Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning
Purpose The objective of this study was to investigate the key glycolysis-related genes linked to immune cell infiltration in endometriosis and to develop a new endometriosis (EMS) predictive model. Methods A training set and a test set were created from the Gene Expression Omnibus (GEO) public data...
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Veröffentlicht in: | Journal of assisted reproduction and genetics 2023-05, Vol.40 (5), p.1147-1161 |
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creator | Chen, Qizhen Jiao, Yufan Yin, Zhe Fu, Xiayan Guo, Shana Zhou, Yuhua Wang, Yanqiu |
description | Purpose
The objective of this study was to investigate the key glycolysis-related genes linked to immune cell infiltration in endometriosis and to develop a new endometriosis (EMS) predictive model.
Methods
A training set and a test set were created from the Gene Expression Omnibus (GEO) public database. We identified five glycolysis-related genes using least absolute shrinkage and selection operator (LASSO) regression and the random forest method. Then, we developed and tested a prediction model for EMS diagnosis. The CIBERSORT method was used to compare the infiltration of 22 different immune cells. We examined the relationship between key glycolysis-related genes and immune factors in the eutopic endometrium of women with endometriosis. In addition, Gene Ontology (GO)-based semantic similarity and logistic regression model analyses were used to investigate core genes. Reverse real-time quantitative PCR (RT-qPCR) of 5 target genes was analysed.
Results
The five glycolysis-related hub genes (CHPF, CITED2, GPC3, PDK3, ADH6) were used to establish a predictive model for EMS. In the training and test sets, the area under the curve (AUC) of the receiver operating characteristic curve (ROC) prediction model was 0.777, 0.824, and 0.774. Additionally, there was a remarkable difference in the immune environment between the EMS and control groups. Eventually, the five target genes were verified by RT-qPCR.
Conclusion
The glycolysis-immune-based predictive model was established to forecast EMS patients’ diagnosis, and a detailed comprehension of the interactions between endometriosis, glycolysis, and the immune system may be vital for the recognition of potential novel therapeutic approaches and targets for EMS patients. |
doi_str_mv | 10.1007/s10815-023-02769-0 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10239430</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2821995964</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-8081619c02d7f99594944ba53fdea91fa04ee00853201e48b88729f7a13311483</originalsourceid><addsrcrecordid>eNp9kc1u1TAQhS0EouXCC7BAltiwCYxjJ7ZXCFWlIFViA2vLSSa5rhy7tZNK9-3r9LblZ8HCsqX5PHPOHELeMvjIAOSnzECxpoKalyNbXcEzcsoaySvJOTwvb2hUBaJVJ-RVzlcAoFXNX5IT3moOvNGn5OY8L7bzLu9nDAuNI7U0xFv0dPKHPvpDdrly87wGrBJ6u-BAB2enEEuBThiQZjcFu6wJ6RgTxTDEGZfk7oHuQGfb713BPNoUXJhekxej9RnfPNw78uvr-c-zb9Xlj4vvZ18uq17IZqlU8dYy3UM9yFHrRgstRGcbPg5oNRstCEQA1fAaGArVKSVrPUrLOGdMKL4jn499r9duxqEv9pL15jq52aaDidaZvyvB7c0Ubw0rC9Wi7GdHPjx0SPFmxbyY2eUevbcB45pNreqaSy31Nuz9P-hVXFMo_jaKbfpbUaj6SPUp5pxwfFLDwGyRmmOkpigw95GaTcW7P308fXnMsAD8CORSChOm37P_0_YOlUCt7Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2821995964</pqid></control><display><type>article</type><title>Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><creator>Chen, Qizhen ; Jiao, Yufan ; Yin, Zhe ; Fu, Xiayan ; Guo, Shana ; Zhou, Yuhua ; Wang, Yanqiu</creator><creatorcontrib>Chen, Qizhen ; Jiao, Yufan ; Yin, Zhe ; Fu, Xiayan ; Guo, Shana ; Zhou, Yuhua ; Wang, Yanqiu</creatorcontrib><description>Purpose
The objective of this study was to investigate the key glycolysis-related genes linked to immune cell infiltration in endometriosis and to develop a new endometriosis (EMS) predictive model.
