Machine learning analysis of CD4+ T cell gene expression in diverse diseases: insights from cancer, metabolic, respiratory, and digestive disorders
•CD4+ T cells exhibit different immune responses to different diseases.•The expression profile data of CD4+ T cells on various diseases was deeply analyzed.•Special expression patterns were discovered for different diseases. CD4+ T cells play a pivotal role in the immune system, particularly in adap...
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Veröffentlicht in: | Cancer genetics 2025-01, Vol.290-291, p.56-60 |
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container_title | Cancer genetics |
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creator | Liao, HuiPing Ma, QingLan Chen, Lei Guo, Wei Feng, KaiYan Bao, YuSheng Zhang, Yu Shen, WenFeng Huang, Tao Cai, Yu-Dong |
description | •CD4+ T cells exhibit different immune responses to different diseases.•The expression profile data of CD4+ T cells on various diseases was deeply analyzed.•Special expression patterns were discovered for different diseases.
CD4+ T cells play a pivotal role in the immune system, particularly in adaptive immunity, by orchestrating and enhancing immune responses. CD4+ T cell-related immune responses exhibit diverse characteristics in different diseases. This study utilizes gene expression analysis of CD4+ T cells to classify and understand complex diseases. We analyzed the dataset consisting of samples from various diseases, including cancers, metabolic disorders, circulatory and respiratory diseases, and digestive ailments, as well as 53 healthy controls. Each sample contained expression data for 22,881 genes. Four feature ranking algorithms, incremental feature selection method, synthetic minority oversampling technique, and four classification algorithms were utilized to pinpoint essential genes, extract classification rules and build efficient classifiers. The following analysis focused on genes across rules, such as AK4, CALU, LINC01271, and RUSC1-AS1. AK4 and CALU show fluctuating levels in diseases like asthma, Crohn's disease, and breast cancer. The analysis results and existing research suggest that they may play a role in these diseases. LINC01271 generally has higher expression in conditions including asthma, Crohn's disease, and diabetes. RUSC1-AS1 is more expressed in chronic diseases like asthma and Crohn's, but less in acute illnesses like tonsillitis and influenza. This highlights the distinct roles of these genes in different diseases. Our approach highlights the potential for developing novel therapeutic strategies based on the transcriptional profiles of CD4+ T cells. |
doi_str_mv | 10.1016/j.cancergen.2024.12.004 |
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CD4+ T cells play a pivotal role in the immune system, particularly in adaptive immunity, by orchestrating and enhancing immune responses. CD4+ T cell-related immune responses exhibit diverse characteristics in different diseases. This study utilizes gene expression analysis of CD4+ T cells to classify and understand complex diseases. We analyzed the dataset consisting of samples from various diseases, including cancers, metabolic disorders, circulatory and respiratory diseases, and digestive ailments, as well as 53 healthy controls. Each sample contained expression data for 22,881 genes. Four feature ranking algorithms, incremental feature selection method, synthetic minority oversampling technique, and four classification algorithms were utilized to pinpoint essential genes, extract classification rules and build efficient classifiers. The following analysis focused on genes across rules, such as AK4, CALU, LINC01271, and RUSC1-AS1. AK4 and CALU show fluctuating levels in diseases like asthma, Crohn's disease, and breast cancer. The analysis results and existing research suggest that they may play a role in these diseases. LINC01271 generally has higher expression in conditions including asthma, Crohn's disease, and diabetes. RUSC1-AS1 is more expressed in chronic diseases like asthma and Crohn's, but less in acute illnesses like tonsillitis and influenza. This highlights the distinct roles of these genes in different diseases. Our approach highlights the potential for developing novel therapeutic strategies based on the transcriptional profiles of CD4+ T cells.</description><identifier>ISSN: 2210-7762</identifier><identifier>DOI: 10.1016/j.cancergen.2024.12.004</identifier><identifier>PMID: 39729927</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>CD4+ T cell ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - metabolism ; Complex disease ; Digestive System Diseases - genetics ; Digestive System Diseases - immunology ; Feature selection ; Gene Expression Profiling ; Humans ; Machine Learning ; Metabolic Diseases - genetics ; Metabolic Diseases - immunology ; Neoplasms - genetics ; Neoplasms - immunology ; Respiration Disorders - genetics ; Respiration Disorders - immunology ; Respiratory Tract Diseases - genetics ; Respiratory Tract Diseases - immunology</subject><ispartof>Cancer genetics, 2025-01, Vol.290-291, p.56-60</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c247t-ff1ef02db4aa8d70e73a008777e53508358bd00ac3535b6bfe0504472f8d9b7e3</cites><orcidid>0000-0001-5664-7979</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2210776224001571$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39729927$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liao, HuiPing</creatorcontrib><creatorcontrib>Ma, QingLan</creatorcontrib><creatorcontrib>Chen, Lei</creatorcontrib><creatorcontrib>Guo, Wei</creatorcontrib><creatorcontrib>Feng, KaiYan</creatorcontrib><creatorcontrib>Bao, YuSheng</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Shen, WenFeng</creatorcontrib><creatorcontrib>Huang, Tao</creatorcontrib><creatorcontrib>Cai, Yu-Dong</creatorcontrib><title>Machine learning analysis of CD4+ T cell gene expression in diverse diseases: insights from cancer, metabolic, respiratory, and digestive disorders</title><title>Cancer genetics</title><addtitle>Cancer Genet</addtitle><description>•CD4+ T cells exhibit different immune responses to different diseases.•The expression profile data of CD4+ T cells on various diseases was deeply analyzed.•Special expression patterns were discovered for different diseases.
