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

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          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.

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          Most cited references31

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          High-throughput microRNAome analysis in human germ cell tumours.

          Testicular germ cell tumours (GCTs) of adolescents and adults can be subdivided into seminomas (referred to as dysgerminomas of the ovary) and non-seminomas, all referred to as type II GCTs. They originate from carcinoma in situ (CIS), being the malignant counterparts of primordial germ cells (PGCs)/gonocytes. The invasive components mimic embryogenesis, including the stem cell component embryonal carcinoma (EC), the somatic lineage teratoma (TE), and the extra-embryonic tissues yolk sac tumour (YST) and choriocarcinoma (CH). The other type is the so-called spermatocytic seminomas (SS, type III GCT), composed of neoplastic primary spermatocytes. We reported previously that the miRNAs hsa-miR 371-373 cluster is involved in overruling cellular senescence induced by oncogenic stress, allowing cells to become malignant. Here we report the first high-throughput screen of 156 microRNAs in a series of type II and III GCTs (n = 69, in duplicate) using a quantitative PCR-based approach. After normalization to allow inter-sample analysis, the technical replicates clustered together, and the previous hsa-miRNA 371-373 cluster finding was confirmed. Unsupervised cluster analysis demonstrated that the cell lines are different from the in vivo samples. The in vivo samples, both normal and malignant, clustered predominantly based on their maturation status. This parallels normal embryogenesis, rather than chromosomal anomalies in the tumours. miRNAs within a single cluster showed a similar expression pattern, implying common regulatory mechanisms. Normal testicular tissue expressed most discriminating miRNAs at a higher level than SE and SS. Moreover, differentiated non-seminomas showed overexpression of discriminating miRNAs. These results support the model that miRNAs are involved in regulating differentiation of stem cells, retained in GCTs. Copyright 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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            Circulating serum miRNA (miR-367-3p, miR-371a-3p, miR-372-3p and miR-373-3p) as biomarkers in patients with testicular germ cell cancer.

            Classic serum tumor markers (human chorionic gonadotropin, α1-fetoprotein and lactate dehydrogenase) have an important role in managing testicular germ cell tumor. Since only 60% of all patients with testicular germ cell tumor have elevations of these markers, there is a need for new biomarkers with greater sensitivity/specificity. miRNAs are deregulated in cancer and could serve as noninvasive serum biomarkers. We explored the role of serum miRNAs as a novel biomarker in patients with testicular germ cell tumor.
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              Serum Levels of MicroRNA miR-371a-3p: A Sensitive and Specific New Biomarker for Germ Cell Tumours.

              Clinical management of germ cell tumours (GCTs) relies on monitoring of serum tumour markers. However, the markers α-fetoprotein (AFP), the β-subunit of human chorionic gonadotropin (bHCG), and lactate dehydrogenase (LDH) are expressed in <60% of GCT cases.
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                Author and article information

                Contributors
                +49421 21899646 , aradtke@uni-bremen.de
                Journal
                J Cancer Res Clin Oncol
                J. Cancer Res. Clin. Oncol
                Journal of Cancer Research and Clinical Oncology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0171-5216
                1432-1335
                17 August 2017
                17 August 2017
                2017
                : 143
                : 11
                : 2383-2392
                Affiliations
                [1 ]ISNI 0000 0001 2297 4381, GRID grid.7704.4, Faculty of Biology and Chemistry, , University of Bremen, ; Leobener Str. 2, 28359 Bremen, Germany
                [2 ]ISNI 0000 0001 2172 9288, GRID grid.5949.1, Department of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, , University of Muenster, ; Muenster, Germany
                [3 ]ISNI 0000 0004 0636 7065, GRID grid.419807.3, Department of Pathology, , Klinikum Bremen-Mitte, ; Bremen, Germany
                [4 ]ISNI 0000 0001 0057 2672, GRID grid.4562.5, Department of Cardiac and Thoracic Vascular Surgery, , University of Luebeck, ; Luebeck, Germany
                [5 ]Department of Urology, Albertinen Krankenhaus, Hamburg, Germany
                Author information
                http://orcid.org/0000-0002-2439-9699
                Article
                2490
                10.1007/s00432-017-2490-7
                5640733
                28819887
                aed8ddb5-0502-4cde-bd62-5b17c6828c4e
                © 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.

                History
                : 17 May 2017
                : 1 August 2017
                Funding
                Funded by: Rotary Club Hamburg Blankenese
                Award ID: 2017/2602
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100008672, Wilhelm Sander-Stiftung;
                Award ID: 2014.178.1
                Award Recipient :
                Categories
                Original Article – Clinical Oncology
                Custom metadata
                © Springer-Verlag GmbH Germany 2017

                Oncology & Radiotherapy
                germ cell tumour,microrna,germ cell neoplasia in situ,testicular biopsy,quantitative polymerase chain reaction

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