25_18:03:41.677.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Shihui Wei |
| SpeciesList | scientific name: Homo sapiens; NCBI TaxID: 9606; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | timsTOF Pro |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2025-11-25 18:03:21 | ID requested | |
| ⏵ 1 | 2025-11-25 18:03:42 | announced |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: lung cancer, BALF, DIA, proteomic, SUCLA2, FKBP9, TAP1 |
Contact List
| Chao Cao | |
|---|---|
| contact affiliation | The First Affiliated Hospital of Ningbo University |
| contact email | caocdoctor@163.com |
| lab head | |
| Shihui Wei | |
| contact affiliation | The First Affiliated Hospital of Ningbo University |
| contact email | 19032170599@163.com |
| dataset submitter | |
Full Dataset Link List
| iProX dataset URI |




