Evidence map›Paper›PMID 39888414›Full record

ArticleJournal of cancer research and clinical oncology2025

Biomarker microRNA-371a-3p - expression in malignancies other than germ-cell tumours.

Gazanfer Belge, Markus Klemke, Bendix Hansen, Cansu Dumlupinar, Aylin Igde, Dirk Arnold, Hans Salwender, Christian Wülfing, Armin Soave, Klaus-Peter Dieckmann

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Gazanfer BelgeDepartment of Tumour Genetics, Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany. belge@uni-bremen.de.
Markus KlemkeDepartment of Tumour Genetics, Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
Bendix HansenDepartment of Urology, Asklepios Tumorzentrum Hamburg, AK Altona, Hamburg, Germany.
Cansu DumlupinarDepartment of Tumour Genetics, Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
Aylin IgdeDepartment of Tumour Genetics, Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
Dirk ArnoldDepartment of Oncology, Asklepios Tumorzentrum Hamburg, AK Altona, Hamburg, Germany.
Hans SalwenderDepartment of Oncology, Asklepios Tumorzentrum Hamburg, AK Altona, Hamburg, Germany.
Christian WülfingDepartment of Urology, Asklepios Tumorzentrum Hamburg, AK Altona, Hamburg, Germany.
Armin Soave *Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Klaus-Peter Dieckmann *Department of Urology, Asklepios Tumorzentrum Hamburg, AK Altona, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposemicroRNA-371a-3p (M371) is considered a highly sensitive and specific serum biomarker of testicular germ cell tumours (GCTs). However, little is known about the expression of M371 in nontesticular malignancies (NTMs), so far. As knowledge about the expression of the marker in other malignancies is a prerequisite for the clinical application of the test we aimed to explore the M371 expression in other cancers.

methodsM371 serum levels were measured in 137 patients with NTM of 12 different neoplastic entities using the IVDR-certified M371-Test for quantitative real-time PCR. Median M371 serum levels and percentages of M371 level elevations were calculated for the entire NTM group and for entity-specific subgroups. The results were compared with GCT patients (n = 20) and with tumour-free male controls (n = 20) using descriptive statistical methods.

resultsEight patients with NTMs had M371 serum level elevations, corresponding to a false-positive rate (FPR) of 5.84% (95% confidence intervals (CIs) 2.55-11.18%). Expression rates in GCTs and controls were 100% and zero, respectively. Thus, the specificity of the M371-Test for GCT is 94.90% (95% CI 90.21-97.77%) when all NTMs and tumour-free controls are considered. Remarkably, three out of 5 patients with multiple myeloma had elevated M371 levels.

conclusionThe false-positive rate of the M371-Test in other malignancies than GCT is very low, and almost identical with that in healthy males, corresponding to a high specificity of 94.9% for detection of GCT. The surprising finding of M371 elevations in patients with multiple myeloma needs further investigation.

Indexed as

Biomarkers, TumorMicroRNAsNeoplasmsNeoplasms, Germ Cell and EmbryonalAdolescentAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedTesticular NeoplasmsYoung AdultBiomarkers, TumorMicroRNAsMIRN371 microRNA, humanBiomarkerChromosome 19, test specificitymicroRNA-371a-3pMultiple myelomaTesticular germ cell tumour

Identifiers

PMID39888414
PMCPMC11785664

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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.