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Abstract
Experimental design: To investigate this, we compared the proteome composition of the renal pelvis urine (RPU) and individually self-voided bladder urine (BU) collected from seven unilateral urinary tract obstruction male patients by LC-MS/MS screening. To our knowledge, this is the first proteomic comparison of RPU and BU samples from the same individual.
Results: Overall, RPU and BU proteomes did not exhibit proteins that were exclusively present in all samples of one urine type while in none of the other type. Nonetheless, BU had more overrepresented proteins that were observed at a higher frequency than RPU. Label-free quantitative analyses revealed BU–RPU differential proteins that are enriched in exosomes and extracellular proteins. However, the differences were not significant after corrections for multiple testing. Interestingly, we observed a significant increase of collagen peptides with hydroxyproline modifications in the BU samples, suggesting differences in protein modifications.
Conclusions and clinical relevance: Our study revealed no substantial differences at the protein level between the BU and RPU samples. Future investigations with expanded cohorts would provide more insights about the urothelial–urinary interactions.
©2023 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | 2300004 |
| Journal | Proteomics - Clinical Applications |
| Volume | 18 |
| Issue number | 2 |
| Online published | 13 Aug 2023 |
| DOIs | |
| Publication status | Published - Mar 2024 |
Funding
This work was supported by grants from the Shenzhen Science and Technology Innovation Commission (JCYJ20210324133812034), Hetao Shenzhen‐Hong Kong Science and Technology Innovation Cooperation Zone Shenzhen Park Project (HZQB‐KCZYZ‐2021017), the Research Grants Council of Hong Kong (11104423 and R1020‐18), and a grant from the Tung Foundation Biomedical Sciences Centre (9609301).
RGC Funding Information
- RGC-funded
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ASDC_Sub: Screen for Molecular Targets in the Senescence Response of Tumor Cells to Chemotherapy
ZHANG, L. (Principal Investigator / Project Coordinator)
1/02/21 → 15/04/24
Project: Research