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Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis
Lung cancer is the primary and third most frequently detected form of cancer in both males and females. The present study tries to perform integrated analysis in male as well as female patients inclusively both smoker and non-smokers. This study aims to identify diagnostic biomarkers and therapeutic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625372/ https://www.ncbi.nlm.nih.gov/pubmed/37928493 http://dx.doi.org/10.6026/97320630019954 |
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author | Hayat, Shaheen Ishrat, Romana |
author_facet | Hayat, Shaheen Ishrat, Romana |
author_sort | Hayat, Shaheen |
collection | PubMed |
description | Lung cancer is the primary and third most frequently detected form of cancer in both males and females. The present study tries to perform integrated analysis in male as well as female patients inclusively both smoker and non-smokers. This study aims to identify diagnostic biomarkers and therapeutic targets for lung cancer patients using human microarray profile datasets. Differentially expressed genes (DEGs) were identified using a PPI network from the String database, and major modules or clusters were extracted using MCODE. The Cytohubba plug-in was used to find hub genes from the PPI network using centralities approaches. Twenty significant hub genes (CCND1, CDK1, CCNB1, CDH1, TP53, CTNNB1, EGFR, ESR1, CDK2, CCNA2, RHOA, EGF, FN1, HSP90AA1, STAT3, JUN, NOTCH1, IL6, SRC, and CD44) were identified as promising diagnostic biomarkers and therapeutic targets for lung cancer treatment. Survival analysis and hub gene validation were also conducted. GO enrichment and pathway analysis were conducted to identify their important functions. These hub genes were also used to identify targeted drugs. The findings suggest that the identified genes have the potential to be used as diagnostic biomarkers and therapeutic targets for lung cancer treatment. |
format | Online Article Text |
id | pubmed-10625372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-106253722023-11-05 Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis Hayat, Shaheen Ishrat, Romana Bioinformation Research Article Lung cancer is the primary and third most frequently detected form of cancer in both males and females. The present study tries to perform integrated analysis in male as well as female patients inclusively both smoker and non-smokers. This study aims to identify diagnostic biomarkers and therapeutic targets for lung cancer patients using human microarray profile datasets. Differentially expressed genes (DEGs) were identified using a PPI network from the String database, and major modules or clusters were extracted using MCODE. The Cytohubba plug-in was used to find hub genes from the PPI network using centralities approaches. Twenty significant hub genes (CCND1, CDK1, CCNB1, CDH1, TP53, CTNNB1, EGFR, ESR1, CDK2, CCNA2, RHOA, EGF, FN1, HSP90AA1, STAT3, JUN, NOTCH1, IL6, SRC, and CD44) were identified as promising diagnostic biomarkers and therapeutic targets for lung cancer treatment. Survival analysis and hub gene validation were also conducted. GO enrichment and pathway analysis were conducted to identify their important functions. These hub genes were also used to identify targeted drugs. The findings suggest that the identified genes have the potential to be used as diagnostic biomarkers and therapeutic targets for lung cancer treatment. Biomedical Informatics 2023-09-30 /pmc/articles/PMC10625372/ /pubmed/37928493 http://dx.doi.org/10.6026/97320630019954 Text en © 2023 Biomedical Informatics https://creativecommons.org/licenses/by/3.0/This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Research Article Hayat, Shaheen Ishrat, Romana Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title | Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title_full | Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title_fullStr | Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title_full_unstemmed | Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title_short | Exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
title_sort | exploring potential genes and pathways related to lung cancer: a graph theoretical analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625372/ https://www.ncbi.nlm.nih.gov/pubmed/37928493 http://dx.doi.org/10.6026/97320630019954 |
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