VAMP-associated protein B (VAPB) promotes breast tumor growth by modulation of Akt activity
VAPB (VAMP- associated protein B) is an ER protein that regulates multiple biological functions. Although aberrant expression of VAPB is associated with breast cancer, its function in tumor cells is poorly understood. In this report, we provide evidence that VAPB regulates breast tumor cell prolifer...
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description | VAPB (VAMP- associated protein B) is an ER protein that regulates multiple biological functions. Although aberrant expression of VAPB is associated with breast cancer, its function in tumor cells is poorly understood. In this report, we provide evidence that VAPB regulates breast tumor cell proliferation and AKT activation. VAPB protein expression is elevated in primary and metastatic tumor specimens, and VAPB mRNA expression levels correlated negatively with patient survival in two large breast tumor datasets. Overexpression of VAPB in mammary epithelial cells increased cell growth, whereas VAPB knockdown in tumor cells inhibited cell proliferation in vitro and suppressed tumor growth in orthotopic mammary gland allografts. The growth regulation of mammary tumor cells controlled by VAPB appears to be mediated, at least in part, by modulation of AKT activity. Overexpression of VAPB in MCF10A-HER2 cells enhances phosphorylation of AKT. In contrast, knockdown of VAPB in MMTV-Neu tumor cells inhibited pAKT levels. Pharmacological inhibition of AKT significantly reduced three-dimensional spheroid growth induced by VAPB. Collectively, the genetic, functional and mechanistic analyses suggest a role of VAPB in tumor promotion in human breast cancer. |
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Although aberrant expression of VAPB is associated with breast cancer, its function in tumor cells is poorly understood. In this report, we provide evidence that VAPB regulates breast tumor cell proliferation and AKT activation. VAPB protein expression is elevated in primary and metastatic tumor specimens, and VAPB mRNA expression levels correlated negatively with patient survival in two large breast tumor datasets. Overexpression of VAPB in mammary epithelial cells increased cell growth, whereas VAPB knockdown in tumor cells inhibited cell proliferation in vitro and suppressed tumor growth in orthotopic mammary gland allografts. The growth regulation of mammary tumor cells controlled by VAPB appears to be mediated, at least in part, by modulation of AKT activity. Overexpression of VAPB in MCF10A-HER2 cells enhances phosphorylation of AKT. In contrast, knockdown of VAPB in MMTV-Neu tumor cells inhibited pAKT levels. Pharmacological inhibition of AKT significantly reduced three-dimensional spheroid growth induced by VAPB. Collectively, the genetic, functional and mechanistic analyses suggest a role of VAPB in tumor promotion in human breast cancer.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0046281</identifier><identifier>PMID: 23049696</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aberration ; AKT protein ; Allografts ; Amyotrophic lateral sclerosis ; Analysis ; Analysis of Variance ; Animals ; Apoptosis ; Binding sites ; Biology ; Breast cancer ; Breast Neoplasms - metabolism ; Breast Neoplasms - physiopathology ; Cancer ; Cancer metastasis ; Cancer treatment ; Cell activation ; Cell growth ; Cell Line, Tumor ; Cell Proliferation ; Datasets ; Endoplasmic reticulum ; Enzyme Activation - physiology ; Epithelial cells ; ErbB-2 protein ; Female ; Gene expression ; Gene Expression Profiling ; Genomes ; Growth ; Growth factors ; Humans ; Immunoblotting ; Immunohistochemistry ; Inhibition ; Kinases ; Ligands ; Lipids ; Mammary gland ; Medicine ; Metastases ; Mice ; Microarray Analysis ; Modulation ; Mutation ; Oncogene Protein v-akt - metabolism ; Pharmacology ; Phosphorylation ; Physicians ; Plasmids ; Plasmids - genetics ; Protein B ; Proteins ; RNA ; Rodents ; Spheroids, Cellular - cytology ; Survival Analysis ; Tumor cells ; Tumors ; Vesicular Transport Proteins - metabolism ; Virulence-associated protein B</subject><ispartof>PloS one, 2012-10, Vol.7 (10), p.e46281-e46281</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Rao et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Rao et al 2012 Rao