Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential

Human non–small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the developm...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of investigative medicine 2012-04, Vol.60 (4), p.689-694
Hauptverfasser: Sun, Wenjing, Guo, Changlong, Meng, Xiangning, Yu, Yang, Jin, Yan, Tong, Dandan, Geng, Jingshu, Huang, Qi, Qi, Jiping, Liu, An, Guan, Rongwei, Xu, Lidan, Sun, Donglin, Ji, Wei, Liu, Peng, Liu, Fangli, Sun, Haiming, Ji, Guohua, Fu, Songbin, Bai, Jing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 694
container_issue 4
container_start_page 689
container_title Journal of investigative medicine
container_volume 60
creator Sun, Wenjing
Guo, Changlong
Meng, Xiangning
Yu, Yang
Jin, Yan
Tong, Dandan
Geng, Jingshu
Huang, Qi
Qi, Jiping
Liu, An
Guan, Rongwei
Xu, Lidan
Sun, Donglin
Ji, Wei
Liu, Peng
Liu, Fangli
Sun, Haiming
Ji, Guohua
Fu, Songbin
Bai, Jing
description Human non–small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the development of lung cancer, the human giant cell lung carcinoma cell lines 95D with high metastatic potential and 95C with low metastatic potential were selected in this study. The 2 cell lines originated from the same parental cell and share a similar genetic background. In the current study, we identified 3 differentially expressed proteins in 95C and 95D cell lines, namely, PAI-RBP1, C1orf142, and COTL1, by using 2-dimensional electrophoresis proteomics analysis. We found that PAI-RBP1 and C1orf142 expression levels were higher in 95D than in 95C cells, whereas COTL1 expression level was lower in 95D when compared to 95C cells. We also confirmed these results by reverse transcription–polymerase chain reaction and immunoblotting analyses. The messenger RNA and protein levels of PAI-RBP1 and C1orf142 were much higher in 95D than in 95C cells, and COTL1 expression level was lower in 95D than in 95C cells. The PAI-RBP1 expression was assessed by immunohistochemistry in 70 NSCLC and 7 normal lung tissue samples from patients. PAI-RBP1 expression level was higher in tumor tissues (positive staining in 87.1% of cases [61/70]) than in normal tissues (positive staining in 14.3% of cases [1/7]). In conclusion, by studying protein expression in NSCLC cell lines with high and low metastasis as well as in human lung cancer tissues, we have identified 3 proteins, namely, PAI-RBP1, C1orf142, and COTL1, which were differentially expressed in NSCLC cell lines with different metastatic potential. In addition, we also found that PAI-RBP1 might contribute to NSCLC development.
doi_str_mv 10.2310/JIM.0b013e31824963b6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_934265648</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.2310_JIM.0b013e31824963b6</sage_id><sourcerecordid>934265648</sourcerecordid><originalsourceid>FETCH-LOGICAL-b346t-787fba5abb0355b3b423b33fdcf7b27a3b3e7f39d87ff49b52ab00b97219fef43</originalsourceid><addsrcrecordid>eNqNkc1O3DAUhS1Exf8bVJUlFmwI-C9xvKQByqChjNpBXUZ2xqYeTeypnUiw4wVY9Q15khplQIhFxca-1_ruuUc-AHzG6IhQjI4vR1dHSCFMNcUlYaKgqlgDW5ijMitJwddTjUqc5XkpNsF2jHOESJELsgE2CaGcpnoLPJ5aY3TQrrNyAc_ulkHHaL2D3sDJySj78XWCD2GFfTCYkUMo3QxW19MxhtbB7949Pfz92crFAlY6HePe3cJKukaH1YN1OsJftvsNXxfBad_6AK90J2MnO9vAie8GA7vgk5GLqPdW9w64OT-bVhfZ-PrbqDoZZ4qyost4yY2SuVQK0TxXVDFCFaVm1hiuCJep0dxQMUucYULlRCqElOAEC6MNozvgYNBdBv-n17GrWxubZFg67ftYC8rSVxWsTOT-O3Lu--CSuRrzshCEI4wTxQaqCT7GoE29DLaV4b7GqH5Oq05p1e_TSmNfVuK9avXsdeglngTgAYjyVr_Z_H_R42FGtfOP2fgH3CGs2A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1786927011</pqid></control><display><type>article</type><title>Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential</title><source>MEDLINE</source><source>SAGE Complete</source><creator>Sun, Wenjing ; Guo, Changlong ; Meng, Xiangning ; Yu, Yang ; Jin, Yan ; Tong, Dandan ; Geng, Jingshu ; Huang, Qi ; Qi, Jiping ; Liu, An ; Guan, Rongwei ; Xu, Lidan ; Sun, Donglin ; Ji, Wei ; Liu, Peng ; Liu, Fangli ; Sun, Haiming ; Ji, Guohua ; Fu, Songbin ; Bai, Jing</creator><creatorcontrib>Sun, Wenjing ; Guo, Changlong ; Meng, Xiangning ; Yu, Yang ; Jin, Yan ; Tong, Dandan ; Geng, Jingshu ; Huang, Qi ; Qi, Jiping ; Liu, An ; Guan, Rongwei ; Xu, Lidan ; Sun, Donglin ; Ji, Wei ; Liu, Peng ; Liu, Fangli ; Sun, Haiming ; Ji, Guohua ; Fu, Songbin ; Bai, Jing</creatorcontrib><description>Human non–small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the development of lung cancer, the human giant cell lung carcinoma cell lines 95D with high metastatic potential and 95C with low metastatic potential were selected in this study. The 2 cell lines originated from the same parental cell and share a similar genetic background. In the current study, we identified 3 differentially expressed proteins in 95C and 95D cell lines, namely, PAI-RBP1, C1orf142, and COTL1, by using 2-dimensional electrophoresis proteomics analysis. We found that PAI-RBP1 and C1orf142 expression levels were higher in 95D than in 95C cells, whereas COTL1 expression level was lower in 95D when compared to 95C cells. We also confirmed these results by reverse transcription–polymerase chain reaction and immunoblotting analyses. The messenger RNA and protein levels of PAI-RBP1 and C1orf142 were much higher in 95D than in 95C cells, and COTL1 expression level was lower in 95D than in 95C cells. The PAI-RBP1 expression was assessed by immunohistochemistry in 70 NSCLC and 7 normal lung tissue samples from patients. PAI-RBP1 expression level was higher in tumor tissues (positive staining in 87.1% of cases [61/70]) than in normal tissues (positive staining in 14.3% of cases [1/7]). In conclusion, by studying protein expression in NSCLC cell lines with high and low metastasis as well as in human lung cancer tissues, we have identified 3 proteins, namely, PAI-RBP1, C1orf142, and COTL1, which were differentially expressed in NSCLC cell lines with different metastatic potential. In addition, we also found that PAI-RBP1 might contribute to NSCLC development.</description><identifier>ISSN: 1081-5589</identifier><identifier>EISSN: 1708-8267</identifier><identifier>DOI: 10.2310/JIM.0b013e31824963b6</identifier><identifier>PMID: 22373659</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Line, Tumor ; Gene Expression Regulation, Neoplastic ; Humans ; Lung cancer ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Microfilament Proteins - biosynthesis ; Microfilament Proteins - genetics ; Qb-SNARE Proteins - biosynthesis ; Qb-SNARE Proteins - genetics ; Qc-SNARE Proteins - biosynthesis ; Qc-SNARE Proteins - genetics ; RNA-Binding Proteins - biosynthesis ; RNA-Binding Proteins - genetics</subject><ispartof>Journal of investigative medicine, 2012-04, Vol.60 (4), p.689-694</ispartof><rights>2015 American Federation for Medical Research, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2012 American Federation for Medical Research</rights><rights>Copyright: 2015 (c) 2015 American Federation for Medical Research, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b346t-787fba5abb0355b3b423b33fdcf7b27a3b3e7f39d87ff49b52ab00b97219fef43</citedby><cites>FETCH-LOGICAL-b346t-787fba5abb0355b3b423b33fdcf7b27a3b3e7f39d87ff49b52ab00b97219fef43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.2310/JIM.0b013e31824963b6$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.2310/JIM.0b013e31824963b6$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22373659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Wenjing</creatorcontrib><creatorcontrib>Guo, Changlong</creatorcontrib><creatorcontrib>Meng, Xiangning</creatorcontrib><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Jin, Yan</creatorcontrib><creatorcontrib>Tong, Dandan</creatorcontrib><creatorcontrib>Geng, Jingshu</creatorcontrib><creatorcontrib>Huang, Qi</creatorcontrib><creatorcontrib>Qi, Jiping</creatorcontrib><creatorcontrib>Liu, An</creatorcontrib><creatorcontrib>Guan, Rongwei</creatorcontrib><creatorcontrib>Xu, Lidan</creatorcontrib><creatorcontrib>Sun, Donglin</creatorcontrib><creatorcontrib>Ji, Wei</creatorcontrib><creatorcontrib>Liu, Peng</creatorcontrib><creatorcontrib>Liu, Fangli</creatorcontrib><creatorcontrib>Sun, Haiming</creatorcontrib><creatorcontrib>Ji, Guohua</creatorcontrib><creatorcontrib>Fu, Songbin</creatorcontrib><creatorcontrib>Bai, Jing</creatorcontrib><title>Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential</title><title>Journal of investigative medicine</title><addtitle>J Investig Med</addtitle><description>Human non–small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the development of lung cancer, the human giant cell lung carcinoma cell lines 95D with high metastatic potential and 95C with low metastatic potential were selected in this study. The 2 cell lines originated from the same parental cell and share a similar genetic background. In the current study, we identified 3 differentially expressed proteins in 95C and 95D cell lines, namely, PAI-RBP1, C1orf142, and COTL1, by using 2-dimensional electrophoresis proteomics analysis. We found that PAI-RBP1 and C1orf142 expression levels were higher in 95D than in 95C cells, whereas COTL1 expression level was lower in 95D when compared to 95C cells. We also confirmed these results by reverse transcription–polymerase chain reaction and immunoblotting analyses. The messenger RNA and protein levels of PAI-RBP1 and C1orf142 were much higher in 95D than in 95C cells, and COTL1 expression level was lower in 95D than in 95C cells. The PAI-RBP1 expression was assessed by immunohistochemistry in 70 NSCLC and 7 normal lung tissue samples from patients. PAI-RBP1 expression level was higher in tumor tissues (positive staining in 87.1% of cases [61/70]) than in normal tissues (positive staining in 14.3% of cases [1/7]). In conclusion, by studying protein expression in NSCLC cell lines with high and low metastasis as well as in human lung cancer tissues, we have identified 3 proteins, namely, PAI-RBP1, C1orf142, and COTL1, which were differentially expressed in NSCLC cell lines with different metastatic potential. In addition, we also found that PAI-RBP1 might contribute to NSCLC development.</description><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Line, Tumor</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Microfilament Proteins - biosynthesis</subject><subject>Microfilament Proteins - genetics</subject><subject>Qb-SNARE Proteins - biosynthesis</subject><subject>Qb-SNARE Proteins - genetics</subject><subject>Qc-SNARE Proteins - biosynthesis</subject><subject>Qc-SNARE Proteins - genetics</subject><subject>RNA-Binding Proteins - biosynthesis</subject><subject>RNA-Binding Proteins - genetics</subject><issn>1081-5589</issn><issn>1708-8267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkc1O3DAUhS1Exf8bVJUlFmwI-C9xvKQByqChjNpBXUZ2xqYeTeypnUiw4wVY9Q15khplQIhFxca-1_ruuUc-AHzG6IhQjI4vR1dHSCFMNcUlYaKgqlgDW5ijMitJwddTjUqc5XkpNsF2jHOESJELsgE2CaGcpnoLPJ5aY3TQrrNyAc_ulkHHaL2D3sDJySj78XWCD2GFfTCYkUMo3QxW19MxhtbB7949Pfz92crFAlY6HePe3cJKukaH1YN1OsJftvsNXxfBad_6AK90J2MnO9vAie8GA7vgk5GLqPdW9w64OT-bVhfZ-PrbqDoZZ4qyost4yY2SuVQK0TxXVDFCFaVm1hiuCJep0dxQMUucYULlRCqElOAEC6MNozvgYNBdBv-n17GrWxubZFg67ftYC8rSVxWsTOT-O3Lu--CSuRrzshCEI4wTxQaqCT7GoE29DLaV4b7GqH5Oq05p1e_TSmNfVuK9avXsdeglngTgAYjyVr_Z_H_R42FGtfOP2fgH3CGs2A</recordid><startdate>201204</startdate><enddate>201204</enddate><creator>