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Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer

Circulating nucleic acids are found in free form in body fluids and may serve as minimally invasive tools for cancer diagnosis and prognosis. Only a few studies have investigated the potential application of circulating mRNAs and microRNAs (miRNAs) in prostate cancer (PCa). The Cancer Genome Atlas (...

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Autores principales: de Souza, Marilesia Ferreira, Kuasne, Hellen, Barros-Filho, Mateus de Camargo, Cilião, Heloísa Lizotti, Marchi, Fabio Albuquerque, Fuganti, Paulo Emilio, Paschoal, Alexandre Rossi, Rogatto, Silvia Regina, Cólus, Ilce Mara de Syllos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598937/
https://www.ncbi.nlm.nih.gov/pubmed/28910345
http://dx.doi.org/10.1371/journal.pone.0184094
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author de Souza, Marilesia Ferreira
Kuasne, Hellen
Barros-Filho, Mateus de Camargo
Cilião, Heloísa Lizotti
Marchi, Fabio Albuquerque
Fuganti, Paulo Emilio
Paschoal, Alexandre Rossi
Rogatto, Silvia Regina
Cólus, Ilce Mara de Syllos
author_facet de Souza, Marilesia Ferreira
Kuasne, Hellen
Barros-Filho, Mateus de Camargo
Cilião, Heloísa Lizotti
Marchi, Fabio Albuquerque
Fuganti, Paulo Emilio
Paschoal, Alexandre Rossi
Rogatto, Silvia Regina
Cólus, Ilce Mara de Syllos
author_sort de Souza, Marilesia Ferreira
collection PubMed
description Circulating nucleic acids are found in free form in body fluids and may serve as minimally invasive tools for cancer diagnosis and prognosis. Only a few studies have investigated the potential application of circulating mRNAs and microRNAs (miRNAs) in prostate cancer (PCa). The Cancer Genome Atlas (TCGA) database was used for an in silico analysis to identify circulating mRNA and miRNA as potential markers of PCa. A total of 2,267 genes and 49 miRNAs were differentially expressed between normal and tumor samples. The prediction analyses of target genes and integrative analysis of mRNA and miRNA expression revealed eleven genes and eight miRNAs which were validated by RT-qPCR in plasma samples from 102 untreated PCa patients and 50 cancer-free individuals. Two genes, OR51E2 and SIM2, and two miRNAs, miR-200c and miR-200b, showed significant association with PCa. Expression levels of these transcripts distinguished PCa patients from controls (67% sensitivity and 75% specificity). PCa patients and controls with prostate-specific antigen (PSA) ≤ 4.0 ng/mL were discriminated based on OR51E2 and SIM2 expression levels. The miR-200c expression showed association with Gleason score and miR-200b, with bone metastasis, bilateral tumor, and PSA > 10.0 ng/mL. The combination of circulating mRNA and miRNA was useful for the diagnosis and prognosis of PCa.
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spelling pubmed-55989372017-09-22 Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer de Souza, Marilesia Ferreira Kuasne, Hellen Barros-Filho, Mateus de Camargo Cilião, Heloísa Lizotti Marchi, Fabio Albuquerque Fuganti, Paulo Emilio Paschoal, Alexandre Rossi Rogatto, Silvia Regina Cólus, Ilce Mara de Syllos PLoS One Research Article Circulating nucleic acids are found in free form in body fluids and may serve as minimally invasive tools for cancer diagnosis and prognosis. Only a few studies have investigated the potential application of circulating mRNAs and microRNAs (miRNAs) in prostate cancer (PCa). The Cancer Genome Atlas (TCGA) database was used for an in silico analysis to identify circulating mRNA and miRNA as potential markers of PCa. A total of 2,267 genes and 49 miRNAs were differentially expressed between normal and tumor samples. The prediction analyses of target genes and integrative analysis of mRNA and miRNA expression revealed eleven genes and eight miRNAs which were validated by RT-qPCR in plasma samples from 102 untreated PCa patients and 50 cancer-free individuals. Two genes, OR51E2 and SIM2, and two miRNAs, miR-200c and miR-200b, showed significant association with PCa. Expression levels of these transcripts distinguished PCa patients from controls (67% sensitivity and 75% specificity). PCa patients and controls with prostate-specific antigen (PSA) ≤ 4.0 ng/mL were discriminated based on OR51E2 and SIM2 expression levels. The miR-200c expression showed association with Gleason score and miR-200b, with bone metastasis, bilateral tumor, and PSA > 10.0 ng/mL. The combination of circulating mRNA and miRNA was useful for the diagnosis and prognosis of PCa. Public Library of Science 2017-09-14 /pmc/articles/PMC5598937/ /pubmed/28910345 http://dx.doi.org/10.1371/journal.pone.0184094 Text en © 2017 Souza et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
de Souza, Marilesia Ferreira
Kuasne, Hellen
Barros-Filho, Mateus de Camargo
Cilião, Heloísa Lizotti
Marchi, Fabio Albuquerque
Fuganti, Paulo Emilio
Paschoal, Alexandre Rossi
Rogatto, Silvia Regina
Cólus, Ilce Mara de Syllos
Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title_full Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title_fullStr Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title_full_unstemmed Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title_short Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
title_sort circulating mrnas and mirnas as candidate markers for the diagnosis and prognosis of prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598937/
https://www.ncbi.nlm.nih.gov/pubmed/28910345
http://dx.doi.org/10.1371/journal.pone.0184094
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