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Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma

PURPOSE: Colon adenocarcinoma (COAD) is the third most common malignancy globally and is further categorized as left colon adenocarcinoma (LCOAD) or right colon adenocarcinoma (RCOAD) depending on the location of the primary tumor. The therapeutic outcome and long-term prognosis for patients with CO...

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Autores principales: Han, Jing, Zhang, Xue, Yang, Yang, Feng, Li, Wang, Gui-Ying, Zhang, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201700/
https://www.ncbi.nlm.nih.gov/pubmed/32420374
http://dx.doi.org/10.1155/2020/8465068
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author Han, Jing
Zhang, Xue
Yang, Yang
Feng, Li
Wang, Gui-Ying
Zhang, Nan
author_facet Han, Jing
Zhang, Xue
Yang, Yang
Feng, Li
Wang, Gui-Ying
Zhang, Nan
author_sort Han, Jing
collection PubMed
description PURPOSE: Colon adenocarcinoma (COAD) is the third most common malignancy globally and is further categorized as left colon adenocarcinoma (LCOAD) or right colon adenocarcinoma (RCOAD) depending on the location of the primary tumor. The therapeutic outcome and long-term prognosis for patients with COAD are less than satisfactory, and this may be associated with tumor location. Therefore, it is important to investigate the genetic differences in COAD at different sites. Patients and Methods. Public data associated with COAD were downloaded from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were identified using R software (version 3.5.3), and functional annotation of DEGs was performed using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. A protein-protein interaction network was constructed, hub genes were identified and analyzed, and data mining using Gene Expression Profiling Interactive Analysis (GEPIA) was conducted. RESULTS: A total of 286 DEGs were identified between LCOAD and RCOAD. Additionally, 10 hub genes associated with COAD at different locations were screened, namely, CDKN2A, IGF1R, MDM2, SMAD3, SLC2A1, GRM5, PLCB4, FGFR1, UBE2V2, and TNFRSF10B. The expression of cyclin-dependent kinase inhibitor 2A (CDKN2A) and solute carrier family 2 member 1 (SLC2A1) was significantly associated with pathological stage (P < 0.05). COAD patients with high expression levels of CDKN2A exhibited poorer overall survival (OS) times than those with low expression levels (P < 0.05). CONCLUSION: CDKN2A expression was significantly different between LCOAD and RCOAD and was closely related to the prognosis of COAD. It is of great value for further understanding of the pathogenesis of LCOAD and RCOAD.
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spelling pubmed-72017002020-05-15 Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma Han, Jing Zhang, Xue Yang, Yang Feng, Li Wang, Gui-Ying Zhang, Nan Biomed Res Int Research Article PURPOSE: Colon adenocarcinoma (COAD) is the third most common malignancy globally and is further categorized as left colon adenocarcinoma (LCOAD) or right colon adenocarcinoma (RCOAD) depending on the location of the primary tumor. The therapeutic outcome and long-term prognosis for patients with COAD are less than satisfactory, and this may be associated with tumor location. Therefore, it is important to investigate the genetic differences in COAD at different sites. Patients and Methods. Public data associated with COAD were downloaded from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were identified using R software (version 3.5.3), and functional annotation of DEGs was performed using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. A protein-protein interaction network was constructed, hub genes were identified and analyzed, and data mining using Gene Expression Profiling Interactive Analysis (GEPIA) was conducted. RESULTS: A total of 286 DEGs were identified between LCOAD and RCOAD. Additionally, 10 hub genes associated with COAD at different locations were screened, namely, CDKN2A, IGF1R, MDM2, SMAD3, SLC2A1, GRM5, PLCB4, FGFR1, UBE2V2, and TNFRSF10B. The expression of cyclin-dependent kinase inhibitor 2A (CDKN2A) and solute carrier family 2 member 1 (SLC2A1) was significantly associated with pathological stage (P < 0.05). COAD patients with high expression levels of CDKN2A exhibited poorer overall survival (OS) times than those with low expression levels (P < 0.05). CONCLUSION: CDKN2A expression was significantly different between LCOAD and RCOAD and was closely related to the prognosis of COAD. It is of great value for further understanding of the pathogenesis of LCOAD and RCOAD. Hindawi 2020-01-21 /pmc/articles/PMC7201700/ /pubmed/32420374 http://dx.doi.org/10.1155/2020/8465068 Text en Copyright © 2020 Jing Han et al. http://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
Han, Jing
Zhang, Xue
Yang, Yang
Feng, Li
Wang, Gui-Ying
Zhang, Nan
Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title_full Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title_fullStr Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title_full_unstemmed Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title_short Screening and Identification of Differentially Expressed Genes Expressed among Left and Right Colon Adenocarcinoma
title_sort screening and identification of differentially expressed genes expressed among left and right colon adenocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201700/
https://www.ncbi.nlm.nih.gov/pubmed/32420374
http://dx.doi.org/10.1155/2020/8465068
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