Methods
A training set and a test set were created from the Gene Expression Omnibus (GEO) public database. We identified five glycolysis-related genes using least absolute shrinkage and selection operator (LASSO) regression and the random forest method. Then, we developed and tested a prediction model for EMS diagnosis. The CIBERSORT method was used to compare the infiltration of 22 different immune cells. We examined the relationship between key glycolysis-related genes and immune factors in the eutopic endometrium of women with endometriosis. In addition, Gene Ontology (GO)-based semantic similarity and logistic regression model analyses were used to investigate core genes. Reverse real-time quantitative PCR (RT-qPCR) of 5 target genes was analysed.
Results
The five glycolysis-related hub genes (CHPF, CITED2, GPC3, PDK3, ADH6) were used to establish a predictive model for EMS. In the training and test sets, the area under the curve (AUC) of the receiver operating characteristic curve (ROC) prediction model was 0.777, 0.824, and 0.774. Additionally, there was a remarkable difference in the immune environment between the EMS and control groups. Eventually, the five target genes were verified by RT-qPCR.
Conclusion
The glycolysis-immune-based predictive model was established to forecast EMS patients’ diagnosis, and a detailed comprehension of the interactions between endometriosis, glycolysis, and the immune system may be vital for the recognition of potential novel therapeutic approaches and targets for EMS patients.</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-023-02769-0</identifier><identifier>PMID: 36930359</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Diagnosis ; Endometriosis ; Endometrium ; Gene expression ; Genes ; Glycolysis ; Gynecology ; Human Genetics ; Immune system ; Infiltration ; Medicine ; Medicine & Public Health ; Prediction models ; Reproductive Medicine ; Reproductive Physiology and Disease</subject><ispartof>Journal of assisted reproduction and genetics, 2023-05, Vol.40 (5), p.1147-1161</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-8081619c02d7f99594944ba53fdea91fa04ee00853201e48b88729f7a13311483</citedby><cites>FETCH-LOGICAL-c475t-8081619c02d7f99594944ba53fdea91fa04ee00853201e48b88729f7a13311483</cites><orcidid>0000-0001-9340-970X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239430/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239430/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36930359$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Qizhen</creatorcontrib><creatorcontrib>Jiao, Yufan</creatorcontrib><creatorcontrib>Yin, Zhe</creatorcontrib><creatorcontrib>Fu, Xiayan</creatorcontrib><creatorcontrib>Guo, Shana</creatorcontrib><creatorcontrib>Zhou, Yuhua</creatorcontrib><creatorcontrib>Wang, Yanqiu</creatorcontrib><title>Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><addtitle>J Assist Reprod Genet</addtitle><description>Purpose
The objective of this study was to investigate the key glycolysis-related genes linked to immune cell infiltration in endometriosis and to develop a new endometriosis (EMS) predictive model.
Methods
A training set and a test set were created from the Gene Expression Omnibus (GEO) public database. We identified five glycolysis-related genes using least absolute shrinkage and selection operator (LASSO) regression and the random forest method. Then, we developed and tested a prediction model for EMS diagnosis. The CIBERSORT method was used to compare the infiltration of 22 different immune cells. We examined the relationship between key glycolysis-related genes and immune factors in the eutopic endometrium of women with endometriosis. In addition, Gene Ontology (GO)-based semantic similarity and logistic regression model analyses were used to investigate core genes. Reverse real-time quantitative PCR (RT-qPCR) of 5 target genes was analysed.
Results
The five glycolysis-related hub genes (CHPF, CITED2, GPC3, PDK3, ADH6) were used to establish a predictive model for EMS. In the training and test sets, the area under the curve (AUC) of the receiver operating characteristic curve (ROC) prediction model was 0.777, 0.824, and 0.774. Additionally, there was a remarkable difference in the immune environment between the EMS and control groups. Eventually, the five target genes were verified by RT-qPCR.
