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Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm

机译:使用微阵列 - 基因集减量算法的显着分析非小细胞肺癌的分类

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Among non-small cell lung cancer (NSCLC), adenocarcinoma (AC), and squamous cell carcinoma (SCC) are two major histology subtypes, accounting for roughly 40% and 30% of all lung cancer cases, respectively. Since AC and SCC differ in their cell of origin, location within the lung, and growth pattern, they are considered as distinct diseases. Gene expression signatures have been demonstrated to be an effective tool for distinguishing AC and SCC. Gene set analysis is regarded as irrelevant to the identification of gene expression signatures. Nevertheless, we found that one specific gene set analysis method, significance analysis of microarraygene set reduction (SAMGSR), can be adopted directly to select relevant features and to construct gene expression signatures. In this study, we applied SAMGSR to a NSCLC gene expression dataset. When compared with several novel feature selection algorithms, for example, LASSO, SAMGSR has equivalent or better performance in terms of predictive ability and model parsimony. Therefore, SAMGSR is a feature selection algorithm, indeed. Additionally, we applied SAMGSR to AC and SCC subtypes separately to discriminate their respective stages, that is, stage II versus stage I. Few overlaps between these two resulting gene signatures illustrate that AC and SCC are technically distinct diseases. Therefore, stratified analyses on subtypes are recommended when diagnostic or prognostic signatures of these two NSCLC subtypes are constructed.
机译:在非小细胞肺癌(NSCLC)中,腺癌(AC)和鳞状细胞癌(SCC)分别是两个主要的组织学亚型,分别占所有肺癌病例的约40%和30%。由于AC和SCC在它们的起源细胞中不同,因此肺部内的位置和生长模式,它们被认为是不同的疾病。已经证明基因表达签名是区分AC和SCC的有效工具。基因集分析被认为与基因表达签名的鉴定无关。然而,我们发现一种特定的基因设定分析方法,微arraygene集合减少(SAMGSR)的显着性分析,可以直接采用,以选择相关特征和构建基因表达签名。在本研究中,我们将Samgsr应用于NSCLC基因表达数据集。例如,与几个新颖的特征选择算法相比,例如套索,SAMGSR在预测能力和模型定义方面具有等同的或更好的性能。因此,Samgsr是一个特征选择算法,实际上。此外,我们将SAMGSR应用于AC和SCC亚型,以区分其各自的阶段,即阶段II与阶段I.这两个结果基因签名之间几乎没有重叠,说明AC和SCC是技术上不同的疾病。因此,当构建这两个NSCLC亚型的诊断或预后签名时,建议在亚型上进行分层分析。

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