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Transcriptomic analysis of esophageal cancer reveals hub genes and networks involved in cancer progression
Esophageal carcinoma (ESCA) has a 5-year survival rate of fewer than 20%. The study aimed to identify new predictive biomarkers for ESCA through transcriptomics meta-analysis to address the problems of ineffective cancer therapy, lack of efficient diagnostic tools, and costly screening and contribut...
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Published in: | Computers in biology and medicine 2023-06, Vol.159, p.106944-106944, Article 106944 |
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description | Esophageal carcinoma (ESCA) has a 5-year survival rate of fewer than 20%. The study aimed to identify new predictive biomarkers for ESCA through transcriptomics meta-analysis to address the problems of ineffective cancer therapy, lack of efficient diagnostic tools, and costly screening and contribute to developing more efficient cancer screening and treatments by identifying new marker genes. Nine GEO datasets of three kinds of esophageal carcinoma were analyzed, and 20 differentially expressed genes were detected in carcinogenic pathways. Network analysis revealed four hub genes, namely RAR Related Orphan Receptor A (RORA), lysine acetyltransferase 2B (KAT2B), Cell Division Cycle 25B (CDC25B), and Epithelial Cell Transforming 2 (ECT2). Overexpression of RORA, KAT2B, and ECT2 was identified with a bad prognosis. These hub genes modulate immune cell infiltration. These hub genes modulate immune cell infiltration. Although this research needs lab confirmation, we found interesting biomarkers in ESCA that may aid in diagnosis and treatment.
•The study was conducted using computational analysis to learn more about the molecular mechanism of esophageal cancer.•A wide range of datasets, including both Microarray and RNAseq, was considered to discover potential biomarkers.•Following extensive analysis, 4 hub genes were discovered that can be studied for the proper therapeutic measure.•Involvement of the hub genes with other cancer types and their regulatory networks were observed.•This research will help determine how common medical conditions affect health and develop esophageal cancer. |
doi_str_mv | 10.1016/j.compbiomed.2023.106944 |
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•The study was conducted using computational analysis to learn more about the molecular mechanism of esophageal cancer.•A wide range of datasets, including both Microarray and RNAseq, was considered to discover potential biomarkers.•Following extensive analysis, 4 hub genes were discovered that can be studied for the proper therapeutic measure.•Involvement of the hub genes with other cancer types and their regulatory networks were observed.•This research will help determine how common medical conditions affect health and develop esophageal cancer.</description><identifier>ISSN: 0010-4825</identifier><identifier>EISSN: 1879-0534</identifier><identifier>DOI: 10.1016/j.compbiomed.2023.106944</identifier><identifier>PMID: 37075603</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Acetyltransferase ; Algorithms ; Biomarkers ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cancer ; Cancer screening ; Cancer therapies ; Carcinogens ; Cdc25B phosphatase ; Cell division ; Computational Biology ; Datasets ; Differentially expressed genes ; Epithelial cells ; Epithelium ; Esophageal cancer ; Esophageal carcinoma ; Esophageal Neoplasms - genetics ; Esophagus ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Gene ontology ; Gene Regulatory Networks ; Genes ; Genomes ; Hub genes ; Humans ; Immune system ; Infiltration ; Lysine ; Medical prognosis ; Network analysis ; Ontology ; Open source software ; Protein Interaction Maps - genetics ; Protein-protein interaction ; Proteins ; Sample size ; Screening ; Surgery ; Survival ; Survival analysis ; Transcriptome - genetics ; Transcriptomics</subject><ispartof>Computers in biology and medicine, 2023-06, Vol.159, p.106944-106944, Article 106944</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. All rights reserved.</rights><rights>2023. Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-4aae5f48e906b808472b9a42a83f2e4fc4656880d97714f8c2a3ed74b32c6e673</citedby><cites>FETCH-LOGICAL-c402t-4aae5f48e906b808472b9a42a83f2e4fc4656880d97714f8c2a3ed74b32c6e673</cites><orcidid>0000-0001-8882-6381 ; 0000-0002-9637-4343 ; 0000-0001-6969-6788</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37075603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chatterjee, Dipankor</creatorcontrib><creatorcontrib>Rahman, Md Mostafijur</creatorcontrib><creatorcontrib>Saha, Anik Kumar</creatorcontrib><creatorcontrib>Siam, Mohammad Kawsar Sharif</creatorcontrib><creatorcontrib>Sharif Shohan, Mohammad Umer</creatorcontrib><title>Transcriptomic analysis of esophageal cancer reveals hub genes and networks involved in cancer progression</title><title>Computers in biology and medicine</title><addtitle>Comput Biol Med</addtitle><description>Esophageal carcinoma (ESCA) has a 5-year survival rate of fewer than 20%. The study aimed to identify new predictive biomarkers for ESCA through transcriptomics meta-analysis to address the problems of ineffective cancer therapy, lack of efficient diagnostic tools, and costly screening and contribute to developing more efficient cancer screening and treatments by identifying new marker genes. Nine GEO datasets of three kinds of esophageal carcinoma were analyzed, and 20 differentially expressed genes were detected in carcinogenic pathways. Network analysis revealed four hub genes, namely RAR Related Orphan Receptor A (RORA), lysine acetyltransferase 2B (KAT2B), Cell Division Cycle 25B (CDC25B), and Epithelial Cell Transforming 2 (ECT2). Overexpression of RORA, KAT2B, and ECT2 was identified with a bad prognosis. These hub genes modulate immune cell infiltration. These hub genes modulate immune cell infiltration. Although this research needs lab confirmation, we found interesting biomarkers in ESCA that may aid in diagnosis and treatment.