et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-cecfbf3d48a8e8b7a4d658e103f58a3761992ec500c780929b70a43cd43b06a53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462209/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462209/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23870,27928,27929,53795,53797</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23049696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Debinski, Waldemar</contributor><creatorcontrib>Rao, Meghana</creatorcontrib><creatorcontrib>Song, Wenqiang</creatorcontrib><creatorcontrib>Jiang, Aixiang</creatorcontrib><creatorcontrib>Shyr, Yu</creatorcontrib><creatorcontrib>Lev, Sima</creatorcontrib><creatorcontrib>Greenstein, David</creatorcontrib><creatorcontrib>Brantley-Sieders, Dana</creatorcontrib><creatorcontrib>Chen, Jin</creatorcontrib><title>VAMP-associated protein B (VAPB) promotes breast tumor growth by modulation of Akt activity</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>VAPB (VAMP- associated protein B) is an ER protein that regulates multiple biological functions. Although aberrant expression of VAPB is associated with breast cancer, its function in tumor cells is poorly understood. In this report, we provide evidence that VAPB regulates breast tumor cell proliferation and AKT activation. VAPB protein expression is elevated in primary and metastatic tumor specimens, and VAPB mRNA expression levels correlated negatively with patient survival in two large breast tumor datasets. Overexpression of VAPB in mammary epithelial cells increased cell growth, whereas VAPB knockdown in tumor cells inhibited cell proliferation in vitro and suppressed tumor growth in orthotopic mammary gland allografts. The growth regulation of mammary tumor cells controlled by VAPB appears to be mediated, at least in part, by modulation of AKT activity. Overexpression of VAPB in MCF10A-HER2 cells enhances phosphorylation of AKT. In contrast, knockdown of VAPB in MMTV-Neu tumor cells inhibited pAKT levels. Pharmacological inhibition of AKT significantly reduced three-dimensional spheroid growth induced by VAPB. Collectively, the genetic, functional and mechanistic analyses suggest a role of VAPB in tumor promotion in human breast cancer.</description><subject>Aberration</subject><subject>AKT protein</subject><subject>Allografts</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Analysis</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Binding sites</subject><subject>Biology</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - physiopathology</subject><subject>Cancer</subject><subject>Cancer metastasis</subject><subject>Cancer treatment</subject><subject>Cell activation</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Datasets</subject><subject>Endoplasmic reticulum</subject><subject>Enzyme Activation - physiology</subject><subject>Epithelial cells</subject><subject>ErbB-2 protein</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Genomes</subject><subject>Growth</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>Inhibition</subject><subject>Kinases</subject><subject>Ligands</subject><subject>Lipids</subject><subject>Mammary gland</subject><subject>Medicine</subject><subject>Metastases</subject><subject>Mice</subject><subject>Microarray Analysis</subject><subject>Modulation</subject><subject>Mutation</subject><subject>Oncogene Protein v-akt - metabolism</subject><subject>Pharmacology</subject><subject>Phosphorylation</subject><subject>Physicians</subject><subject>Plasmids</subject><subject>Plasmids - genetics</subject><subject>Protein B</subject><subject>Proteins</subject><subject>RNA</subject><subject>Rodents</subject><subject>Spheroids, Cellular - cytology</subject><subject>Survival Analysis</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>Vesicular Transport Proteins - metabolism</subject><subject>Virulence-associated protein B</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAUjBCIloV_gMASl3LIYscfsS-V0oqPSkX0AL1wsGzH2XpJ4sV2ivbf42XTqosqH2yNZ-b5PU9RvEZwiXCNPqz9FEbVLzd-tEsICas4elIcI4GrklUQP31wPipexLiGkGLO2PPiqMKQCCbYcfHzuvl6VaoYvXEq2RZsgk_WjeAMnFw3V2fvd8CQoQh0sComkKbBB7AK_k-6AXoLBt9OvUrOj8B3oPmVgDLJ3bq0fVk861Qf7at5XxQ_Pn38fv6lvPz2-eK8uSwNoyKVxppOd7glXHHLda1Iyyi3COKOcoVrhoSorKEQmppDUQldQ0WwaQnWkCmKF8Xbve-m91HOc4kSYUJodkE7xsWe0Xq1lpvgBhW20isn_wE-rKQKyZneSkMo40TwmlpGiK41JRprwgnBRNk8y0VxOleb9GBbY8cUVH9gengzuhu58rcS5y-qoMgGJ7NB8L8nG5McXDS279Vo_ZTfDQXlqKpqlKnv_qM-3t3MWqncgBs7n-uanalsKMEYCcZwZi0fYeXV2sGZHKLOZfxAQPYCE3yMwXb3PSIodxG8e4zcRVDOEcyyNw_ncy-6yxz-C1hy1uk</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Rao, Meghana</creator><creator>Song, Wenqiang</creator><creator>Jiang, Aixiang</creator><creator>Shyr, Yu</creator><creator>Lev, Sima</creator><creator>Greenstein, David</creator><creator>Brantley-Sieders, Dana</creator><creator>Chen, Jin</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20121001</creationdate><title>VAMP-associated