Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.

Integrated analysis of genomic and transcriptomic level changes holds promise for a better understanding of colorectal cancer (CRC) biology. There is a pertinent need to explain the functional effect of genome level changes by integrating the information at the transcript level. Using high resolutio...

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Autores principales: Mohammad Azhar Aziz, Sathish Periyasamy, Zeyad Al Yousef, Ibrahim AlAbdulkarim, Majed Al Otaibi, Abdulaziz Alfahed, Glowi Alasiri
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/cc13a20360bc41bbb0446401f3b178a2
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spelling oai:doaj.org-article:cc13a20360bc41bbb0446401f3b178a22021-11-25T05:55:39ZIntegrated exon level expression analysis of driver genes explain their role in colorectal cancer.1932-620310.1371/journal.pone.0110134https://doaj.org/article/cc13a20360bc41bbb0446401f3b178a22014-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0110134https://doaj.org/toc/1932-6203Integrated analysis of genomic and transcriptomic level changes holds promise for a better understanding of colorectal cancer (CRC) biology. There is a pertinent need to explain the functional effect of genome level changes by integrating the information at the transcript level. Using high resolution cytogenetics array, we had earlier identified driver genes by 'Genomic Identification of Significant Targets In Cancer (GISTIC)' analysis of paired tumour-normal samples from colorectal cancer patients. In this study, we analyze these driver genes at three levels using exon array data--gene, exon and network. Gene level analysis revealed a small subset to experience differential expression. These results were reinforced by carrying out separate differential expression analyses (SAM and LIMMA). ATP8B1 was found to be the novel gene associated with CRC that shows changes at cytogenetic, gene and exon levels. Splice index of 29 exons corresponding to 13 genes was found to be significantly altered in tumour samples. Driver genes were used to construct regulatory networks for tumour and normal groups. There were rearrangements in transcription factor genes suggesting the presence of regulatory switching. The regulatory pattern of AHR gene was found to have the most significant alteration. Our results integrate data with focus on driver genes resulting in highly enriched novel molecules that need further studies to establish their role in CRC.Mohammad Azhar AzizSathish PeriyasamyZeyad Al YousefIbrahim AlAbdulkarimMajed Al OtaibiAbdulaziz AlfahedGlowi AlasiriPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 10, p e110134 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mohammad Azhar Aziz
Sathish Periyasamy
Zeyad Al Yousef
Ibrahim AlAbdulkarim
Majed Al Otaibi
Abdulaziz Alfahed
Glowi Alasiri
Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
description Integrated analysis of genomic and transcriptomic level changes holds promise for a better understanding of colorectal cancer (CRC) biology. There is a pertinent need to explain the functional effect of genome level changes by integrating the information at the transcript level. Using high resolution cytogenetics array, we had earlier identified driver genes by 'Genomic Identification of Significant Targets In Cancer (GISTIC)' analysis of paired tumour-normal samples from colorectal cancer patients. In this study, we analyze these driver genes at three levels using exon array data--gene, exon and network. Gene level analysis revealed a small subset to experience differential expression. These results were reinforced by carrying out separate differential expression analyses (SAM and LIMMA). ATP8B1 was found to be the novel gene associated with CRC that shows changes at cytogenetic, gene and exon levels. Splice index of 29 exons corresponding to 13 genes was found to be significantly altered in tumour samples. Driver genes were used to construct regulatory networks for tumour and normal groups. There were rearrangements in transcription factor genes suggesting the presence of regulatory switching. The regulatory pattern of AHR gene was found to have the most significant alteration. Our results integrate data with focus on driver genes resulting in highly enriched novel molecules that need further studies to establish their role in CRC.
format article
author Mohammad Azhar Aziz
Sathish Periyasamy
Zeyad Al Yousef
Ibrahim AlAbdulkarim
Majed Al Otaibi
Abdulaziz Alfahed
Glowi Alasiri
author_facet Mohammad Azhar Aziz
Sathish Periyasamy
Zeyad Al Yousef
Ibrahim AlAbdulkarim
Majed Al Otaibi
Abdulaziz Alfahed
Glowi Alasiri
author_sort Mohammad Azhar Aziz
title Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
title_short Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
title_full Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
title_fullStr Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
title_full_unstemmed Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
title_sort integrated exon level expression analysis of driver genes explain their role in colorectal cancer.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/cc13a20360bc41bbb0446401f3b178a2
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AT sathishperiyasamy integratedexonlevelexpressionanalysisofdrivergenesexplaintheirroleincolorectalcancer
AT zeyadalyousef integratedexonlevelexpressionanalysisofdrivergenesexplaintheirroleincolorectalcancer
AT ibrahimalabdulkarim integratedexonlevelexpressionanalysisofdrivergenesexplaintheirroleincolorectalcancer
AT majedalotaibi integratedexonlevelexpressionanalysisofdrivergenesexplaintheirroleincolorectalcancer
AT abdulazizalfahed integratedexonlevelexpressionanalysisofdrivergenesexplaintheirroleincolorectalcancer
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