•The study was conducted using computational analysis to learn more about the molecular mechanism of esophageal cancer.•A wide range of datasets, including both Microarray and RNAseq, was considered to discover potential biomarkers.•Following extensive analysis, 4 hub genes were discovered that can be studied for the proper therapeutic measure.•Involvement of the hub genes with other cancer types and their regulatory networks were observed.•This research will help determine how common medical conditions affect health and develop esophageal cancer.</description><subject>Acetyltransferase</subject><subject>Algorithms</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>Cancer screening</subject><subject>Cancer therapies</subject><subject>Carcinogens</subject><subject>Cdc25B phosphatase</subject><subject>Cell division</subject><subject>Computational Biology</subject><subject>Datasets</subject><subject>Differentially expressed genes</subject><subject>Epithelial cells</subject><subject>Epithelium</subject><subject>Esophageal cancer</subject><subject>Esophageal carcinoma</subject><subject>Esophageal Neoplasms - genetics</subject><subject>Esophagus</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene ontology</subject><subject>Gene Regulatory Networks</subject><subject>Genes</subject><subject>Genomes</subject><subject>Hub genes</subject><subject>Humans</subject><subject>Immune system</subject><subject>Infiltration</subject><subject>Lysine</subject><subject>Medical prognosis</subject><subject>Network analysis</subject><subject>Ontology</subject><subject>Open source software</subject><subject>Protein Interaction Maps - genetics</subject><subject>Protein-protein interaction</subject><subject>Proteins</subject><subject>Sample size</subject><subject>Screening</subject><subject>Surgery</subject><subject>Survival</subject><subject>Survival analysis</subject><subject>Transcriptome - genetics</subject><subject>Transcriptomics</subject><issn>0010-4825</issn><issn>1879-0534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS0EokvhKyBLXLhkmdiO4xyhKn-kSlzK2XKcydYhiYMnWdRvj1fbFRIXTh57fs9Peo8xXsK-hFJ_GPY-Tksb4oTdXoCQ-Vk3Sj1ju9LUTQGVVM_ZDqCEQhlRXbFXRAMAKJDwkl3JGupKg9yx4T65mXwKyxqn4Lmb3fhIgXjsOVJcHtwB3ci9mz0mnvCYb8QftpYfcEbKfMdnXH_H9JN4mI9xPGKXh4tiSfGQkCjE-TV70Wcxvnk6r9mPz7f3N1-Lu-9fvt18vCu8ArEWyjmsemWwAd0aMKoWbeOUcEb2AlXvla60MdA1dV2q3njhJHa1aqXwGnUtr9n787_Z-9eGtNopkMdxdDPGjawwIButjdYZffcPOsQt5QhOVE66UjnXTJkz5VMkStjbJYXJpUdbgj31YQf7tw976sOe-8jSt08GW3vaXYSXAjLw6QxgTuQYMFnyAXN0XUjoV9vF8H-XP5-Lodg</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Chatterjee, Dipankor</creator><creator>Rahman, Md Mostafijur</creator><creator>Saha, Anik Kumar</creator><creator>Siam, Mohammad Kawsar Sharif</creator><creator>Sharif Shohan, Mohammad Umer</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AL</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0N</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>M7Z</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8882-6381</orcidid><orcidid>https://orcid.org/0000-0002-9637-4343</orcidid><orcidid>https://orcid.org/0000-0001-6969-6788</orcidid></search><sort><creationdate>202306</creationdate><title>Transcriptomic analysis of esophageal cancer reveals hub genes and networks involved in cancer progression</title><author>Chatterjee, Dipankor ; Rahman, Md Mostafijur ; Saha, Anik Kumar ; Siam, Mohammad Kawsar Sharif ; Sharif Shohan, Mohammad Umer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-4aae5f48e906b808472b9a42a83f2e4fc4656880d97714f8c2a3ed74b32c6e673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetyltransferase</topic><topic>Algorithms</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer</topic><topic>Cancer screening</topic><topic>Cancer therapies</topic><topic>Carcinogens</topic><topic>Cdc25B phosphatase</topic><topic>Cell division</topic><topic>Computational Biology</topic><topic>Datasets</topic><topic>Differentially expressed genes</topic><topic>Epithelial cells</topic><topic>Epithelium</topic><topic>Esophageal cancer</topic><topic>Esophageal carcinoma</topic><topic>Esophageal Neoplasms - genetics</topic><topic>Esophagus</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene ontology</topic><topic>Gene Regulatory Networks</topic><topic>Genes</topic><topic>Genomes</topic><topic>Hub genes</topic><topic>Humans</topic><topic>Immune system</topic><topic>Infiltration</topic><topic>Lysine</topic><topic>Medical prognosis</topic><topic>Network