R. Harun, J. Hadi, Nur Shukriyah Mhazir, Pang Jyh Chyang, I. Rose, R. Manap, F. Anshar, NorAdina A Tajuddin, Andrea By Li, A Rahman A Jamal
{"title":"基因表达谱预测晚期非小细胞肺癌患者的生存","authors":"R. Harun, J. Hadi, Nur Shukriyah Mhazir, Pang Jyh Chyang, I. Rose, R. Manap, F. Anshar, NorAdina A Tajuddin, Andrea By Li, A Rahman A Jamal","doi":"10.1109/ICMSAO.2011.5775581","DOIUrl":null,"url":null,"abstract":"A large variation in prognosis is observed despite the use of clinical prognostic factors in patients with advanced non-small cell lung cancer (NSCLC). It is likely that this variation is due to the different biological properties of the tumour cells. In this work we aimed to identify gene signature that could predict survival in advanced NSCLC. Total RNA was extracted from five 5 μm-thick sections of the FFPE using the High Pure RNA Paraffin Kit (Roche). RNA amplification was performed using WT-Ovation™ FFPE RNA Amplification System V2 (NuGen). The amplified cDNA was then labelled and hybridised onto Illumina HumanRef-8 v3.0 Expression BeadChips. Microarray data analysis was subsequently performed using Genespring GX version 9.0. Out of 75 FFPE samples, only 32 had sufficient RNA quality and quantity for microarray gene expression analysis. Patients were grouped into long and short survival groups based on the time to cancer-related death. After normalization and filtration, 19,002 genes were selected for differential gene expression analysis. A total of 440 genes differed significantly between the long and short survival groups (ANOVA, p < 0.05, with Benjamini and Hochberg False Discovery Rate multiple testing correction). Unsupervised Hierarchial Clustering with Pearson correlation and average linkage identified two broad clusters of patients corresponding to the long and short survival. Thirteen genes were selected based on the TTest, 2-fold expression changes, principal components analysis and univariate Cox regression analysis and risk scores were calculated for each patient. These gene signatures were independent predictors of survival. The model was validated with a published microarray data from 130 patients with NSCLC. Using Gene Set Analysis (GSA), we found certain biological processes including metastasis and chemotherapy resistance were up-regulated in the short survival group while TID pathway and MAPKKK cascade were enriched in the long survival group. As the conclusion, there is several distinct gene expression profiles associated with survival of patients with advanced stage NSCLC. 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引用次数: 2
摘要
尽管在晚期非小细胞肺癌(NSCLC)患者中使用了临床预后因素,但观察到预后存在很大差异。这种差异很可能是由于肿瘤细胞的不同生物学特性。在这项工作中,我们旨在确定可以预测晚期非小细胞肺癌生存的基因特征。采用高纯度RNA石蜡试剂盒(Roche)从5个5 μm厚的FFPE切片中提取总RNA。采用WT-Ovation™FFPE RNA扩增系统V2 (NuGen)进行RNA扩增。然后将扩增的cDNA标记并杂交到Illumina HumanRef-8 v3.0表达珠芯片上。随后使用genesspring GX version 9.0进行微阵列数据分析。在75个FFPE样本中,只有32个样本具有足够的RNA质量和数量进行微阵列基因表达分析。根据癌症相关死亡的时间,将患者分为长生存组和短生存组。经归一化和过滤后,选择19,002个基因进行差异基因表达分析。长生存组和短生存组共有440个基因差异显著(方差分析,p < 0.05,经Benjamini和Hochberg错误发现率多重检验校正)。无监督分层聚类与Pearson相关和平均连锁确定了两大类患者对应的长生存期和短生存期。根据TTest选择13个基因,进行2倍表达变化、主成分分析和单因素Cox回归分析,计算每位患者的风险评分。这些基因特征是生存的独立预测因子。该模型用来自130例非小细胞肺癌患者的公开微阵列数据进行了验证。通过基因集分析(Gene Set Analysis, GSA),我们发现短生存组的转移和化疗耐药等生物学过程上调,而长生存组的TID通路和MAPKKK级联富集。综上所述,有几种不同的基因表达谱与晚期NSCLC患者的生存相关。晚期非小细胞肺癌的生存结果可以基于13个基因特征来预测。
Gene expression profiles predict survival of patients with advanced non-small cell lung cancers
A large variation in prognosis is observed despite the use of clinical prognostic factors in patients with advanced non-small cell lung cancer (NSCLC). It is likely that this variation is due to the different biological properties of the tumour cells. In this work we aimed to identify gene signature that could predict survival in advanced NSCLC. Total RNA was extracted from five 5 μm-thick sections of the FFPE using the High Pure RNA Paraffin Kit (Roche). RNA amplification was performed using WT-Ovation™ FFPE RNA Amplification System V2 (NuGen). The amplified cDNA was then labelled and hybridised onto Illumina HumanRef-8 v3.0 Expression BeadChips. Microarray data analysis was subsequently performed using Genespring GX version 9.0. Out of 75 FFPE samples, only 32 had sufficient RNA quality and quantity for microarray gene expression analysis. Patients were grouped into long and short survival groups based on the time to cancer-related death. After normalization and filtration, 19,002 genes were selected for differential gene expression analysis. A total of 440 genes differed significantly between the long and short survival groups (ANOVA, p < 0.05, with Benjamini and Hochberg False Discovery Rate multiple testing correction). Unsupervised Hierarchial Clustering with Pearson correlation and average linkage identified two broad clusters of patients corresponding to the long and short survival. Thirteen genes were selected based on the TTest, 2-fold expression changes, principal components analysis and univariate Cox regression analysis and risk scores were calculated for each patient. These gene signatures were independent predictors of survival. The model was validated with a published microarray data from 130 patients with NSCLC. Using Gene Set Analysis (GSA), we found certain biological processes including metastasis and chemotherapy resistance were up-regulated in the short survival group while TID pathway and MAPKKK cascade were enriched in the long survival group. As the conclusion, there is several distinct gene expression profiles associated with survival of patients with advanced stage NSCLC. Survival outcomes in advanced NSCLC could be predicted based on a 13-gene signature.