Sun, Wenjing</creator><creator>Guo, Changlong</creator><creator>Meng, Xiangning</creator><creator>Yu, Yang</creator><creator>Jin, Yan</creator><creator>Tong, Dandan</creator><creator>Geng, Jingshu</creator><creator>Huang, Qi</creator><creator>Qi, Jiping</creator><creator>Liu, An</creator><creator>Guan, Rongwei</creator><creator>Xu, Lidan</creator><creator>Sun, Donglin</creator><creator>Ji, Wei</creator><creator>Liu, Peng</creator><creator>Liu, Fangli</creator><creator>Sun, Haiming</creator><creator>Ji, Guohua</creator><creator>Fu, Songbin</creator><creator>Bai, Jing</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AM</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGRYB</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K7.</scope><scope>K9.</scope><scope>M0O</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201204</creationdate><title>Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential</title><author>Sun, Wenjing ; Guo, Changlong ; Meng, Xiangning ; Yu, Yang ; Jin, Yan ; Tong, Dandan ; Geng, Jingshu ; Huang, Qi ; Qi, Jiping ; Liu, An ; Guan, Rongwei ; Xu, Lidan ; Sun, Donglin ; Ji, Wei ; Liu, Peng ; Liu, Fangli ; Sun, Haiming ; Ji, Guohua ; Fu, Songbin ; Bai, Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b346t-787fba5abb0355b3b423b33fdcf7b27a3b3e7f39d87ff49b52ab00b97219fef43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Line, Tumor</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Microfilament Proteins - biosynthesis</topic><topic>Microfilament Proteins - genetics</topic><topic>Qb-SNARE Proteins - biosynthesis</topic><topic>Qb-SNARE Proteins - genetics</topic><topic>Qc-SNARE Proteins - biosynthesis</topic><topic>Qc-SNARE Proteins - genetics</topic><topic>RNA-Binding Proteins - biosynthesis</topic><topic>RNA-Binding Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Wenjing</creatorcontrib><creatorcontrib>Guo, Changlong</creatorcontrib><creatorcontrib>Meng, Xiangning</creatorcontrib><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Jin, Yan</creatorcontrib><creatorcontrib>Tong, Dandan</creatorcontrib><creatorcontrib>Geng, Jingshu</creatorcontrib><creatorcontrib>Huang, Qi</creatorcontrib><creatorcontrib>Qi, Jiping</creatorcontrib><creatorcontrib>Liu, An</creatorcontrib><creatorcontrib>Guan, Rongwei</creatorcontrib><creatorcontrib>Xu, Lidan</creatorcontrib><creatorcontrib>Sun, Donglin</creatorcontrib><creatorcontrib>Ji, Wei</creatorcontrib><creatorcontrib>Liu, Peng</creatorcontrib><creatorcontrib>Liu, Fangli</creatorcontrib><creatorcontrib>Sun, Haiming</creatorcontrib><creatorcontrib>Ji, Guohua</creatorcontrib><creatorcontrib>Fu, Songbin</creatorcontrib><creatorcontrib>Bai, Jing</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 Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Criminal Justice Database (Alumni Edition)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Criminology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>ProQuest Criminal Justice (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Criminal Justice</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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 Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of investigative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Wenjing</au><au>Guo, Changlong</au><au>Meng, Xiangning</au><au>Yu, Yang</au><au>Jin, Yan</au><au>Tong, Dandan</au><au>Geng, Jingshu</au><au>Huang, Qi</au><au>Qi, Jiping</au><au>Liu, An</au><au>Guan, Rongwei</au><au>Xu, Lidan</au><au>Sun, Donglin</au><au>Ji, Wei</au><au>Liu, Peng</au><au>Liu, Fangli</au><au>Sun, Haiming</au><au>Ji, Guohua</au><au>Fu, Songbin</au><au>Bai, Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential</atitle><jtitle>Journal of investigative medicine</jtitle><addtitle>J Investig