analysis</topic><topic>Ontology</topic><topic>Open source software</topic><topic>Protein Interaction Maps - genetics</topic><topic>Protein-protein interaction</topic><topic>Proteins</topic><topic>Sample size</topic><topic>Screening</topic><topic>Surgery</topic><topic>Survival</topic><topic>Survival analysis</topic><topic>Transcriptome - genetics</topic><topic>Transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chatterjee, Dipankor</creatorcontrib><creatorcontrib>Rahman, Md Mostafijur</creatorcontrib><creatorcontrib>Saha, Anik Kumar</creatorcontrib><creatorcontrib>Siam, Mohammad Kawsar Sharif</creatorcontrib><creatorcontrib>Sharif Shohan, Mohammad Umer</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Computing Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Computing Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Computers in biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chatterjee, Dipankor</au><au>Rahman, Md Mostafijur</au><au>Saha, Anik Kumar</au><au>Siam, Mohammad Kawsar Sharif</au><au>Sharif Shohan, Mohammad Umer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptomic analysis of esophageal cancer reveals hub genes and networks involved in cancer progression</atitle><jtitle>Computers in biology and medicine</jtitle><addtitle>Comput Biol Med</addtitle><date>2023-06</date><risdate>2023</risdate><volume>159</volume><spage>106944</spage><epage>106944</epage><pages>106944-106944</pages><artnum>106944</artnum><issn>0010-4825</issn><eissn>1879-0534</eissn><abstract>Esophageal carcinoma (ESCA) has a 5-year survival rate of fewer than 20%. The study aimed to identify new predictive biomarkers for ESCA through transcriptomics meta-analysis to address the problems of ineffective cancer therapy, lack of efficient diagnostic tools, and costly screening and contribute to developing more efficient cancer screening and treatments by identifying new marker genes. Nine GEO datasets of three kinds of esophageal carcinoma were analyzed, and 20 differentially expressed genes were detected in carcinogenic pathways. Network analysis revealed four hub genes, namely RAR Related Orphan Receptor A (RORA), lysine acetyltransferase 2B (KAT2B), Cell Division Cycle 25B (CDC25B), and Epithelial Cell Transforming 2 (ECT2). Overexpression of RORA, KAT2B, and ECT2 was identified with a bad prognosis. These hub genes modulate immune cell infiltration. These hub genes modulate immune cell infiltration. Although this research needs lab confirmation, we found interesting biomarkers in ESCA that may aid in diagnosis and treatment.
•The study was conducted using computational analysis to learn more about the molecular mechanism of esophageal cancer.•A wide range of datasets, including both Microarray and RNAseq, was considered to discover potential biomarkers.•Following extensive analysis, 4 hub genes were discovered that can be studied for the proper therapeutic measure.•Involvement of the hub genes with other cancer types and their regulatory networks were observed.•This research will help determine how common medical conditions affect health and develop esophageal cancer.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>37075603</pmid><doi>10.1016/j.compbiomed.2023.106944</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8882-6381</orcidid><orcidid>https://orcid.org/0000-0002-9637-4343</orcidid><orcidid>https://orcid.org/0000-0001-6969-6788</orcidid></addata></record> |
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subjects | Acetyltransferase Algorithms Biomarkers Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Cancer Cancer screening Cancer therapies Carcinogens Cdc25B phosphatase Cell division Computational Biology Datasets Differentially expressed genes Epithelial cells Epithelium Esophageal cancer Esophageal carcinoma Esophageal Neoplasms - genetics Esophagus Gene expression Gene Expression Profiling Gene Expression Regulation, Neoplastic Gene ontology Gene Regulatory Networks Genes Genomes Hub genes Humans Immune system Infiltration Lysine Medical prognosis Network analysis Ontology Open source software Protein Interaction Maps - genetics Protein-protein interaction Proteins Sample size Screening Surgery Survival Survival analysis Transcriptome - genetics Transcriptomics |
title | Transcriptomic analysis of esophageal cancer reveals hub genes and networks involved in cancer progression |
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