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...
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Veröffentlicht in: | Journal of investigative medicine 2012-04, Vol.60 (4), p.689-694 |
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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 |
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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 - 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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> |
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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 |
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