Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells
Background: Osteopontin (OPN) is a secreted glycoprotein that mediates cell-matrix interactions and cellular signaling by binding with integrin (primarily αvβ3) and CD44 receptors. OPN regulates cell adhesion, chemotaxis, macrophage-directed IL-10 suppression, stressdependent angiogenesis, apoptosis...
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Format: | Article |
Language: | English |
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Elsevier
2007-09-01
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Series: | Neoplasia: An International Journal for Oncology Research |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1476558607800297 |
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author | Chengjiang Gao Zhiyong Mi Hongtao Guo Paul C. Kuo |
author_facet | Chengjiang Gao Zhiyong Mi Hongtao Guo Paul C. Kuo |
author_sort | Chengjiang Gao |
collection | DOAJ |
description | Background: Osteopontin (OPN) is a secreted glycoprotein that mediates cell-matrix interactions and cellular signaling by binding with integrin (primarily αvβ3) and CD44 receptors. OPN regulates cell adhesion, chemotaxis, macrophage-directed IL-10 suppression, stressdependent angiogenesis, apoptosis prevention, anchorage-independent growth of tumor cells. However, the molecular mechanisms that define the role of OPN in tumor progression and metastasis are incompletely understood. Methods: In this study, we use a system of 4T1 and 4T07 murine mammary epithelial tumor cell lines that are divergent in both metastatic phenotype and OPN expression. 4T1 expresses OPN and hematogeneously metastasizes, whereas 4T07 does not express OPN and is highly tumorigenic but fails to metastasize. Results: Our results demonstrate that OPN regulates Stati protein degradation through the ubiquitin-proteasome pathway to alter interferon-γ-dependent growth inhibition and p21 expression. We identify Stat-interacting LIM protein as the critical Stat ubiquitin E3 ligase in this setting. Conclusions: OPN regulates Stati-dependent functions, such as growth inhibition and p21 expression, in the murine mammary epithelial cells lines 4T1 and 4T07. This relationship between OPN and Stati in the context of tumor biology has not been previously examined. |
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format | Article |
id | doaj.art-84f844164eef4d50b83b10f8003323b7 |
institution | Directory Open Access Journal |
issn | 1476-5586 1522-8002 |
language | English |
last_indexed | 2024-12-18T14:27:40Z |
publishDate | 2007-09-01 |
publisher | Elsevier |
record_format | Article |
series | Neoplasia: An International Journal for Oncology Research |
spelling | doaj.art-84f844164eef4d50b83b10f8003323b72022-12-21T21:04:40ZengElsevierNeoplasia: An International Journal for Oncology Research1476-55861522-80022007-09-019969970610.1593/neo.07463Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor CellsChengjiang GaoZhiyong MiHongtao GuoPaul C. KuoBackground: Osteopontin (OPN) is a secreted glycoprotein that mediates cell-matrix interactions and cellular signaling by binding with integrin (primarily αvβ3) and CD44 receptors. OPN regulates cell adhesion, chemotaxis, macrophage-directed IL-10 suppression, stressdependent angiogenesis, apoptosis prevention, anchorage-independent growth of tumor cells. However, the molecular mechanisms that define the role of OPN in tumor progression and metastasis are incompletely understood. Methods: In this study, we use a system of 4T1 and 4T07 murine mammary epithelial tumor cell lines that are divergent in both metastatic phenotype and OPN expression. 4T1 expresses OPN and hematogeneously metastasizes, whereas 4T07 does not express OPN and is highly tumorigenic but fails to metastasize. Results: Our results demonstrate that OPN regulates Stati protein degradation through the ubiquitin-proteasome pathway to alter interferon-γ-dependent growth inhibition and p21 expression. We identify Stat-interacting LIM protein as the critical Stat ubiquitin E3 ligase in this setting. Conclusions: OPN regulates Stati-dependent functions, such as growth inhibition and p21 expression, in the murine mammary epithelial cells lines 4T1 and 4T07. This relationship between OPN and Stati in the context of tumor biology has not been previously examined.http://www.sciencedirect.com/science/article/pii/S1476558607800297UbiquitinSLIMproteasomep21interferon |
spellingShingle | Chengjiang Gao Zhiyong Mi Hongtao Guo Paul C. Kuo Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells Neoplasia: An International Journal for Oncology Research Ubiquitin SLIM proteasome p21 interferon |
title | Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells |
title_full | Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells |
title_fullStr | Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells |
title_full_unstemmed | Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells |
title_short | Osteopontin Regulates Ubiquitin-Dependent Degradation of Stat1 in Murine Mammary Epithelial Tumor Cells |
title_sort | osteopontin regulates ubiquitin dependent degradation of stat1 in murine mammary epithelial tumor cells |
topic | Ubiquitin SLIM proteasome p21 interferon |
url | http://www.sciencedirect.com/science/article/pii/S1476558607800297 |
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