Department of Growth and Reproduction, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Nat Rev Urol. 2020 Apr;17(4):201-213. doi: 10.1038/s41585-020-0296-x. Epub 2020 Mar 10.
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.
睾丸生殖细胞肿瘤(TGCTs)是年轻男性最常见的癌症类型,起源于常见的前体细胞生殖细胞原位肿瘤(GCNIS)。几十年来,TGCT 患者的临床管理一直依赖于经典的血清肿瘤标志物:甲胎蛋白、人绒毛膜促性腺激素亚单位-β 和乳酸脱氢酶。在过去的 10 年中,microRNAs 已被证明在原发性肿瘤的诊断以及随访监测和复发预测方面优于经典的血清肿瘤标志物。miR-371a-3p 是最一致的标志物,在 TGCT 中具有超过 90%的诊断灵敏度和特异性。然而,miR-371a-3p 不能用于诊断 GCNIS 或成熟畸胎瘤。未来的工作必须在技术上实现基于 microRNA 的方法的国际标准化,并将 miR-371a-3p 作为一种基于分子液体活检的 TGCT 标志物引入临床。