Cargando…

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

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lei, Wang, Linlin, Du, Bochuan, Wang, Tianjiao, Tian, Pu, Tian, Suyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944087/
https://www.ncbi.nlm.nih.gov/pubmed/27446945
http://dx.doi.org/10.1155/2016/2491671
_version_ 1782442707384270848
author Zhang, Lei
Wang, Linlin
Du, Bochuan
Wang, Tianjiao
Tian, Pu
Tian, Suyan
author_facet Zhang, Lei
Wang, Linlin
Du, Bochuan
Wang, Tianjiao
Tian, Pu
Tian, Suyan
author_sort Zhang, Lei
collection PubMed
description 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 microarray-gene 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.
format Online
Article
Text
id pubmed-4944087
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-49440872016-07-21 Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm Zhang, Lei Wang, Linlin Du, Bochuan Wang, Tianjiao Tian, Pu Tian, Suyan Biomed Res Int Research Article 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 microarray-gene 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. Hindawi Publishing Corporation 2016 2016-06-30 /pmc/articles/PMC4944087/ /pubmed/27446945 http://dx.doi.org/10.1155/2016/2491671 Text en Copyright © 2016 Lei Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Lei
Wang, Linlin
Du, Bochuan
Wang, Tianjiao
Tian, Pu
Tian, Suyan
Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title_full Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title_fullStr Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title_full_unstemmed Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title_short Classification of Non-Small Cell Lung Cancer Using Significance Analysis of Microarray-Gene Set Reduction Algorithm
title_sort classification of non-small cell lung cancer using significance analysis of microarray-gene set reduction algorithm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944087/
https://www.ncbi.nlm.nih.gov/pubmed/27446945
http://dx.doi.org/10.1155/2016/2491671
work_keys_str_mv AT zhanglei classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm
AT wanglinlin classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm
AT dubochuan classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm
AT wangtianjiao classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm
AT tianpu classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm
AT tiansuyan classificationofnonsmallcelllungcancerusingsignificanceanalysisofmicroarraygenesetreductionalgorithm