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MiR-30b-3p and miR-126-3p of urinary extracellular vesicles could be new biomarkers for prostate cancer

BACKGROUND: Extracellular vesicles (EVs) including exosomes are present in blood, urine, and saliva and contain proteins, microRNAs, and messenger RNAs. We investigated microRNAs in urinary EVs to discover new biomarkers of prostate cancer (PCa). METHODS: We isolated EVs from urine obtained followin...

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Detalles Bibliográficos
Autores principales: Matsuzaki, Kyosuke, Fujita, Kazutoshi, Tomiyama, Eisuke, Hatano, Koji, Hayashi, Yujiro, Wang, Cong, Ishizuya, Yu, Yamamoto, Yoshiyuki, Hayashi, Takuji, Kato, Taigo, Jingushi, Kentaro, Kawashima, Atsunari, Ujike, Takeshi, Nagahara, Akira, Uemura, Motohide, Tsujikawa, Kazutake, Nonomura, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100845/
https://www.ncbi.nlm.nih.gov/pubmed/33968679
http://dx.doi.org/10.21037/tau-20-421
Descripción
Sumario:BACKGROUND: Extracellular vesicles (EVs) including exosomes are present in blood, urine, and saliva and contain proteins, microRNAs, and messenger RNAs. We investigated microRNAs in urinary EVs to discover new biomarkers of prostate cancer (PCa). METHODS: We isolated EVs from urine obtained following digital rectal examination (DRE) of 14 men with elevated levels of serum prostate-specific antigen (PSA) [negative biopsy (n=4) and PCa with Gleason scores of 6 (n=3), 7 (n=3), and 8–9 (n=4)]. MicroRNAs extracted from EVs were analyzed by microRNA microarray. RESULTS: MicroRNAs miR-30b-3p and miR-126-3p were identified as being overexpressed in urinary EVs of the PCa patients versus the biopsy-negative men, but no microRNAs were associated with the Gleason score. In the independent cohort as well, these two microRNAs were overexpressed in urinary EVs from the PCa patients versus the negative-biopsy men. Logistic regression analysis adjusted by age and PSA showed that these two microRNAs were significantly associated with the prediction of PCa in biopsy specimens. Sensitivity and specificity of miR-30b-3p and miR-126-3p for the prediction of PCa were 46.4% and 88.0% and 60.7% and 80.0%, respectively, which were better than those of serum PSA (53.5% and 64.0%, respectively). CONCLUSIONS: MiR-30b-3p and miR-126-3p in urinary EVs could be potential biomarkers of PCa.