Evidence map›Paper›PMID 35171328›Full record

ArticleJournal of cancer research and clinical oncology2023

MicroRNA-profiling of miR-371~373- and miR-302/367-clusters in serum and cerebrospinal fluid identify patients with intracranial germ cell tumors.

Stefan Schönberger, Mahsa Mir Mohseni, Jörg Ellinger, Giao Vu Quynh Tran, Martina Becker, Alexander Claviez, Carl-Friedrich Classen, Barbara Hermes, Pablo Hernáiz Driever, Norbert Jorch and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 25 citations in OpenAlex.

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  11. Epigenetic Factors and ncRNAs in Testicular Cancer.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 12 institutions in 1 country.

Stefan Schönberger *Department of Pediatric Hematology and Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany. stefan.schoenberger@uk-essen.de.ORCID http://orcid.org/0000-0002-7222-296X
Mahsa Mir Mohseni *Department of Pediatric Hematology and Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.
Jörg EllingerDepartment of Urology and Center of Integrated Oncology (CIO), University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-7526-0857
Giao Vu Quynh TranDepartment of Pediatric Hematology and Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.
Martina BeckerDepartment of Pediatric Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.
Alexander ClaviezDepartment of Pediatrics, Pediatric Hematology and Oncology, Medical University of Schleswig-Holstein, Campus Kiel, Kiel, Germany.ORCID http://orcid.org/0000-0001-7064-8556
Carl-Friedrich ClassenUniversity Children's and Adolescents' Hospital, Rostock University Medical Center, Rostock, Germany.
Barbara HermesKreiskliniken Reutlingen, Medizinische Klinik I, Reutlingen, Germany.
Pablo Hernáiz DrieverDepartment of Pediatric Oncology and Hematology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany.
Norbert JorchDepartment of Pediatric Hematology and Oncology, Hospital of Bielefeld, Bielefeld, Germany.
Melchior LautenDepartment of Pediatric and Adolescent Medicine, Pediatric Hematology and Oncology, University Hospital Schleswig-Holstein, Lübeck, Germany.ORCID http://orcid.org/0000-0003-4774-0279
Marcus MehlitzDepartment of Neurosurgery, Krankenhaus der Barmherzigen Brüder Trier, Trier, Germany.
Niklas SchäferDivision of Clinical Neurooncology, Department of Neurology and Center of Integrated Oncology (CIO), University of Bonn, Bonn, Germany.
Johanna Scheer-PreissDepartment of Pediatric and Adolescent Medicine, Braunschweig Municipal Hospital, Brunswick, Germany.
Dominik T SchneiderClinic of Pediatrics, Dortmund Municipal Hospital, Dortmund, Germany.
Anja TroegerDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, University Hospital Regensburg, Regensburg, Germany.
Gabriele CalaminusDepartment of Pediatric Hematology and Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.
Dagmar DillooDepartment of Pediatric Hematology and Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.
University of Bonn · DEUniversity Hospital Schleswig-Holstein · DEGoethe University Frankfurt · DEHumboldt-Universität zu Berlin · DEKlinikum Bielefeld · DEKlinikum Braunschweig · DEKlinikum Dortmund · DEKrankenhaus der Barmherzigen Brüder Trier · DEKreiskliniken Reutlingen · DEUniversity Hospital Bonn · DEUniversity Hospital Regensburg · DEUniversity of Rostock · DE

Funding

Deutsche Kinderkrebsstiftung DKS2017.19
6 · The paper itself

Abstract

purposeIntracranial germ cell tumors (iGCT) comprise germinoma and non-germinoma. Their diagnosis predominantly relies on biopsy as only one-fifth of patients present with elevated biomarkers (AFP/ß-HCG) in serum or cerebrospinal fluid (CSF). MicroRNAs (miR/miRNA) have emerged as non-invasive biomarkers in extracranial GCT and may potentially facilitate non-invasive diagnosis in iGCT.

methodsWe analyzed eight miRNAs in serum and CSF from the miR-371~373- and miR-302/367-clusters and four miRNAs differentially expressed in iGCT tissue (miR-142-5p/miR-146a-5p/miR-335-5p/miR-654-3p) from eight iGCT patients (age 10-33 years) and 12 control subjects by pre-amplified RT-qPCR. MiR-30b-5p (serum) and miR-204-5p (CSF) acted as reference genes. ΔC

resultsBetween iGCT and control patients' serum ΔC

conclusionWith the largest data set so far, we underline the suitability of miR-371a, miR-372, miR-367 and miR-302d in serum and CSF for diagnosis of iGCT, particularly in biomarker-negative germinoma. Diagnosis of iGCT by miRNA analysis is a feasible and valid approach, particularly as serum can be readily obtained by a less invasive procedure. MiRNA analysis may discriminate iGCT from other tumors with similar radiological findings and may allow to monitor response to therapy as well as early relapse during follow-up.

Indexed as

GerminomaMicroRNAsAdolescentAdultBiomarkersBiomarkers, TumorChildHumansNeoplasm Recurrence, LocalYoung AdultBiomarkersBiomarkers, TumorMicroRNAsMIRN204 microRNA, humanMIRN371 microRNA, humanIntracranial germ cell tumorsLiquid biopsymiR-302dmiR-367miR-371miR-372

Identifiers

PMID35171328
PMCPMC9931786
OpenAlexW4226077524

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.