Increased CX3CL1 mRNA expression level is a positive prognostic factor in patients with lung adenocarcinoma
Chemokines are a family of small cytokines, which are signalling proteins secreted by cells. The principal role of chemokines is to serve as chemoattractants to guide the migration of their target cells. Chemokine C-X3-C motif ligand 1 (CX3CL1) is a protein-coding gene of fractalkine, which serves a...
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Veröffentlicht in: | Oncology letters 2019-06, Vol.17 (6), p.4877-4890 |
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creator | Liu, Jian Li, Yan Zhu, Xiaoqin Li, Qing Liang, Xiaohong Xie, Jun Hu, Song Peng, Wanda Li, Chong |
description | Chemokines are a family of small cytokines, which are signalling proteins secreted by cells. The principal role of chemokines is to serve as chemoattractants to guide the migration of their target cells. Chemokine C-X3-C motif ligand 1 (CX3CL1) is a protein-coding gene of fractalkine, which serves as a ligand for chemokine C-X3-C motif receptor 1 (CX3CR1) and integrins. However, the roles of CX3CL1 in different pathological types of lung cancer remain poorly understood. The present study aimed to investigate the potential clinical and biological function of CX3CL1 mRNA expression in patients with lung cancer. In the present study, lung cancer data obtained from the Gene Expression Omnibus database and The Cancer Genome Atlas were downloaded and analysed, and the results demonstrated that an increased CX3CL1 mRNA expression in tumour tissues from lung adenocarcinoma (LUAD) was associated with improved overall survival. However, no significant association was identified between CX3CL1 expression and the prognosis of lung squamous cell carcinoma (LUSC). Furthermore, the genes whose expression levels were correlated with CX3CL1 expression were subjected to enrichment analysis, and the results for the LUAD data demonstrated that the most significant biological processes included 'positive regulation of cell adhesion', 'leukocyte cell-cell adhesion', 'leukocyte migration' and 'T cell activation', whereas, the important highly ranked pathways included 'cell adhesion molecules (CAMs)', 'leukocyte transendothelial migration' and 'natural killer cell-mediated cytotoxicity'. However, in the patients with LUSC, the genes that were highly correlated with CX3CL1 were not enriched for any biological processes or signalling pathways. Based on the data of the present study, it was hypothesised that CX3CL1 may serve as a prognostic marker for LUAD. |
doi_str_mv | 10.3892/ol.2019.10211 |
format | Article |
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The principal role of chemokines is to serve as chemoattractants to guide the migration of their target cells. Chemokine C-X3-C motif ligand 1 (CX3CL1) is a protein-coding gene of fractalkine, which serves as a ligand for chemokine C-X3-C motif receptor 1 (CX3CR1) and integrins. However, the roles of CX3CL1 in different pathological types of lung cancer remain poorly understood. The present study aimed to investigate the potential clinical and biological function of CX3CL1 mRNA expression in patients with lung cancer. In the present study, lung cancer data obtained from the Gene Expression Omnibus database and The Cancer Genome Atlas were downloaded and analysed, and the results demonstrated that an increased CX3CL1 mRNA expression in tumour tissues from lung adenocarcinoma (LUAD) was associated with improved overall survival. However, no significant association was identified between CX3CL1 expression and the prognosis of lung squamous cell carcinoma (LUSC). Furthermore, the genes whose expression levels were correlated with CX3CL1 expression were subjected to enrichment analysis, and the results for the LUAD data demonstrated that the most significant biological processes included 'positive regulation of cell adhesion', 'leukocyte cell-cell adhesion', 'leukocyte migration' and 'T cell activation', whereas, the important highly ranked pathways included 'cell adhesion molecules (CAMs)', 'leukocyte transendothelial migration' and 'natural killer cell-mediated cytotoxicity'. However, in the patients with LUSC, the genes that were highly correlated with CX3CL1 were not enriched for any biological processes or signalling pathways. Based on the data of the present study, it was hypothesised that CX3CL1 may serve as a prognostic marker for LUAD.