Department of Surgery, Section of Endocrine Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Ann Surg Oncol. 2011 Jul;18(7):2035-41. doi: 10.1245/s10434-011-1733-0. Epub 2011 May 3.
Papillary thyroid carcinoma (PTC) has relatively indolent behavior, although some tumors recur and disseminate to distant sites. The aggressive biological behavior of PTC is difficult to predict. MicroRNAs (miRNAs) are dysregulated in various tumors types, and some of them serve as markers of poor prognosis. In this study, we evaluated miRNA expression as a marker of more aggressive behavior in PTC.
miRNA array was used to identify a subset of differentially expressed miRNAs between aggressive and nonaggressive PTC. These miRNAs were further validated by real-time RT-PCR in a cohort of 17 PTC with local tumor recurrence or distant metastases and 15 PTC with no extrathyroidal dissemination and correlated with BRAF, RAS, and RET/PTC mutations and MET expression.
The miRNA array identified miR-146b, miR-221, miR-222, miR-155, miR-31 upregulation and miR-1, miR-34b, miR-130b, miR-138 downregulation in aggressive compared with nonaggressive PTC. Significant miRNA deregulation was confirmed in the validation cohort, with upregulation of miR-146b and miR-222 and downregulation of miR-34b and miR-130b seen in aggressive PTC. Among BRAF-positive tumors, miR-146b showed strong association with aggressive PTC. MET was identified as a potential target gene for 2 downregulated miRNAs (miR-34b and miR-1), and significantly higher level of MET expression was observed in aggressive PTC.
We demonstrate that miR-146b, miR-222, miR-34b, miR-130b are differentially expressed in aggressive compared with nonaggressive PTC. Among BRAF-positive tumors, overexpression of miR-146b was associated with aggressive behavior, suggesting that it may further refine the prognostic importance of BRAF.
甲状腺乳头状癌(PTC)的行为相对惰性,尽管有些肿瘤会复发并扩散到远处部位。PTC 的侵袭性生物学行为难以预测。microRNAs(miRNAs)在各种肿瘤类型中失调,其中一些可作为预后不良的标志物。在本研究中,我们评估了 miRNA 表达作为 PTC 侵袭性行为的标志物。
使用 miRNA 芯片鉴定侵袭性和非侵袭性 PTC 之间差异表达的 miRNA 子集。通过实时 RT-PCR 在 17 例局部肿瘤复发或远处转移和 15 例无甲状腺外播散的 PTC 中进一步验证这些 miRNA,并与 BRAF、RAS 和 RET/PTC 突变和 MET 表达相关。
miRNA 芯片鉴定出侵袭性 PTC 中 miR-146b、miR-221、miR-222、miR-155、miR-31 上调和 miR-1、miR-34b、miR-130b、miR-138 下调。在验证队列中证实了显著的 miRNA 失调,在侵袭性 PTC 中观察到 miR-146b 和 miR-222 的上调和 miR-34b 和 miR-130b 的下调。在 BRAF 阳性肿瘤中,miR-146b 与侵袭性 PTC 强烈相关。鉴定出 2 个下调 miRNA(miR-34b 和 miR-1)的潜在靶基因 MET,在侵袭性 PTC 中观察到 MET 表达水平显著升高。
我们证明 miR-146b、miR-222、miR-34b、miR-130b 在侵袭性 PTC 中与非侵袭性 PTC 相比表达不同。在 BRAF 阳性肿瘤中,miR-146b 的过表达与侵袭性行为相关,表明其可能进一步细化 BRAF 的预后意义。