Conclusion
The glycolysis-immune-based predictive model was established to forecast EMS patients’ diagnosis, and a detailed comprehension of the interactions between endometriosis, glycolysis, and the immune system may be vital for the recognition of potential novel therapeutic approaches and targets for EMS patients.</description><subject>Diagnosis</subject><subject>Endometriosis</subject><subject>Endometrium</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glycolysis</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Immune system</subject><subject>Infiltration</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Prediction models</subject><subject>Reproductive Medicine</subject><subject>Reproductive Physiology and Disease</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1u1TAQhS0EouXCC7BAltiwCYxjJ7ZXCFWlIFViA2vLSSa5rhy7tZNK9-3r9LblZ8HCsqX5PHPOHELeMvjIAOSnzECxpoKalyNbXcEzcsoaySvJOTwvb2hUBaJVJ-RVzlcAoFXNX5IT3moOvNGn5OY8L7bzLu9nDAuNI7U0xFv0dPKHPvpDdrly87wGrBJ6u-BAB2enEEuBThiQZjcFu6wJ6RgTxTDEGZfk7oHuQGfb713BPNoUXJhekxej9RnfPNw78uvr-c-zb9Xlj4vvZ18uq17IZqlU8dYy3UM9yFHrRgstRGcbPg5oNRstCEQA1fAaGArVKSVrPUrLOGdMKL4jn499r9duxqEv9pL15jq52aaDidaZvyvB7c0Ubw0rC9Wi7GdHPjx0SPFmxbyY2eUevbcB45pNreqaSy31Nuz9P-hVXFMo_jaKbfpbUaj6SPUp5pxwfFLDwGyRmmOkpigw95GaTcW7P308fXnMsAD8CORSChOm37P_0_YOlUCt7Q</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Chen, Qizhen</creator><creator>Jiao, Yufan</creator><creator>Yin, Zhe</creator><creator>Fu, Xiayan</creator><creator>Guo, Shana</creator><creator>Zhou, Yuhua</creator><creator>Wang, Yanqiu</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9340-970X</orcidid></search><sort><creationdate>20230501</creationdate><title>Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning</title><author>Chen, Qizhen ; Jiao, Yufan ; Yin, Zhe ; Fu, Xiayan ; Guo, Shana ; Zhou, Yuhua ; Wang, Yanqiu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-8081619c02d7f99594944ba53fdea91fa04ee00853201e48b88729f7a13311483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Diagnosis</topic><topic>Endometriosis</topic><topic>Endometrium</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Glycolysis</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Immune system</topic><topic>Infiltration</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Prediction models</topic><topic>Reproductive Medicine</topic><topic>Reproductive Physiology and Disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Qizhen</creatorcontrib><creatorcontrib>Jiao, Yufan</creatorcontrib><creatorcontrib>Yin, Zhe</creatorcontrib><creatorcontrib>Fu, Xiayan</creatorcontrib><creatorcontrib>Guo, Shana</creatorcontrib><creatorcontrib>Zhou, Yuhua</creatorcontrib><creatorcontrib>Wang, Yanqiu</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Qizhen</au><au>Jiao, Yufan</au><au>Yin, Zhe</au><au>Fu, Xiayan</au><au>Guo, Shana</au><au>Zhou, Yuhua</au><au>Wang, Yanqiu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><addtitle>J Assist Reprod Genet</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>40</volume><issue>5</issue><spage>1147</spage><epage>1161</epage><pages>1147-1161</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose
The objective of this study was to investigate the key glycolysis-related genes linked to immune cell infiltration in endometriosis and to develop a new endometriosis (EMS) predictive model.
Methods
A training set and a test set were created from the Gene Expression Omnibus (GEO) public database. We identified five glycolysis-related genes using least absolute shrinkage and selection operator (LASSO) regression and the random forest method. Then, we developed and tested a prediction model for EMS diagnosis. The CIBERSORT method was used to compare the infiltration of 22 different immune cells. We examined the relationship between key glycolysis-related genes and immune factors in the eutopic endometrium of women with endometriosis. In addition, Gene Ontology (GO)-based semantic similarity and logistic regression model analyses were used to investigate core genes. Reverse real-time quantitative PCR (RT-qPCR) of 5 target genes was analysed.
Results
The five glycolysis-related hub genes (CHPF, CITED2, GPC3, PDK3, ADH6) were used to establish a predictive model for EMS. In the training and test sets, the area under the curve (AUC) of the receiver operating characteristic curve (ROC) prediction model was 0.777, 0.824, and 0.774. Additionally, there was a remarkable difference in the immune environment between the EMS and control groups. Eventually, the five target genes were verified by RT-qPCR.
Conclusion
The glycolysis-immune-based predictive model was established to forecast EMS patients’ diagnosis, and a detailed comprehension of the interactions between endometriosis, glycolysis, and the immune system may be vital for the recognition of potential novel therapeutic approaches and targets for EMS patients.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36930359</pmid><doi>10.1007/s10815-023-02769-0</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-9340-970X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Diagnosis Endometriosis Endometrium Gene expression Genes Glycolysis Gynecology Human Genetics Immune system Infiltration Medicine Medicine & Public Health Prediction models Reproductive Medicine Reproductive Physiology and Disease |
title | Establishment of a novel glycolysis-immune-related diagnosis gene signature for endometriosis by machine learning |
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