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Partial least squares based gene expression analysis in renal failure
ABSTRACT: BACKGROUND: Preventive and therapeutic options for renal failure are still limited. Gene expression profile analysis is powerful in the identification of biological differences between end stage renal failure patients and healthy controls. Previous studies mainly used variance/regression a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104724/ https://www.ncbi.nlm.nih.gov/pubmed/24997640 http://dx.doi.org/10.1186/1746-1596-9-137 |
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author | Ding, Shuang Xu, Yinhai Hao, Tingting Ma, Ping |
author_facet | Ding, Shuang Xu, Yinhai Hao, Tingting Ma, Ping |
author_sort | Ding, Shuang |
collection | PubMed |
description | ABSTRACT: BACKGROUND: Preventive and therapeutic options for renal failure are still limited. Gene expression profile analysis is powerful in the identification of biological differences between end stage renal failure patients and healthy controls. Previous studies mainly used variance/regression analysis without considering various biological, environmental factors. The purpose of this study is to investigate the gene expression difference between end stage renal failure patients and healthy controls with partial least squares (PLS) based analysis. METHODS: With gene expression data from the Gene Expression Omnibus database, we performed PLS analysis to identify differentially expressed genes. Enrichment and network analyses were also carried out to capture the molecular signatures of renal failure. RESULTS: We acquired 573 differentially expressed genes. Pathway and Gene Ontology items enrichment analysis revealed over-representation of dysregulated genes in various biological processes. Network analysis identified seven hub genes with degrees higher than 10, including CAND1, CDK2, TP53, SMURF1, YWHAE, SRSF1, and RELA. Proteins encoded by CDK2, TP53, and RELA have been associated with the progression of renal failure in previous studies. CONCLUSIONS: Our findings shed light on expression character of renal failure patients with the hope to offer potential targets for future therapeutic studies. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1450799302127207 |
format | Online Article Text |
id | pubmed-4104724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41047242014-07-31 Partial least squares based gene expression analysis in renal failure Ding, Shuang Xu, Yinhai Hao, Tingting Ma, Ping Diagn Pathol Research ABSTRACT: BACKGROUND: Preventive and therapeutic options for renal failure are still limited. Gene expression profile analysis is powerful in the identification of biological differences between end stage renal failure patients and healthy controls. Previous studies mainly used variance/regression analysis without considering various biological, environmental factors. The purpose of this study is to investigate the gene expression difference between end stage renal failure patients and healthy controls with partial least squares (PLS) based analysis. METHODS: With gene expression data from the Gene Expression Omnibus database, we performed PLS analysis to identify differentially expressed genes. Enrichment and network analyses were also carried out to capture the molecular signatures of renal failure. RESULTS: We acquired 573 differentially expressed genes. Pathway and Gene Ontology items enrichment analysis revealed over-representation of dysregulated genes in various biological processes. Network analysis identified seven hub genes with degrees higher than 10, including CAND1, CDK2, TP53, SMURF1, YWHAE, SRSF1, and RELA. Proteins encoded by CDK2, TP53, and RELA have been associated with the progression of renal failure in previous studies. CONCLUSIONS: Our findings shed light on expression character of renal failure patients with the hope to offer potential targets for future therapeutic studies. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1450799302127207 BioMed Central 2014-07-05 /pmc/articles/PMC4104724/ /pubmed/24997640 http://dx.doi.org/10.1186/1746-1596-9-137 Text en Copyright © 2014 Ding et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ding, Shuang Xu, Yinhai Hao, Tingting Ma, Ping Partial least squares based gene expression analysis in renal failure |
title | Partial least squares based gene expression analysis in renal failure |
title_full | Partial least squares based gene expression analysis in renal failure |
title_fullStr | Partial least squares based gene expression analysis in renal failure |
title_full_unstemmed | Partial least squares based gene expression analysis in renal failure |
title_short | Partial least squares based gene expression analysis in renal failure |
title_sort | partial least squares based gene expression analysis in renal failure |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104724/ https://www.ncbi.nlm.nih.gov/pubmed/24997640 http://dx.doi.org/10.1186/1746-1596-9-137 |
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