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

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 va...

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Autores principales: Radtke, A., Cremers, J.-F., Kliesch, S., Riek, S., Junker, K., Mohamed, S. A., Anheuser, P., Belge, G., Dieckmann, K.-P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640733/
https://www.ncbi.nlm.nih.gov/pubmed/28819887
http://dx.doi.org/10.1007/s00432-017-2490-7
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author Radtke, A.
Cremers, J.-F.
Kliesch, S.
Riek, S.
Junker, K.
Mohamed, S. A.
Anheuser, P.
Belge, G.
Dieckmann, K.-P.
author_facet Radtke, A.
Cremers, J.-F.
Kliesch, S.
Riek, S.
Junker, K.
Mohamed, S. A.
Anheuser, P.
Belge, G.
Dieckmann, K.-P.
author_sort Radtke, A.
collection PubMed
description 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.
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spelling pubmed-56407332017-10-26 Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p? Radtke, A. Cremers, J.-F. Kliesch, S. Riek, S. Junker, K. Mohamed, S. A. Anheuser, P. Belge, G. Dieckmann, K.-P. J Cancer Res Clin Oncol Original Article – Clinical Oncology 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. Springer Berlin Heidelberg 2017-08-17 2017 /pmc/articles/PMC5640733/ /pubmed/28819887 http://dx.doi.org/10.1007/s00432-017-2490-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article – Clinical Oncology
Radtke, A.
Cremers, J.-F.
Kliesch, S.
Riek, S.
Junker, K.
Mohamed, S. A.
Anheuser, P.
Belge, G.
Dieckmann, K.-P.
Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title_full Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title_fullStr Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title_full_unstemmed Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title_short Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?
title_sort can germ cell neoplasia in situ be diagnosed by measuring serum levels of microrna371a-3p?
topic Original Article – Clinical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640733/
https://www.ncbi.nlm.nih.gov/pubmed/28819887
http://dx.doi.org/10.1007/s00432-017-2490-7
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