用寡核苷酸芯片分析韩国患者甲状腺乳头状癌的基因表达谱。

Journal of the Korean Surgical Society Pub Date : 2012-05-01 Epub Date: 2012-04-26 DOI:10.4174/jkss.2012.82.5.271
Ki-Wook Chung, Seok Won Kim, Sun Wook Kim
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引用次数: 22

摘要

目的:在韩国,甲状腺乳头状癌(ptc)的发病率正在迅速上升。分析ptc的基因表达谱(GEP)将促进诊断、预后和治疗新方法的出现。我们进行这项研究是为了找出韩国ptc的GEP。方法:对19例ptc和7例正常甲状腺进行寡核苷酸芯片分析。差异表达基因选择采用t检验(|fold| >3),调整benjamin - hochberg错误发现率p值< 0.01。采用定量逆转录聚合酶链反应(QRT-PCR)验证微阵列数据。采用支持向量机(SVM)算法建立了基于分子特征的ptc诊断分类模型。结果:根据标准鉴定出79个差异表达基因(上调70个,下调9个)。5个基因(CDH3, NGEF, PROS1, TGFA, MET)的QRT-PCR验证了微阵列数据。基于GEP的分层聚类分析和支持向量机算法的分类模型能准确区分ptc与正常甲状腺。结论:疾病分类模型对ptc的诊断具有良好的准确性,为分子诊断提供了可能。该GEP可作为基于分子特征的ptc管理进一步研究的基线数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gene expression profiling of papillary thyroid carcinomas in Korean patients by oligonucleotide microarrays.

Purpose: The incidence of papillary thyroid carcinomas (PTCs) is rapidly increasing in Korea. Analyzing the gene expression profiling (GEP) of PTCs will facilitate the advent of new methods in diagnosis, prognostication, and treatment. We performed this study to find the GEP of Korean PTCs.

Methods: We performed oligonucleotide microarray analysis with 19 PTCs and 7 normal thyroid glands. Differentially expressed genes were selected using a t-test (|fold| >3) and adjusted Benjamini-Hochberg false discovery rate P-value < 0.01. Quantitative reverse transcription-polymerase chain reaction (QRT-PCR) was used to validate microarray data. A classification model was developed by support vector machine (SVM) algorithm to diagnose PTCs based on molecular signatures.

Results: We identified 79 differentially expressed genes (70 up-regulated and 9 down-regulated) according to the criteria. QRT-PCR for five genes (CDH3, NGEF, PROS1, TGFA, MET) was confirmatory of the microarray data. Hierarchical cluster analysis and a classification model by the SVM algorithm accurately differentiated PTCs from normal thyroid gland based on GEP.

Conclusion: A disease classification model showed excellent accuracy in diagnosing PTCs, thus showing the possibility of molecular diagnosis in the future. This GEP could serve as baseline data for further investigation in the management of PTCs based on molecular signatures.

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