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2019.10211</identifier><identifier>PMID: 31186696</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Adenocarcinoma ; Anopheles ; Breast cancer ; Cancer cells ; Cancer patients ; Cancer research ; Cancer treatment ; Carcinoma ; Care and treatment ; Cell adhesion & migration ; Chemokines ; Confidence intervals ; Cytokines ; Datasets ; Gene expression ; Genes ; Genomes ; Genomics ; Integrins ; Killer cells ; Kinases ; Ligands ; Lung cancer ; Medical prognosis ; Messenger RNA ; Metastasis ; Multivariate analysis ; Oncology ; Ovarian cancer ; Patient outcomes ; Proteins ; Researchers ; RNA ; Software packages ; Squamous cell carcinoma ; Statistical analysis ; T cells ; Tumors</subject><ispartof>Oncology letters, 2019-06, Vol.17 (6), p.4877-4890</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Liu et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-c422c71e23a711c996174df462ea739690d7ce9207c0bc0e2008361a6a351edc3</citedby><cites>FETCH-LOGICAL-c513t-c422c71e23a711c996174df462ea739690d7ce9207c0bc0e2008361a6a351edc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507390/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507390/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31186696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Jian</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Zhu, Xiaoqin</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Liang, Xiaohong</creatorcontrib><creatorcontrib>Xie, Jun</creatorcontrib><creatorcontrib>Hu, Song</creatorcontrib><creatorcontrib>Peng, Wanda</creatorcontrib><creatorcontrib>Li, Chong</creatorcontrib><title>Increased CX3CL1 mRNA expression level is a positive prognostic factor in patients with lung adenocarcinoma</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Chemokines are a family of small cytokines, which are signalling proteins secreted by cells. The principal role of chemokines is to serve as chemoattractants to guide the migration of their target cells. Chemokine C-X3-C motif ligand 1 (CX3CL1) is a protein-coding gene of fractalkine, which serves as a ligand for chemokine C-X3-C motif receptor 1 (CX3CR1) and integrins. However, the roles of CX3CL1 in different pathological types of lung cancer remain poorly understood. The present study aimed to investigate the potential clinical and biological function of CX3CL1 mRNA expression in patients with lung cancer. In the present study, lung cancer data obtained from the Gene Expression Omnibus database and The Cancer Genome Atlas were downloaded and analysed, and the results demonstrated that an increased CX3CL1 mRNA expression in tumour tissues from lung adenocarcinoma (LUAD) was associated with improved overall survival. However, no significant association was identified between CX3CL1 expression and the prognosis of lung squamous cell carcinoma (LUSC). Furthermore, the genes whose expression levels were correlated with CX3CL1 expression were subjected to enrichment analysis, and the results for the LUAD data demonstrated that the most significant biological processes included 'positive regulation of cell adhesion', 'leukocyte cell-cell adhesion', 'leukocyte migration' and 'T cell activation', whereas, the important highly ranked pathways included 'cell adhesion molecules (CAMs)', 'leukocyte transendothelial migration' and 'natural killer cell-mediated cytotoxicity'. However, in the patients with LUSC, the genes that were highly correlated with CX3CL1 were not enriched for any biological processes or signalling pathways. Based on the data of the present study, it was hypothesised that CX3CL1 may serve as a prognostic marker for LUAD.</description><subject>Adenocarcinoma</subject><subject>Anopheles</subject><subject>Breast cancer</subject><subject>Cancer cells</subject><subject>Cancer patients</subject><subject>Cancer research</subject><subject>Cancer treatment</subject><subject>Carcinoma</subject><subject>Care and treatment</subject><subject>Cell adhesion & migration</subject><subject>Chemokines</subject><subject>Confidence intervals</subject><subject>Cytokines</subject><subject>Datasets</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Integrins</subject><subject>Killer cells</subject><subject>Kinases</subject><subject>Ligands</subject><subject>Lung cancer</subject><subject>Medical prognosis</subject><subject>Messenger RNA</subject><subject>Metastasis</subject><subject>Multivariate analysis</subject><subject>Oncology</subject><subject>Ovarian cancer</subject><subject>Patient outcomes</subject><subject>Proteins</subject><subject>Researchers</subject><subject>RNA</subject><subject>Software packages</subject><subject>Squamous cell carcinoma</subject><subject>Statistical analysis</subject><subject>T cells</subject><subject>Tumors</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptktFrFDEQxhdRbKl99FUCgviyZybZzW5ehOOoWjgURMG3kGZn71KzyZrsnva_b87WsycmDwmT33yTTL6ieA50wVvJ3gS3YBTkAigDeFScQiNZCbRljw_7pjopzlO6pnnUAtpWPC1OOEArhBSnxfdLbyLqhB1ZfeOrNZDh88clwV9jxJRs8MThDh2xiWgyhmQnu0MyxrDxIU3WkF6bKURiPRn1ZNFPify005a42W-I7tAHo6OxPgz6WfGk1y7h-f16Vnx9d_Fl9aFcf3p_uVquS1MDn0pTMWYaQMZ1A2CkFNBUXV8JhrrhUkjaNQYlo42hV4Yio7TlArTQvAbsDD8r3t7pjvPVkAP5UlE7NUY76Hijgrbq-MTbrdqEnRI1zQVoFnh9LxDDjxnTpAabDDqnPYY5KcYrSitBmzqjL_9Br8McfX6eYnlUXDIu_lIb7VBZ34dc1-xF1bJuBUAt6ypTi_9QeXY4WBM89jbHjxJePUjYonbTNgU3T_nf0jFY3oEmhpQi9odmAFV7J6ng1N5J6reTMv_iYQcP9B_f8Ft6wMFy</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Liu, Jian</creator><creator>Li, Yan</creator><creator>Zhu, Xiaoqin</creator><creator>Li, Qing</creator><creator>Liang, Xiaohong</creator><creator>Xie, Jun</creator><creator>Hu, Song</creator><creator>Peng, Wanda</creator><creator>Li, Chong</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190601</creationdate><title>Increased