Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile
Claudin proteins are components of epithelial tight junctions; a subtype of breast cancer has been defined by the reduced expression of mRNA for claudins and other genes. Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatograph...
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Veröffentlicht in: | Journal of proteome research 2017-04, Vol.16 (4), p.1391-1400 |
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description | Claudin proteins are components of epithelial tight junctions; a subtype of breast cancer has been defined by the reduced expression of mRNA for claudins and other genes. Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatography/tandem mass spectrometry. Unsupervised clustering techniques reveal a group of claudin-low cell lines that is distinct from nonmalignant, basal, and luminal lines. The claudin-low cell lines express F11R, EPCAM, and other proteins at very low levels, whereas CD44 is expressed at a high level. Comparison of mRNA expression to glycoprotein expression shows modest correlation; the best agreement occurs when the mRNA expression level is lowest and little or no protein is detected. These findings from cell lines are compared to those for tumor samples by the Clinical Proteomic Tumor Analysis Consortium (CPTAC). The CPTAC samples contain a group low in CLDN3. The samples low in CLDN3 proteins share many differentially expressed glycoproteins with the claudin-low cell lines. In contrast to the situation for cell lines or patient samples classified as claudin-low by RNA expression, however, most of the tumor samples low in CLDN3 protein express the estrogen receptor or HER2. These tumor samples express CD44 protein at low rather than high levels. There is no correlation between CLDN3 gene expression and protein expression in these CPTAC samples; hence, the claudin-low subtype defined by gene expression is not the same group of tumors as that defined by low expression of CLDN3 protein. |
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Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatography/tandem mass spectrometry. Unsupervised clustering techniques reveal a group of claudin-low cell lines that is distinct from nonmalignant, basal, and luminal lines. The claudin-low cell lines express F11R, EPCAM, and other proteins at very low levels, whereas CD44 is expressed at a high level. Comparison of mRNA expression to glycoprotein expression shows modest correlation; the best agreement occurs when the mRNA expression level is lowest and little or no protein is detected. These findings from cell lines are compared to those for tumor samples by the Clinical Proteomic Tumor Analysis Consortium (CPTAC). The CPTAC samples contain a group low in CLDN3. The samples low in CLDN3 proteins share many differentially expressed glycoproteins with the claudin-low cell lines. In contrast to the situation for cell lines or patient samples classified as claudin-low by RNA expression, however, most of the tumor samples low in CLDN3 protein express the estrogen receptor or HER2. These tumor samples express CD44 protein at low rather than high levels. There is no correlation between CLDN3 gene expression and protein expression in these CPTAC samples; hence, the claudin-low subtype defined by gene expression is not the same group of tumors as that defined by low expression of CLDN3 protein.</description><identifier>ISSN: 1535-3893</identifier><identifier>ISSN: 1535-3907</identifier><identifier>EISSN: 1535-3907</identifier><identifier>DOI: 10.1021/acs.jproteome.6b00470</identifier><identifier>PMID: 28287265</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Biomarkers, Tumor - biosynthesis ; Biomarkers, Tumor - genetics ; breast neoplasms ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; breasts ; Cell Line, Tumor ; cell lines ; Claudin-3 - biosynthesis ; Claudin-3 - genetics ; epithelium ; estrogen receptors ; Female ; gene expression ; Gene Expression Regulation, Neoplastic ; genes ; glycoproteins ; Glycoproteins - biosynthesis ; Glycoproteins - genetics ; Humans ; Hyaluronan Receptors - biosynthesis ; Hyaluronan Receptors - genetics ; liquid chromatography ; Mass Spectrometry - methods ; messenger RNA ; patients ; Prognosis ; protein synthesis ; proteome ; Proteomics ; Receptor, ErbB-2 - biosynthesis ; Receptor, ErbB-2 - genetics ; tandem mass spectrometry ; tight junctions</subject><ispartof>Journal of proteome research, 2017-04, Vol.16 (4), p.1391-1400</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a486t-4aab79eda3d68c0630aed0afc5bdb11a60ce26cf732bd5524e3a6cf1a9063e7f3</citedby><cites>FETCH-LOGICAL-a486t-4aab79eda3d68c0630aed0afc5bdb11a60ce26cf732bd5524e3a6cf1a9063e7f3</cites><orcidid>0000-0002-2398-4765</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jproteome.6b00470$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jproteome.6b00470$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2751,27055,27903,27904,56717,56767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28287265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yen, Ten-Yang</creatorcontrib><creatorcontrib>Bowen, Spencer</creatorcontrib><creatorcontrib>Yen, Roger</creatorcontrib><creatorcontrib>Piryatinska, Alexandra</creatorcontrib><creatorcontrib>Macher, Bruce A</creatorcontrib><creatorcontrib>Timpe, Leslie C</creatorcontrib><title>Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile</title><title>Journal of proteome research</title><addtitle>J. Proteome Res</addtitle><description>Claudin proteins are components of epithelial tight junctions; a subtype of breast cancer has been defined by the reduced expression of mRNA for claudins and other genes. Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatography/tandem mass spectrometry. Unsupervised clustering techniques reveal a group of claudin-low cell lines that is distinct from nonmalignant, basal, and luminal lines. The claudin-low cell lines express F11R, EPCAM, and other proteins at very low levels, whereas CD44 is expressed at a high level. Comparison of mRNA expression to glycoprotein expression shows modest correlation; the best agreement occurs when the mRNA expression level is lowest and little or no protein is detected. These findings from cell lines are compared to those for tumor samples by the Clinical Proteomic Tumor Analysis Consortium (CPTAC). The CPTAC samples contain a group low in CLDN3. The samples low in CLDN3 proteins share many differentially expressed glycoproteins with the claudin-low cell lines. In contrast to the situation for cell lines or patient samples classified as claudin-low by RNA expression, however, most of the tumor samples low in CLDN3 protein express the estrogen receptor or HER2. These tumor samples express CD44 protein at low rather than high levels. There is no correlation between CLDN3 gene expression and protein expression in these CPTAC samples; hence, the claudin-low subtype defined by gene expression is not the same group of tumors as that defined by low expression of CLDN3 protein.</description><subject>Biomarkers, Tumor - biosynthesis</subject><subject>Biomarkers, Tumor - genetics</subject><subject>breast neoplasms</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>breasts</subject><subject>Cell Line, Tumor</subject><subject>cell lines</subject><subject>Claudin-3 - biosynthesis</subject><subject>Claudin-3 - genetics</subject><subject>epithelium</subject><subject>estrogen receptors</subject><subject>Female</subject><subject>gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>genes</subject><subject>glycoproteins</subject><subject>Glycoproteins - biosynthesis</subject><subject>Glycoproteins - genetics</subject><subject>Humans</subject><subject>Hyaluronan Receptors - biosynthesis</subject><subject>Hyaluronan Receptors - genetics</subject><subject>liquid chromatography</subject><subject>Mass Spectrometry - methods</subject><subject>messenger RNA</subject><subject>patients</subject><subject>Prognosis</subject><subject>protein synthesis</subject><subject>proteome</subject><subject>Proteomics</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>tandem mass spectrometry</subject><subject>tight junctions</subject><issn>1535-3893</issn><issn>1535-3907</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUha0K1JaBRwB5ySZT_8R2ZoMEUWkrjVQWlK1149yAq4w92ElL3x7TmY7oqivb8neO7rmHkPecLTkT_AxcXt5uU5wwbnCpO8Zqw47IKVdSVXLFzKune7OSJ-RNzreMcWWYPCYnohGNEVqdkh8X44OLjz4-ZOoDbUeYex-qdbynXxJCnmgLwWGiLY4jXfuAmV7CHVKgN8H_npGe_9kmzNnHQL-lOPgR35LXA4wZ3-3PBbn5ev69vazW1xdX7ed1BXWjp6oG6MwKe5C9bhzTkgH2DAanur7jHDRzKLQbjBRdr5SoUUJ5clgVFs0gF-TTznc7dxvsHYYpwWi3yW8gPdgI3j7_Cf6X_RnvrFLK1GU_C_Jxb5BiiZInu_HZlaAQMM7ZCqaNqBvOzIsob4xuuNKaFVTtUJdizgmHw0Sc2X_12VKfPdRn9_UV3Yf_4xxUT30VgO-AR32cUyjbfcH0L-ExrR0</recordid><startdate>20170407</startdate><enddate>20170407</enddate><creator>Yen, Ten-Yang</creator><creator>Bowen, Spencer</creator><creator>Yen, Roger</creator><creator>Piryatinska, Alexandra</creator><creator>Macher, Bruce A</creator><creator>Timpe, Leslie C</creator><general>American Chemical Society</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><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2398-4765</orcidid></search><sort><creationdate>20170407</creationdate><title>Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile</title><author>Yen, Ten-Yang ; Bowen, Spencer ; Yen, Roger ; Piryatinska, Alexandra ; Macher, Bruce A ; Timpe, Leslie C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a486t-4aab79eda3d68c0630aed0afc5bdb11a60ce26cf732bd5524e3a6cf1a9063e7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biomarkers, Tumor - biosynthesis</topic><topic>Biomarkers, Tumor - genetics</topic><topic>breast neoplasms</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>breasts</topic><topic>Cell Line, Tumor</topic><topic>cell lines</topic><topic>Claudin-3 - biosynthesis</topic><topic>Claudin-3 - genetics</topic><topic>epithelium</topic><topic>estrogen receptors</topic><topic>Female</topic><topic>gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>genes</topic><topic>glycoproteins</topic><topic>Glycoproteins - biosynthesis</topic><topic>Glycoproteins - genetics</topic><topic>Humans</topic><topic>Hyaluronan Receptors - biosynthesis</topic><topic>Hyaluronan Receptors - genetics</topic><topic>liquid chromatography</topic><topic>Mass Spectrometry - methods</topic><topic>messenger RNA</topic><topic>patients</topic><topic>Prognosis</topic><topic>protein synthesis</topic><topic>proteome</topic><topic>Proteomics</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>tandem mass spectrometry</topic><topic>tight junctions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yen, Ten-Yang</creatorcontrib><creatorcontrib>Bowen, Spencer</creatorcontrib><creatorcontrib>Yen, Roger</creatorcontrib><creatorcontrib>Piryatinska, Alexandra</creatorcontrib><creatorcontrib>Macher, Bruce A</creatorcontrib><creatorcontrib>Timpe, Leslie C</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><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yen, Ten-Yang</au><au>Bowen, Spencer</au><au>Yen, Roger</au><au>Piryatinska, Alexandra</au><au>Macher, Bruce A</au><au>Timpe, Leslie C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2017-04-07</date><risdate>2017</risdate><volume>16</volume><issue>4</issue><spage>1391</spage><epage>1400</epage><pages>1391-1400</pages><issn>1535-3893</issn><issn>1535-3907</issn><eissn>1535-3907</eissn><abstract>Claudin proteins are components of epithelial tight junctions; a subtype of breast cancer has been defined by the reduced expression of mRNA for claudins and other genes. Here, we characterize the expression of glycoproteins in breast cell lines for the claudin-low subtype using liquid chromatography/tandem mass spectrometry. Unsupervised clustering techniques reveal a group of claudin-low cell lines that is distinct from nonmalignant, basal, and luminal lines. The claudin-low cell lines express F11R, EPCAM, and other proteins at very low levels, whereas CD44 is expressed at a high level. Comparison of mRNA expression to glycoprotein expression shows modest correlation; the best agreement occurs when the mRNA expression level is lowest and little or no protein is detected. These findings from cell lines are compared to those for tumor samples by the Clinical Proteomic Tumor Analysis Consortium (CPTAC). The CPTAC samples contain a group low in CLDN3. The samples low in CLDN3 proteins share many differentially expressed glycoproteins with the claudin-low cell lines. In contrast to the situation for cell lines or patient samples classified as claudin-low by RNA expression, however, most of the tumor samples low in CLDN3 protein express the estrogen receptor or HER2. These tumor samples express CD44 protein at low rather than high levels. There is no correlation between CLDN3 gene expression and protein expression in these CPTAC samples; hence, the claudin-low subtype defined by gene expression is not the same group of tumors as that defined by low expression of CLDN3 protein.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>28287265</pmid><doi>10.1021/acs.jproteome.6b00470</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2398-4765</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers, Tumor - biosynthesis Biomarkers, Tumor - genetics breast neoplasms Breast Neoplasms - genetics Breast Neoplasms - pathology breasts Cell Line, Tumor cell lines Claudin-3 - biosynthesis Claudin-3 - genetics epithelium estrogen receptors Female gene expression Gene Expression Regulation, Neoplastic genes glycoproteins Glycoproteins - biosynthesis Glycoproteins - genetics Humans Hyaluronan Receptors - biosynthesis Hyaluronan Receptors - genetics liquid chromatography Mass Spectrometry - methods messenger RNA patients Prognosis protein synthesis proteome Proteomics Receptor, ErbB-2 - biosynthesis Receptor, ErbB-2 - genetics tandem mass spectrometry tight junctions |
title | Glycoproteins in Claudin-Low Breast Cancer Cell Lines Have a Unique Expression Profile |
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