» Articles » PMID: 25187505

MicroRNA MiR-371a-3p in Serum of Patients with Germ Cell Tumours: Evaluations for Establishing a Serum Biomarker

Overview
Journal Andrology
Date 2014 Sep 5
PMID 25187505
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

As only 60% of the patients with germ cell tumour (GCT) express the classical markers, new markers as for example microRNAs (miRNAs) are required. One promising candidate is miR-371a-3p, but data are sparse to date. We measured serum levels of miR-371a-3p in GCT patients, in controls, and in cases with other malignancies. We also assessed the expression in other body fluids and we looked to the decline of serum miR-371a-3p levels after treatment. miR-371a-3p levels were measured by quantitative polymerase chain reaction in serum samples of 25 GCT patients, 6 testicular intraepithelial neoplasia (TIN) patients, 20 healthy males and 24 non-testicular malignancies (NTMs). Testicular vein blood (TVB) was examined in five GCT patients and five controls. Five GCT patients had serial daily measurements after orchiectomy. Five seminal plasma samples, three urine specimens and one pleural effusion fluid were processed likewise. GCT patients had significantly higher miR-371a-3p serum levels than controls and NTMs. Serum levels of controls, TINs and NTMs were not significantly different. TVB samples of GCT patients had 65.4-fold higher serum levels than peripheral blood. Malignant pleural effusion fluid had extremely high levels of miR-371a-3p, seminal plasma had strongly elevated levels by comparison with serum levels of controls. In urine of GCT patients, no miR-371a-3p expression was detected. Daily measurements after orchiectomy in stage 1 patients revealed a decline by 95% within 24 h. Serum levels of miR-371a-3p appear to be a promising specific biomarker of GCTs as is suggested by high serum levels in GCT patients, the rapid return of elevated levels to normal range after treatment, the association of serum levels with tumour bulk, the non-expression in NTMs and the much higher levels of miR-371a-3p in TVB. This potential marker deserves further exploration in a large-scale clinical study.

Citing Articles

Analysis of a mouse germ cell tumor model establishes pluripotency-associated miRNAs as conserved serum biomarkers for germ cell cancer detection.

Loehr A, Timmerman D, Liu M, Gillis A, Matthews M, Bloom J Sci Rep. 2025; 15(1):4452.

PMID: 39910147 PMC: 11799207. DOI: 10.1038/s41598-025-88554-8.


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

Belge G, Klemke M, Hansen B, Dumlupinar C, Igde A, Arnold D J Cancer Res Clin Oncol. 2025; 151(2):58.

PMID: 39888414 PMC: 11785664. DOI: 10.1007/s00432-025-06101-4.


Spinal Metastases in Non-Seminomatous Germ Cell Testicular Tumors: Prognosis and Integrated Therapeutic Approaches-A Systematic Review with an Institutional Case Illustration.

Scalia G, Ferini G, Shams Z, Graziano F, Ponzo G, Giurato E Curr Oncol. 2024; 31(12):7459-7475.

PMID: 39727674 PMC: 11674372. DOI: 10.3390/curroncol31120551.


Potential next generation markers of testicular germ cell tumors: miRNA-371a-3p.

Zujuan S, Xin D, Yang H, Guifu Z Int Urol Nephrol. 2024; 57(3):691-700.

PMID: 39576421 DOI: 10.1007/s11255-024-04284-2.


Integrated bioinformatics analysis for exploring potential biomarkers related to Parkinson's disease progression.

Huang Z, Song E, Chen Z, Yu P, Chen W, Lin H BMC Med Genomics. 2024; 17(1):133.

PMID: 38760670 PMC: 11100188. DOI: 10.1186/s12920-024-01885-9.