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tRNA-Derived Fragments as Biomarkers in Bladder Cancer
Olaf Strømme1, Kathleen A Heck1, Gaute Brede1
1Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, 7034 Trondheim, Norway.
Cancers
|April 27, 2024
Summary
Researchers identified transfer RNA-derived fragments (tRFs) in extracellular vesicles (EVs) as potential noninvasive biomarkers for bladder cancer (BC) diagnosis and monitoring recurrence-free survival.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Bladder cancer (BC) diagnosis relies on invasive cystoscopy, prompting the search for noninvasive biomarkers.
- Extracellular vesicles (EVs) in body fluids like urine and blood contain valuable molecular cargo, including RNA.
- Transfer RNA-derived fragments (tRFs) are a class of small noncoding RNAs found within EVs.
Purpose of the Study:
- To investigate the potential of tRFs within EVs as noninvasive biomarkers for bladder cancer.
- To compare tRF expression profiles in patients with non-muscle invasive BC versus non-cancer patients (NCPs).
- To assess tRFs for their utility in diagnosing BC and predicting recurrence-free survival.
Main Methods:
- Small-RNA next-generation sequencing was performed on urinary and serum EVs from 41 BC patients and 15 NCPs.
- Samples were collected pre- and post-surgery (transurethral resection of bladder tumors).
- Differential expression analysis identified specific tRFs (DEtRFs) and their genomic alignment was investigated.
Main Results:
- 14 differentially expressed tRFs (DEtRFs) were identified in urine EVs comparing T1 stage BC patients to NCPs.
- Six DEtRFs were found in serum supernatant comparing pre- and post-surgery samples in T1 stage patients.
- Four DEtRFs were identified in serum supernatant comparing pre-surgery samples to NCPs.
Conclusions:
- Specific tRFs in urine and serum EVs show potential as noninvasive biomarkers for bladder cancer diagnosis.
- These tRFs may aid in monitoring disease recurrence and predicting recurrence-free survival.
- The identified DEtRFs align with genomic regions involved in cancer development, suggesting functional relevance.
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