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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Veröffentlicht in:PloS one 2012-10, Vol.7 (10), p.e46281-e46281
Hauptverfasser: Rao, Meghana, Song, Wenqiang, Jiang, Aixiang, Shyr, Yu, Lev, Sima, Greenstein, David, Brantley-Sieders, Dana, Chen, Jin
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container_title PloS one
container_volume 7
creator Rao, Meghana
Song, Wenqiang
Jiang, Aixiang
Shyr, Yu
Lev, Sima
Greenstein, David
Brantley-Sieders, Dana
Chen, Jin
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. 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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. 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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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