Silaghi Cristina Alina, Lozovanu Vera, Silaghi Horatiu, Georgescu Raluca Diana, Pop Cristina, Dobrean Anca, Georgescu Carmen Emanuela
Department of Endocrinology, "Iuliu Hatieganu" University of Medicine and Pharmacy Cluj-Napoca, Victor Babes Street 8, 400012 Cluj-Napoca, Romania.
Department of Surgery V, "Iuliu Hatieganu" University of Medicine and Pharmacy Cluj-Napoca, Victor Babes Street 8, 400012 Cluj-Napoca, Romania.
Cancers (Basel). 2020 Sep 12;12(9):2608. doi: 10.3390/cancers12092608.
Thyroid cancer (TC) includes various phenotypes, from indolent to highly aggressive cancer. The limitations of the current prognostication systems to predict the recurrence risk and the variability in expression of the genes involved in the thyroid carcinogenesis uncover the need for new prognostic biomarkers by taking into account potential epigenetic differences. We aimed to summarize the current knowledge regarding the prognostic impact of microRNAs (miRNAs) in TC. A literature search was conducted in PubMed, Embase, Scopus, and Web of Science databases. Both upregulated and downregulated miRNAs are significantly correlated with worse overall survival (hazard ratio (HR) = 5.94, 95% CI: 2.73-12.90, < 0.001; HR = 0.51, 95% CI: 0.26-0.96, = 0.048) disease/recurrence-free survival (HR = 1.58, 95% CI: 1.08-2.32, = 0.003; HR = 0.37, 95%, CI: 0.24-0.60, < 0.001). Sensitivity analysis revealed a significant association between the higher expression of miR-146b, miR-221, and miR-222 and the recurrence of papillary TC (OR = 9.11, 95% CI 3.00 to 27.52; < 0.001; OR = 3.88, 95% CI 1.34 to 11.19, < 0.001; OR = 6.56, 95% CI 2.75 to 15.64, < 0.001). This research identified that miR-146b, miR-221, and miR-222 could serve as potential prognostic biomarkers in TC, particularly in PTC. Further studies are needed to strengthen these findings and sustain its clinical applicability.
甲状腺癌(TC)包括从惰性到高度侵袭性的各种表型。当前预测复发风险的预后系统存在局限性,且甲状腺癌发生过程中涉及的基因表达存在变异性,这表明需要通过考虑潜在的表观遗传差异来寻找新的预后生物标志物。我们旨在总结目前关于微小RNA(miRNA)在甲状腺癌中的预后影响的知识。在PubMed、Embase、Scopus和Web of Science数据库中进行了文献检索。上调和下调的miRNA均与较差的总生存期(风险比(HR)= 5.94,95%置信区间:2.73 - 12.90,P < 0.001;HR = 0.51,95%置信区间:0.26 - 0.96,P = 0.048)、疾病/无复发生存期(HR = 1.58,95%置信区间:1.08 - 2.32,P = 0.003;HR = 0.37,95%置信区间:0.24 - 0.60,P < 0.001)显著相关。敏感性分析显示,miR - 146b、miR - 221和miR - 222的高表达与乳头状甲状腺癌的复发之间存在显著关联(比值比(OR)= 9.11,95%置信区间3.00至27.52;P < 0.001;OR = 3.88,95%置信区间1.34至11.19,P < 0.001;OR = 6.56,95%置信区间2.75至15.64,P < 0.001)。本研究确定miR - 146b、miR - 221和miR - 222可作为甲状腺癌,特别是乳头状甲状腺癌潜在的预后生物标志物。需要进一步研究来加强这些发现并维持其临床适用性。