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Exosomal and Non-Exosomal Urinary miRNAs in Prostate Cancer Detection and Prognosis.
Foj, Laura; Ferrer, Ferran; Serra, Marta; Arévalo, Antonio; Gavagnach, Montserrat; Giménez, Nuria; Filella, Xavier.
Afiliación
  • Foj L; Department of Biochemistry and Molecular Genetics (CDB), Hospital Clínic, IDIBAPS, Barcelona, Catalonia, Spain.
  • Ferrer F; Department of Radiotherapy, Institut Català d'Oncologia, IDIBELL, Department of Clinical Sciences-Bellvitge Health Sciences Campus, University of Barcelona, L'Hospitalet de Llobregat, Catalonia, Spain.
  • Serra M; CAP Valldoreix, Sant Cugat del Vallès, Catalonia, Spain.
  • Arévalo A; CAP Valldoreix, Sant Cugat del Vallès, Catalonia, Spain.
  • Gavagnach M; CAP Valldoreix, Sant Cugat del Vallès, Catalonia, Spain.
  • Giménez N; Research Unit, Fundació de Recerca Mútua Terrassa, Terrassa, Catalonia, Spain.
  • Filella X; Department of Biochemistry and Molecular Genetics (CDB), Hospital Clínic, IDIBAPS, Barcelona, Catalonia, Spain.
Prostate ; 77(6): 573-583, 2017 May.
Article en En | MEDLINE | ID: mdl-27990656
ABSTRACT

BACKGROUND:

MicroRNAs (miRNAs) are non-coding small RNAs, involved in post-transcriptional regulation of many target genes.

METHODS:

Five miRNAs that have been consistently found deregulated in PCa (miR-21, miR-141, miR-214, miR-375, and let-7c) were analyzed in urinary pellets from 60 prostate cancer (PCa) patients and 10 healthy subjects by qRT-PCR. Besides, urinary exosomes were isolated by differential centrifugation and analyzed for those miRNAs.

RESULTS:

Significant upregulation of miR-21, miR-141, and miR-375 was found comparing PCa patients with healthy subjects in urinary pellets, while miR-214 was found significantly downregulated. Regarding urinary exosomes, miR-21 and miR-375 were also significantly upregulated in PCa but no differences were found for miR-141. Significant differences were found for let-7c in PCa in urinary exosomes while no differences were observed in urinary pellets. A panel combining miR-21 and miR-375 is suggested as the best combination to distinguish PCa patients and healthy subjects, with an AUC of 0.872. Furthermore, the association of miRNAs with clinicopathological characteristics was investigated. MiR-141 resulted significantly correlated with Gleason score in urinary pellets and let-7c with clinical stage in urinary exosomes. Additionally, miR-21, miR-141, and miR-214 were found significantly deregulated in intermediate/high-risk PCa versus low-risk/healthy subjects in urinary pellets. Significant differences between both groups were found in urinary exosomes for miR-21, miR-375, and let-7c.

CONCLUSIONS:

These findings suggest that the analysis of miRNAs-especially miRNA-21 and miR-375- in urine could be useful as biomarkers in PCa. Prostate 77 573-583, 2017. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Biomarcadores de Tumor / MicroARNs / Exosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Biomarcadores de Tumor / MicroARNs / Exosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article