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

PLoS One. 2017 Sep 14;12(9):e0184094. doi: 10.1371/journal.pone.0184094. eCollection 2017.

Abstract

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.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Aged
  • Basic Helix-Loop-Helix Transcription Factors*
  • Biomarkers, Tumor / blood*
  • Bone Neoplasms / blood*
  • Bone Neoplasms / pathology
  • Bone Neoplasms / secondary
  • Bone Neoplasms / therapy
  • Humans
  • Kallikreins / blood
  • Male
  • MicroRNAs / blood*
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Proteins*
  • Prostate-Specific Antigen / blood
  • Prostatic Neoplasms / blood*
  • Prostatic Neoplasms / therapy
  • RNA, Messenger / blood*
  • RNA, Neoplasm / blood*
  • Receptors, Odorant*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers, Tumor
  • MIRN200 microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • OR51E2 protein, human
  • RNA, Messenger
  • RNA, Neoplasm
  • Receptors, Odorant
  • SIM2 protein, human
  • KLK3 protein, human
  • Kallikreins
  • Prostate-Specific Antigen

Grants and funding

This study was supported by grants from the Araucaria Foundation of Support for the Scientific and Technological of Paraná (185/2014), National Institute of Science and Technology in Oncogenomics (Sao Paulo Research Foundation FAPESP 2008/57887-9 and Brazilian National Council for Scientific and Technological Development CNPq 573589/08-9), Coordination for the Improvement of Higher Education Personnel Brazil (CAPES), Brazil and Vejle Hospital, Institute of Regional Health Research, Vejle, Denmark (K16-04V). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.