Aragon Han Patricia, Weng Chien-Hsiang, Khawaja Hunain T, Nagarajan Neeraja, Schneider Eric B, Umbricht Christopher B, Witwer Kenneth W, Zeiger Martha A
1 Endocrine Surgery Section, Department of Surgery, The Johns Hopkins University School of Medicine , Baltimore, Maryland.
2 Johns Hopkins Surgery Center for Outcomes Research, Department of Surgery, The Johns Hopkins University School of Medicine , Baltimore, Maryland.
Thyroid. 2015 Dec;25(12):1322-9. doi: 10.1089/thy.2015.0193. Epub 2015 Oct 8.
Studies have suggested that microRNAs (miR) may be useful prognostic markers and are associated with aggressive clinicopathologic features in papillary thyroid cancer (PTC). This systematic review examined associations between miRs and aggressive clinicopathologic features in PTC.
A literature search was performed within the PubMed, Embase, Cochrane, Web of Science, and Scopus databases for papers published prior to November 24, 2014. The search was performed by combining the concepts "thyroid tumor" with "microRNA" and by using "and" as the Boolean operator. Upon retrieval of candidate studies, full-text publications were reviewed in their entirety and selected if they examined the prognostic significance between miR expression and established aggressive clinicopathologic features of PTC.
Fifteen studies from 13 unique groups that included 807 patients were reviewed. Most of the studies were retrospective, and none included patients who had undergone routine central lymph node dissection. Expression levels of miRs-21, -34b, -130b, -135b, -146b, -151, -181b, -199b-5p, -221, -222, -451, -623, -1271, -2861, and let-7e showed significant association with at least one aggressive feature, such as large tumor size, extrathyroidal extension, multifocality, lymphovascular invasion, lymph node metastases, distant metastasis, advanced American Joint Cancer Committee stage, and presence of the BRAF(V600E) mutation. Herein we summarize the literature with regard to these associations.
Further studies are needed to investigate whether miRs are independent predictors of aggressive clinicopathologic features before it can be recommended that miR expression levels should be incorporated into the management algorithm for patients with PTC. A well-designed prospective study is needed to assess these potential associations.
研究表明,微小RNA(miR)可能是有用的预后标志物,并且与甲状腺乳头状癌(PTC)的侵袭性临床病理特征相关。本系统评价研究了miR与PTC侵袭性临床病理特征之间的关联。
在PubMed、Embase、Cochrane、Web of Science和Scopus数据库中检索2014年11月24日前发表的论文。通过将“甲状腺肿瘤”与“微小RNA”的概念相结合,并使用“与”作为布尔运算符进行检索。检索到候选研究后,对全文进行全面审查,如果研究探讨了miR表达与PTC既定侵袭性临床病理特征之间的预后意义,则予以入选。
对来自13个独立研究小组的15项研究进行了综述,共纳入807例患者。大多数研究为回顾性研究,且均未纳入接受常规中央淋巴结清扫的患者。miR-21、-34b、-130b、-135b、-146b、-151、-181b、-199b-5p、-221、-222、-451、-623、-1271、-2861和let-7e的表达水平与至少一种侵袭性特征显著相关,如肿瘤体积大、甲状腺外侵犯、多灶性、淋巴管侵犯、淋巴结转移、远处转移、美国癌症联合委员会分期高以及BRAF(V600E)突变的存在。在此,我们总结了关于这些关联的文献。
在建议将miR表达水平纳入PTC患者的管理算法之前,需要进一步研究以调查miR是否为侵袭性临床病理特征的独立预测因子。需要进行精心设计的前瞻性研究来评估这些潜在关联。