Articles producció científica> Medicina i Cirurgia

Liquid Biopsy-Based Exo-oncomiRNAs Can Predict Prostate Cancer Aggressiveness

  • Datos identificativos

    Identificador: imarina:9156319
    Handle: http://hdl.handle.net/20.500.11797/imarina9156319
  • Autores:

    Ruiz-Plazas, Xavier
    Altuna-Coy, Antonio
    Alves-Santiago, Marta
    Vila-Barja, Jose
    Garcia-Fontgivell, Joan Francesc
    Martinez-Gonzalez, Salome
    Segarra-Tomas, Jose
    Chacon, Matilde R.
  • Otros:

    Autor según el artículo: Ruiz-Plazas, Xavier; Altuna-Coy, Antonio; Alves-Santiago, Marta; Vila-Barja, Jose; Garcia-Fontgivell, Joan Francesc; Martinez-Gonzalez, Salome; Segarra-Tomas, Jose; Chacon, Matilde R.;
    Departamento: Ciències Mèdiques Bàsiques Medicina i Cirurgia
    Autor/es de la URV: Altuna Coy, Antonio / Alves Santiago, Marta / Martínez González, María Salomé / Rodríguez Chacón, Matilde / Segarra Tomas, Josep
    Palabras clave: Urinalysis Unclassified drug Tweak Tumor necrosis factor ligand superfamily member 12 Tumor microenvironment Transmission electron microscopy Transcription factor 12 Transcription factor Sensitivity and specificity Semen analysis Semen Rna isolation Rna analysis Real time polymerase chain reaction Protein serine threonine kinase Prostatectomy Prostate cancer Oncological parameters Nemo like kinase Microrna Male Major clinical study Low risk patient Liquid biopsy In vitro study Human cell Human High risk patient Gene targeting Gene expression regulation Gene expression Exosomes Exosome Exo-oncomirnas Exo oncomicrorna 423 5p Exo oncomicrorna 31 5p Exo oncomicrorna 222 3p Exo oncomicrorna 221 3p Exo oncomicrorna 193 3p Exo oncomicrorna Digital rectal examination Controlled study Cohort analysis Cancer prognosis Cancer growth Cancer aggressiveness Article Adult
    Resumen: Simple Summary The main problem encountered in the management of prostate cancer (PCa) is the inability to distinguish slow-growing indolent tumors from aggressive tumors. It is therefore important to explore non-invasive assays for the early detection of this aggressive subtype, when it can still be treated effectively. The presence of the TWEAK cytokine in biofluids of the PCa microenvironment might drive the secretion of extracellular vesicles (EVs) containing exo-oncomicroRNAs capable of modifying the tumor microenvironment. These exo-oncomicroRNAs are potentially useful as PCa biomarkers. We identified 2 exo-oncomiRNAs isolated from semen EVs by the action of TWEAK in the tumor microenvironment and, we determined their usefulness as biomarkers of PCa prognostic. We also established, for the first time, that TWEAK modulates potential exo-oncomiRNA targets, both tightly linked to cancer progression. In conclusion, our study shows that semen detection of TWEAK-regulated exo-oncomiRNAs can improve PCa prognosis, opening new avenues for diagnosis and treatment. Liquid biopsy-based biomarkers, including microRNAs packaged within extracellular vesicles, are promising tools for patient management. The cytokine tumor necrosis factor-like weak inducer of apoptosis (TWEAK) is related to PCa progression and is found in the semen of patients with PCa. TWEAK can induce the transfer of exo-oncomiRNAs from tumor cells to body fluids, and this process might have utility in non-invasive PCa prognosis. We investigated TWEAK-regulated exo-microRNAs in semen and in post-digital rectal examination urine from patients with different degrees of PCa aggressiveness. We first identified 14 exo-oncomiRNAs regulated by TWEAK in PCa cells in vitro, and subsequently validated those using liquid biopsies from 97 patients with PCa. Exo-oncomiR-221-3p, -222-3p and -31-5p were significantly higher in the semen of high-risk patients than in low-risk peers, whereas exo-oncomiR-193-3p and -423-5p were significantly lower in paired samples of post-digital rectal examination urine. A panel of semen biomarkers comprising exo-oncomiR-221-3p, -222-3p and TWEAK was designed that could correctly classify 87.5% of patients with aggressive PCa, with 85.7% specificity and 76.9% sensitivity with an area under the curve of 0.857. We additionally found that TWEAK modulated two exo-oncomiR-221-3p targets, TCF12 and NLK. Overall, we show that liquid biopsy detection of TWEAK-regulated exo-oncomiRNAs can improve PCa prognosis prediction.
    Áreas temáticas: Oncology Medicina iii Cancer research
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    Direcció de correo del autor: josep.segarra@urv.cat mariasalome.martinez@urv.cat matilde.rodriguez@urv.cat marta.alves@estudiants.urv.cat antonio.altuna@estudiants.urv.cat
    Identificador del autor: 0000-0001-6185-2889
    Fecha de alta del registro: 2023-03-11
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Enlace a la fuente original: https://www.mdpi.com/2072-6694/13/2/250
    URL Documento de licencia: http://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Cancers. 13 (2): 1-20
    Referencia de l'ítem segons les normes APA: Ruiz-Plazas, Xavier; Altuna-Coy, Antonio; Alves-Santiago, Marta; Vila-Barja, Jose; Garcia-Fontgivell, Joan Francesc; Martinez-Gonzalez, Salome; Segarr (2021). Liquid Biopsy-Based Exo-oncomiRNAs Can Predict Prostate Cancer Aggressiveness. Cancers, 13(2), 1-20. DOI: 10.3390/cancers13020250
    DOI del artículo: 10.3390/cancers13020250
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2021
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Cancer Research,Oncology
    Urinalysis
    Unclassified drug
    Tweak
    Tumor necrosis factor ligand superfamily member 12
    Tumor microenvironment
    Transmission electron microscopy
    Transcription factor 12
    Transcription factor
    Sensitivity and specificity
    Semen analysis
    Semen
    Rna isolation
    Rna analysis
    Real time polymerase chain reaction
    Protein serine threonine kinase
    Prostatectomy
    Prostate cancer
    Oncological parameters
    Nemo like kinase
    Microrna
    Male
    Major clinical study
    Low risk patient
    Liquid biopsy
    In vitro study
    Human cell
    Human
    High risk patient
    Gene targeting
    Gene expression regulation
    Gene expression
    Exosomes
    Exosome
    Exo-oncomirnas
    Exo oncomicrorna 423 5p
    Exo oncomicrorna 31 5p
    Exo oncomicrorna 222 3p
    Exo oncomicrorna 221 3p
    Exo oncomicrorna 193 3p
    Exo oncomicrorna
    Digital rectal examination
    Controlled study
    Cohort analysis
    Cancer prognosis
    Cancer growth
    Cancer aggressiveness
    Article
    Adult
    Oncology
    Medicina iii
    Cancer research
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