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低分化甲状腺癌的 microRNA 谱:新的诊断和预后见解。

MicroRNA profile of poorly differentiated thyroid carcinomas: new diagnostic and prognostic insights.

机构信息

Department of Pathology and Laboratory Medicine, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA Institute of Pathology, University of Bern, Murtenstrasse 31, 3010 Bern, Switzerland Institute of Surgical Pathology, University Hospital Zurich, 8091 Zurich, Switzerland Institute of Surgical Pathology, Triemlispital Zurich, 8063 Zurich, Switzerland.

出版信息

J Mol Endocrinol. 2014 Mar 6;52(2):181-9. doi: 10.1530/JME-13-0266. Print 2014 Apr.

Abstract

The diagnosis of conventional and oncocytic poorly differentiated (oPD) thyroid carcinomas is difficult. The aim of this study is to characterise their largely unknown miRNA expression profile and to compare it with well-differentiated thyroid tumours, as well as to identify miRNAs which could potentially serve as diagnostic and prognostic markers. A total of 14 poorly differentiated (PD), 13 oPD, 72 well-differentiated thyroid carcinomas and eight normal thyroid specimens were studied for the expression of 768 miRNAs using PCR-Microarrays. MiRNA expression was different between PD and oPD thyroid carcinomas, demonstrating individual clusters on the clustering analysis. Both tumour types showed upregulation of miR-125a-5p, -15a-3p, -182, -183-3p, -222, -222-5p, and downregulation of miR-130b, -139-5p, -150, -193a-5p, -219-5p, -23b, -451, -455-3p and of miR-886-3p as compared with normal thyroid tissue. In addition, the oPD thyroid carcinomas demonstrated upregulation of miR-221 and miR-885-5p. The difference in expression was also observed between miRNA expression in PD and well-differentiated tumours. The CHAID algorithm allowed the separation of PD from well-differentiated thyroid carcinomas with 73-79% accuracy using miR-23b and miR-150 as a separator. Kaplan-Meier and multivariate analysis showed a significant association with tumour relapses (for miR-23b) and with tumour-specific death (for miR-150) in PD and oPD thyroid carcinomas. MiRNA expression is different in conventional and oPD thyroid carcinomas in comparison with well-differentiated thyroid cancers and can be used for discrimination between these tumour types. The newly identified deregulated miRNAs (miR-150, miR-23b) bear the potential to be used in a clinical setting, delivering prognostic and diagnostic informations.

摘要

常规和嗜酸细胞性低分化(oPD)甲状腺癌的诊断较为困难。本研究旨在描述其大部分未知的 miRNA 表达谱,并将其与分化良好的甲状腺肿瘤进行比较,同时确定可能作为诊断和预后标志物的 miRNA。使用 PCR-Microarrays 对 14 例低分化(PD)、13 例嗜酸细胞性低分化、72 例分化良好的甲状腺癌和 8 例正常甲状腺标本进行了 768 个 miRNA 的表达研究。聚类分析显示,PD 和 oPD 甲状腺癌之间的 miRNA 表达存在差异,表现为个体聚类。两种肿瘤类型均表现出 miR-125a-5p、-15a-3p、-182、-183-3p、-222、-222-5p 的上调,miR-130b、-139-5p、-150、-193a-5p、-219-5p、-23b、-451、-455-3p 和 miR-886-3p 的下调。此外,oPD 甲状腺癌表现出 miR-221 和 miR-885-5p 的上调。PD 与分化良好的肿瘤之间的 miRNA 表达也存在差异。CHAID 算法使用 miR-23b 和 miR-150 作为分离器,可将 PD 与分化良好的甲状腺癌区分开来,准确率为 73-79%。Kaplan-Meier 和多变量分析显示,miR-23b 与 PD 和 oPD 甲状腺癌的肿瘤复发显著相关,miR-150 与肿瘤特异性死亡显著相关。与分化良好的甲状腺癌相比,常规和嗜酸细胞性低分化甲状腺癌的 miRNA 表达不同,可用于区分这些肿瘤类型。新发现的失调 miRNA(miR-150、miR-23b)具有在临床环境中使用的潜力,提供预后和诊断信息。

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