Med</addtitle><date>2012-04</date><risdate>2012</risdate><volume>60</volume><issue>4</issue><spage>689</spage><epage>694</epage><pages>689-694</pages><issn>1081-5589</issn><eissn>1708-8267</eissn><abstract>Human non–small cell lung cancer (NSCLC) is one of the most common malignancies in the modern world. Its recurrence is mainly due to its ability to invade and metastasize. However, the precise mechanism for tumor development and metastasis is still not fully understood. To shed light on the development of lung cancer, the human giant cell lung carcinoma cell lines 95D with high metastatic potential and 95C with low metastatic potential were selected in this study. The 2 cell lines originated from the same parental cell and share a similar genetic background. In the current study, we identified 3 differentially expressed proteins in 95C and 95D cell lines, namely, PAI-RBP1, C1orf142, and COTL1, by using 2-dimensional electrophoresis proteomics analysis. We found that PAI-RBP1 and C1orf142 expression levels were higher in 95D than in 95C cells, whereas COTL1 expression level was lower in 95D when compared to 95C cells. We also confirmed these results by reverse transcription–polymerase chain reaction and immunoblotting analyses. The messenger RNA and protein levels of PAI-RBP1 and C1orf142 were much higher in 95D than in 95C cells, and COTL1 expression level was lower in 95D than in 95C cells. The PAI-RBP1 expression was assessed by immunohistochemistry in 70 NSCLC and 7 normal lung tissue samples from patients. PAI-RBP1 expression level was higher in tumor tissues (positive staining in 87.1% of cases [61/70]) than in normal tissues (positive staining in 14.3% of cases [1/7]). In conclusion, by studying protein expression in NSCLC cell lines with high and low metastasis as well as in human lung cancer tissues, we have identified 3 proteins, namely, PAI-RBP1, C1orf142, and COTL1, which were differentially expressed in NSCLC cell lines with different metastatic potential. In addition, we also found that PAI-RBP1 might contribute to NSCLC development.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>22373659</pmid><doi>10.2310/JIM.0b013e31824963b6</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1081-5589
ispartof Journal of investigative medicine, 2012-04, Vol.60 (4), p.689-694
issn 1081-5589
1708-8267
language eng
recordid cdi_proquest_miscellaneous_934265648
source MEDLINE; SAGE Complete
subjects Carcinoma, Non-Small-Cell Lung - metabolism
Carcinoma, Non-Small-Cell Lung - pathology
Cell Line, Tumor
Gene Expression Regulation, Neoplastic
Humans
Lung cancer
Lung Neoplasms - metabolism
Lung Neoplasms - pathology
Microfilament Proteins - biosynthesis
Microfilament Proteins - genetics
Qb-SNARE Proteins - biosynthesis
Qb-SNARE Proteins - genetics
Qc-SNARE Proteins - biosynthesis
Qc-SNARE Proteins - genetics
RNA-Binding Proteins - biosynthesis
RNA-Binding Proteins - genetics
title Differential Expression of PAI-RBP1, C1orf142, and COTL1 in Non–Small Cell Lung Cancer Cell Lines With Different Tumor Metastatic Potential
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T06%3A14%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20Expression%20of%20PAI-RBP1,%20C1orf142,%20and%20COTL1%20in%20Non%E2%80%93Small%20Cell%20Lung%20Cancer%20Cell%20Lines%20With%20Different%20Tumor%20Metastatic%20Potential&rft.jtitle=Journal%20of%20investigative%20medicine&rft.au=Sun,%20Wenjing&rft.date=2012-04&rft.volume=60&rft.issue=4&rft.spage=689&rft.epage=694&rft.pages=689-694&rft.issn=1081-5589&rft.eissn=1708-8267&rft_id=info:doi/10.2310/JIM.0b013e31824963b6&rft_dat=%3Cproquest_cross%3E934265648%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1786927011&rft_id=info:pmid/22373659&rft_sage_id=10.2310_JIM.0b013e31824963b6&rfr_iscdi=true