Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?

Radtke A., Cremers J., Kliesch S., Riek S., Junker K., Mohamed S., Anheuser P., Belge G., Dieckmann K.

Research article (journal) | Peer reviewed

Abstract

Purpose: Diagnosing germ cell neoplasia in situ (GCNis) can detect germ cell tumours (GCTs) at the pre-invasive stage. To date, testicular biopsy with the potential of surgical complications is the only way of safely diagnosing GCNis. Recently, microRNAs (miRs) 371-3, and miR 367 were shown to be valuable serum biomarkers of GCTs. We explored the usefulness of these candidate miRs as a marker for GCNis. Methods: 27 patients with GCNis and no concomitant GCT were enrolled. All patients underwent measuring serum levels of miR-371a-3p and miR-367-3p before treatment, 11 had repeat measurement after treatment, 2 also had testicular vein blood examinations. Serum levels were measured by quantitative PCR. In addition, four orchiectomy specimens of patients with GCT were examined immunohistochemically and by in situ hybridization (ISH) with a probe specific for miR-371a-3p to look for the presence of this miR in GCNis cells. Results: The median serum level of miR-371a-3p was significantly higher in patients with GCNis than in controls, miR-367 levels were not elevated. Overall, 14 patients (51.9%) had elevated serum levels of miR-371a-3p. The highest levels were found in patients with bilateral GCNis. Levels in testicular vein serum were elevated in both of the cases. After treatment, all elevated levels dropped to normal. In two orchiectomy specimens, miR-371a-3p was detected by ISH in GCNis cells. Conclusions: Measuring miR-371a-3p serum levels can replace control biopsies after treatment of GCNis. In addition, the test can guide clinical decision making regarding the need of testicular biopsy in cases suspicious of GCNis.

Details about the publication

JournalJournal of Cancer Research and Clinical Oncology
Volume143
Issue11
Page range2383-2392
StatusPublished
Release year2017
Language in which the publication is writtenEnglish
DOI10.1007/s00432-017-2490-7
Link to the full texthttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027887671&origin=inward
KeywordsGerm cell neoplasia in situ; Germ cell tumour; microRNA; Quantitative polymerase chain reaction; Testicular biopsy

Authors from the University of Münster

Cremers, Jann-Frederik
Abteilung für Klinische Andrologie
Kliesch, Sabine
Abteilung für Klinische Andrologie