CD4+ T cells play a pivotal role in the immune system, particularly in adaptive immunity, by orchestrating and enhancing immune responses. CD4+ T cell-related immune responses exhibit diverse characteristics in different diseases. This study utilizes gene expression analysis of CD4+ T cells to classify and understand complex diseases. We analyzed the dataset consisting of samples from various diseases, including cancers, metabolic disorders, circulatory and respiratory diseases, and digestive ailments, as well as 53 healthy controls. Each sample contained expression data for 22,881 genes. Four feature ranking algorithms, incremental feature selection method, synthetic minority oversampling technique, and four classification algorithms were utilized to pinpoint essential genes, extract classification rules and build efficient classifiers. The following analysis focused on genes across rules, such as AK4, CALU, LINC01271, and RUSC1-AS1. AK4 and CALU show fluctuating levels in diseases like asthma, Crohn's disease, and breast cancer. The analysis results and existing research suggest that they may play a role in these diseases. LINC01271 generally has higher expression in conditions including asthma, Crohn's disease, and diabetes. RUSC1-AS1 is more expressed in chronic diseases like asthma and Crohn's, but less in acute illnesses like tonsillitis and influenza. This highlights the distinct roles of these genes in different diseases. Our approach highlights the potential for developing novel therapeutic strategies based on the transcriptional profiles of CD4+ T cells.</description><subject>CD4+ T cell</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>Complex disease</subject><subject>Digestive System Diseases - genetics</subject><subject>Digestive System Diseases - immunology</subject><subject>Feature selection</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Machine Learning</subject><subject>Metabolic Diseases - genetics</subject><subject>Metabolic Diseases - immunology</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - immunology</subject><subject>Respiration Disorders - genetics</subject><subject>Respiration Disorders - immunology</subject><subject>Respiratory Tract Diseases - genetics</subject><subject>Respiratory Tract Diseases - immunology</subject><issn>2210-7762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUctuGyEUZZGqidL8QssyUu0pMIyZ6S5y-pJSdZOuEQN3HKwZcLnjKP6O_HCv5TTbsrkCncc9HMY-SFFJIVeftpV3yUPZQKqUULqSqhJCn7ELpaRYGrNS5-wKcSvo6Ea0pn7LzuvOqK5T5oI9_3T-ISbgI7iSYtpwl9x4wIg8D3x9qz_ye-5hHDk5AIenXQHEmBOPiYf4CAWBJoJDwM_0iHHzMCMfSp74abUFn2B2fR6jX3Bi72Jxcy6HBVkF4m4AZxI6quQSSPAdezO4EeHqZV6y31-_3K-_L-9-ffuxvrlbeqXNvBwGCYNQodfOtcEIMLUTFNAYaGpKWjdtH4RwvqZrv-oHEI3Q2qihDV1voL5k1yfdXcl_9rSFnSIes7oEeY-2lrozzaptBUHNCepLRiww2F2JkysHK4U9FmG39rUIeyzCSmXpx4n5_sVk308QXnn_KiDAzQkAFPUxQrHoI5BUiAX8bEOO_zX5Czfbocw</recordid><startdate>202501</startdate><enddate>202501</enddate><creator>Liao, HuiPing</creator><creator>Ma, QingLan</creator><creator>Chen, Lei</creator><creator>Guo, Wei</creator><creator>Feng, KaiYan</creator><creator>Bao, YuSheng</creator><creator>Zhang, Yu</creator><creator>Shen, WenFeng</creator><creator>Huang, Tao</creator><creator>Cai, Yu-Dong</creator><general>Elsevier Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0001-5664-7979</orcidid></search><sort><creationdate>202501</creationdate><title>Machine learning analysis of CD4+ T cell gene expression in diverse diseases: insights from cancer, metabolic, respiratory, and digestive disorders</title><author>Liao, HuiPing ; Ma, QingLan ; Chen, Lei ; Guo, Wei ; Feng, KaiYan ; Bao, YuSheng ; Zhang, Yu ; Shen, WenFeng ; Huang, Tao ; Cai, Yu-Dong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c247t-ff1ef02db4aa8d70e73a008777e53508358bd00ac3535b6bfe0504472f8d9b7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>CD4+ T cell</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>Complex disease</topic><topic>Digestive System Diseases - genetics</topic><topic>Digestive System Diseases - immunology</topic><topic>Feature selection</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Machine Learning</topic><topic>Metabolic Diseases - genetics</topic><topic>Metabolic Diseases - immunology</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - immunology</topic><topic>Respiration Disorders - genetics</topic><topic>Respiration Disorders - immunology</topic><topic>Respiratory Tract Diseases - genetics</topic><topic>Respiratory Tract Diseases - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liao, HuiPing</creatorcontrib><creatorcontrib>Ma, QingLan</creatorcontrib><creatorcontrib>Chen, Lei</creatorcontrib><creatorcontrib>Guo, Wei</creatorcontrib><creatorcontrib>Feng, KaiYan</creatorcontrib><creatorcontrib>Bao, YuSheng</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Shen, WenFeng</creatorcontrib><creatorcontrib>Huang, Tao</creatorcontrib><creatorcontrib>Cai, Yu-Dong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liao, HuiPing</au><au>Ma, QingLan</au><au>Chen, Lei</au><au>Guo, Wei</au><au>Feng, KaiYan</au><au>Bao, YuSheng</au><au>Zhang, Yu</au><au>Shen, WenFeng</au><au>Huang, Tao</au><au>Cai, Yu-Dong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Machine learning analysis of CD4+ T cell gene expression in diverse diseases: insights from cancer, metabolic, respiratory, and digestive disorders</atitle><jtitle>Cancer genetics</jtitle><addtitle>Cancer Genet</addtitle><date>2025-01</date><risdate>2025</risdate><volume>290-291</volume><spage>56</spage><epage>60</epage><pages>56-60</pages><issn>2210-7762</issn><abstract>•CD4+ T cells exhibit different immune responses to different diseases.•The expression profile data of CD4+ T cells on various diseases was deeply analyzed.•Special expression patterns were discovered for different diseases.
CD4+ T cells play a pivotal role in the immune system, particularly in adaptive immunity, by orchestrating and enhancing immune responses. CD4+ T cell-related immune responses exhibit diverse characteristics in different diseases. This study utilizes gene expression analysis of CD4+ T cells to classify and understand complex diseases. We analyzed the dataset consisting of samples from various diseases, including cancers, metabolic disorders, circulatory and respiratory diseases, and digestive ailments, as well as 53 healthy controls. Each sample contained expression data for 22,881 genes. Four feature ranking algorithms, incremental feature selection method, synthetic minority oversampling technique, and four classification algorithms were utilized to pinpoint essential genes, extract classification rules and build efficient classifiers. The following analysis focused on genes across rules, such as AK4, CALU, LINC01271, and RUSC1-AS1. AK4 and CALU show fluctuating levels in diseases like asthma, Crohn's disease, and breast cancer. The analysis results and existing research suggest that they may play a role in these diseases. LINC01271 generally has higher expression in conditions including asthma, Crohn's disease, and diabetes. RUSC1-AS1 is more expressed in chronic diseases like asthma and Crohn's, but less in acute illnesses like tonsillitis and influenza. This highlights the distinct roles of these genes in different diseases. Our approach highlights the potential for developing novel therapeutic strategies based on the transcriptional profiles of CD4+ T cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39729927</pmid><doi>10.1016/j.cancergen.2024.12.004</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-5664-7979</orcidid></addata></record> |
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subjects | CD4+ T cell CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - metabolism Complex disease Digestive System Diseases - genetics Digestive System Diseases - immunology Feature selection Gene Expression Profiling Humans Machine Learning Metabolic Diseases - genetics Metabolic Diseases - immunology Neoplasms - genetics Neoplasms - immunology Respiration Disorders - genetics Respiration Disorders - immunology Respiratory Tract Diseases - genetics Respiratory Tract Diseases - immunology |
title | Machine learning analysis of CD4+ T cell gene expression in diverse diseases: insights from cancer, metabolic, respiratory, and digestive disorders |
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