Department of Urology, Rush University Medical Center, Chicago, IL 60612-3833, USA.
Department of Urology, University of Verona, 37126 Verona, Italy.
Medicina (Kaunas). 2023 Nov 17;59(11):2033. doi: 10.3390/medicina59112033.
: Despite advancements in the diagnosis and treatment of testicular germ cell tumours (TGTCs), challenges persist in identifying reliable biomarkers for early detection and precise disease management. This narrative review addresses the role of microRNAs (miRNAs) as potential diagnostic tools and therapeutic targets in the treatment of TGCTs. : Three databases (PubMed, Web of Science™, and Scopus) were queried for studies investigating the utility of miRNA as diagnostic tools, assessing their prognostic significance, and evaluating their potential to guide TGCT treatment. Different combinations of the following keywords were used, according to a free-text protocol: "miRNA", "non-coding RNA", "small RNA", "Testicular Cancer", "seminomatous testicular germ cell", "non-seminomatous testicular germ cell". : The potential of miRNAs as possible biomarkers for a non-invasive diagnosis of TGCT is appealing. Their integration into the diagnostic pathway for TGCT patients holds the potential to enhance the discriminative power of conventional serum tumour markers (STMs) and could expedite early diagnosis, given that miRNA overexpression was observed in 50% of GCNIS cases. Among miRNAs, miR-371a-3p stands out with the most promising evidence, suggesting its relevance in the primary diagnosis of TGCT, particularly when conventional STMs offer limited value. Indeed, it demonstrated high specificity (90-99%) and sensitivity (84-89%), with good positive predictive value (97.2%) and negative predictive value (82.7%). Furthermore, a direct relationship between miRNA concentration, disease burden, and treatment response exists, regardless of disease stages. The initial evidence of miRNA decrease in response to surgical treatment and systemic chemotherapy has been further supported by more recent results suggesting the potential utility of this tool not only in evaluating treatment response but also in monitoring residual disease and predicting disease relapse. : MiRNAs could represent a reliable tool for accurate diagnosis and disease monitoring in the treatment of TGCT, providing more precise tools for early detection and treatment stratification. Nevertheless, well-designed clinical trials and comprehensive long-term data are needed to ensure their translation into effective clinical tools.
尽管在睾丸生殖细胞肿瘤(TGCTs)的诊断和治疗方面取得了进展,但在确定可靠的生物标志物以进行早期检测和精确疾病管理方面仍然存在挑战。本叙述性综述探讨了 microRNAs(miRNAs)作为潜在诊断工具和治疗靶点在 TGCT 治疗中的作用。
我们在三个数据库(PubMed、Web of Science™和 Scopus)中检索了研究 miRNA 作为诊断工具的效用、评估其预后意义以及评估其指导 TGCT 治疗潜力的研究。根据自由文本方案,使用了以下关键词的不同组合:“miRNA”、“非编码 RNA”、“small RNA”、“Testicular Cancer”、“seminomatous testicular germ cell”、“non-seminomatous testicular germ cell”。
miRNAs 作为 TGCT 非侵入性诊断的潜在生物标志物具有吸引力。将其纳入 TGCT 患者的诊断途径有可能提高传统血清肿瘤标志物(STMs)的鉴别能力,并有可能加快早期诊断,因为在 50%的 GCNIS 病例中观察到 miRNA 过表达。在 miRNA 中,miR-371a-3p 具有最有前途的证据,表明其在 TGCT 的原发性诊断中具有相关性,特别是在常规 STMs 价值有限时。事实上,它表现出高特异性(90-99%)和敏感性(84-89%),具有良好的阳性预测值(97.2%)和阴性预测值(82.7%)。此外,miRNA 浓度与疾病负担和治疗反应之间存在直接关系,无论疾病阶段如何。miRNA 在手术治疗和全身化疗后减少的初步证据得到了最近结果的进一步支持,这些结果表明该工具不仅在评估治疗反应方面具有潜在的效用,而且在监测残留疾病和预测疾病复发方面也具有潜在的效用。
miRNAs 可能成为 TGCT 治疗中准确诊断和疾病监测的可靠工具,为早期检测和治疗分层提供更精确的工具。然而,需要进行精心设计的临床试验和全面的长期数据,以确保将其转化为有效的临床工具。