Abstract
Testicular germ cell tumours (TGCTs) are the most frequent cancer type in young men and originate from the common precursor germ cell neoplasia in situ (GCNIS). For decades, clinical management of patients with TGCT has relied on classic serum tumour markers: α-fetoprotein, human chorionic gonadotropin subunit-β and lactate dehydrogenase. In the past 10 years, microRNAs have been shown to outperform classic serum tumour markers in the diagnosis of primary tumours and in follow-up monitoring and prediction of relapse. miR-371a-3p is the most consistent marker and exhibits >90% diagnostic sensitivity and specificity in TGCT. However, miR-371a-3p cannot be used to diagnose GCNIS or mature teratoma. Future efforts must technically standardize the microRNA-based methods internationally and introduce miR-371a-3p as a molecular liquid biopsy-based marker for TGCTs in the clinic.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Aftercare
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Biomarkers, Tumor / genetics
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Biomarkers, Tumor / metabolism*
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Chorionic Gonadotropin, beta Subunit, Human / metabolism
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Humans
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L-Lactate Dehydrogenase / metabolism
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Liquid Biopsy
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Male
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MicroRNAs / metabolism*
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Neoplasm Recurrence, Local / diagnosis*
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Neoplasm Recurrence, Local / metabolism
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Neoplasms, Germ Cell and Embryonal / diagnosis*
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Neoplasms, Germ Cell and Embryonal / genetics
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Neoplasms, Germ Cell and Embryonal / metabolism
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Neoplasms, Germ Cell and Embryonal / therapy
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Seminoma / diagnosis
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Seminoma / genetics
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Seminoma / metabolism
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Seminoma / therapy
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Sensitivity and Specificity
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Teratoma / diagnosis
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Teratoma / genetics
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Teratoma / metabolism
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Teratoma / therapy
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Testicular Neoplasms / diagnosis*
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Testicular Neoplasms / genetics
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Testicular Neoplasms / metabolism
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Testicular Neoplasms / therapy
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alpha-Fetoproteins / metabolism
Substances
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Biomarkers, Tumor
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Chorionic Gonadotropin, beta Subunit, Human
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MIRN302A microRNA, human
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MIRN367 microRNA, human
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MIRN371 microRNA, human
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MIRN372 microRNA, human
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MIRN373 microRNA, human
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MicroRNAs
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alpha-Fetoproteins
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L-Lactate Dehydrogenase