CX3CL1 mRNA expression level is a positive prognostic factor in patients with lung adenocarcinoma</title><author>Liu, Jian ; Li, Yan ; Zhu, Xiaoqin ; Li, Qing ; Liang, Xiaohong ; Xie, Jun ; Hu, Song ; Peng, Wanda ; Li, Chong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-c422c71e23a711c996174df462ea739690d7ce9207c0bc0e2008361a6a351edc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adenocarcinoma</topic><topic>Anopheles</topic><topic>Breast cancer</topic><topic>Cancer cells</topic><topic>Cancer patients</topic><topic>Cancer research</topic><topic>Cancer treatment</topic><topic>Carcinoma</topic><topic>Care and treatment</topic><topic>Cell adhesion & migration</topic><topic>Chemokines</topic><topic>Confidence intervals</topic><topic>Cytokines</topic><topic>Datasets</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Integrins</topic><topic>Killer cells</topic><topic>Kinases</topic><topic>Ligands</topic><topic>Lung cancer</topic><topic>Medical prognosis</topic><topic>Messenger RNA</topic><topic>Metastasis</topic><topic>Multivariate analysis</topic><topic>Oncology</topic><topic>Ovarian cancer</topic><topic>Patient outcomes</topic><topic>Proteins</topic><topic>Researchers</topic><topic>RNA</topic><topic>Software packages</topic><topic>Squamous cell carcinoma</topic><topic>Statistical analysis</topic><topic>T cells</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jian</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Zhu, Xiaoqin</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Liang, Xiaohong</creatorcontrib><creatorcontrib>Xie, Jun</creatorcontrib><creatorcontrib>Hu, Song</creatorcontrib><creatorcontrib>Peng, Wanda</creatorcontrib><creatorcontrib>Li, Chong</creatorcontrib><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>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>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jian</au><au>Li, Yan</au><au>Zhu, Xiaoqin</au><au>Li, Qing</au><au>Liang, Xiaohong</au><au>Xie, Jun</au><au>Hu, Song</au><au>Peng, Wanda</au><au>Li, Chong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased CX3CL1 mRNA expression level is a positive prognostic factor in patients with lung adenocarcinoma</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>17</volume><issue>6</issue><spage>4877</spage><epage>4890</epage><pages>4877-4890</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Chemokines are a family of small cytokines, which are signalling proteins secreted by cells. The principal role of chemokines is to serve as chemoattractants to guide the migration of their target cells. Chemokine C-X3-C motif ligand 1 (CX3CL1) is a protein-coding gene of fractalkine, which serves as a ligand for chemokine C-X3-C motif receptor 1 (CX3CR1) and integrins. However, the roles of CX3CL1 in different pathological types of lung cancer remain poorly understood. The present study aimed to investigate the potential clinical and biological function of CX3CL1 mRNA expression in patients with lung cancer. In the present study, lung cancer data obtained from the Gene Expression Omnibus database and The Cancer Genome Atlas were downloaded and analysed, and the results demonstrated that an increased CX3CL1 mRNA expression in tumour tissues from lung adenocarcinoma (LUAD) was associated with improved overall survival. However, no significant association was identified between CX3CL1 expression and the prognosis of lung squamous cell carcinoma (LUSC). Furthermore, the genes whose expression levels were correlated with CX3CL1 expression were subjected to enrichment analysis, and the results for the LUAD data demonstrated that the most significant biological processes included 'positive regulation of cell adhesion', 'leukocyte cell-cell adhesion', 'leukocyte migration' and 'T cell activation', whereas, the important highly ranked pathways included 'cell adhesion molecules (CAMs)', 'leukocyte transendothelial migration' and 'natural killer cell-mediated cytotoxicity'. However, in the patients with LUSC, the genes that were highly correlated with CX3CL1 were not enriched for any biological processes or signalling pathways. Based on the data of the present study, it was hypothesised that CX3CL1 may serve as a prognostic marker for LUAD.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>31186696</pmid><doi>10.3892/ol.2019.10211</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Anopheles Breast cancer Cancer cells Cancer patients Cancer research Cancer treatment Carcinoma Care and treatment Cell adhesion & migration Chemokines Confidence intervals Cytokines Datasets Gene expression Genes Genomes Genomics Integrins Killer cells Kinases Ligands Lung cancer Medical prognosis Messenger RNA Metastasis Multivariate analysis Oncology Ovarian cancer Patient outcomes Proteins Researchers RNA Software packages Squamous cell carcinoma Statistical analysis T cells Tumors |
title | Increased CX3CL1 mRNA expression level is a positive prognostic factor in patients with lung adenocarcinoma |
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