protein B (VAPB) promotes breast tumor growth by modulation of Akt activity</title><author>Rao, Meghana ; Song, Wenqiang ; Jiang, Aixiang ; Shyr, Yu ; Lev, Sima ; Greenstein, David ; Brantley-Sieders, Dana ; Chen, Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c659t-cecfbf3d48a8e8b7a4d658e103f58a3761992ec500c780929b70a43cd43b06a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aberration</topic><topic>AKT protein</topic><topic>Allografts</topic><topic>Amyotrophic lateral sclerosis</topic><topic>Analysis</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Binding sites</topic><topic>Biology</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - physiopathology</topic><topic>Cancer</topic><topic>Cancer metastasis</topic><topic>Cancer treatment</topic><topic>Cell activation</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Datasets</topic><topic>Endoplasmic reticulum</topic><topic>Enzyme Activation - physiology</topic><topic>Epithelial cells</topic><topic>ErbB-2 protein</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Genomes</topic><topic>Growth</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>Inhibition</topic><topic>Kinases</topic><topic>Ligands</topic><topic>Lipids</topic><topic>Mammary gland</topic><topic>Medicine</topic><topic>Metastases</topic><topic>Mice</topic><topic>Microarray Analysis</topic><topic>Modulation</topic><topic>Mutation</topic><topic>Oncogene Protein v-akt - metabolism</topic><topic>Pharmacology</topic><topic>Phosphorylation</topic><topic>Physicians</topic><topic>Plasmids</topic><topic>Plasmids - 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Although aberrant expression of VAPB is associated with breast cancer, its function in tumor cells is poorly understood. In this report, we provide evidence that VAPB regulates breast tumor cell proliferation and AKT activation. VAPB protein expression is elevated in primary and metastatic tumor specimens, and VAPB mRNA expression levels correlated negatively with patient survival in two large breast tumor datasets. Overexpression of VAPB in mammary epithelial cells increased cell growth, whereas VAPB knockdown in tumor cells inhibited cell proliferation in vitro and suppressed tumor growth in orthotopic mammary gland allografts. The growth regulation of mammary tumor cells controlled by VAPB appears to be mediated, at least in part, by modulation of AKT activity. Overexpression of VAPB in MCF10A-HER2 cells enhances phosphorylation of AKT. In contrast, knockdown of VAPB in MMTV-Neu tumor cells inhibited pAKT levels. Pharmacological inhibition of AKT significantly reduced three-dimensional spheroid growth induced by VAPB. Collectively, the genetic, functional and mechanistic analyses suggest a role of VAPB in tumor promotion in human breast cancer.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23049696</pmid><doi>10.1371/journal.pone.0046281</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aberration AKT protein Allografts Amyotrophic lateral sclerosis Analysis Analysis of Variance Animals Apoptosis Binding sites Biology Breast cancer Breast Neoplasms - metabolism Breast Neoplasms - physiopathology Cancer Cancer metastasis Cancer treatment Cell activation Cell growth Cell Line, Tumor Cell Proliferation Datasets Endoplasmic reticulum Enzyme Activation - physiology Epithelial cells ErbB-2 protein Female Gene expression Gene Expression Profiling Genomes Growth Growth factors Humans Immunoblotting Immunohistochemistry Inhibition Kinases Ligands Lipids Mammary gland Medicine Metastases Mice Microarray Analysis Modulation Mutation Oncogene Protein v-akt - metabolism Pharmacology Phosphorylation Physicians Plasmids Plasmids - genetics Protein B Proteins RNA Rodents Spheroids, Cellular - cytology Survival Analysis Tumor cells Tumors Vesicular Transport Proteins - metabolism Virulence-associated protein B |
title | VAMP-associated protein B (VAPB) promotes breast tumor growth by modulation of Akt activity |
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