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Impaired melanoma growth in VASP deficient mice
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Zeitschriftentitel: | FEBS Letters |
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Personen und Körperschaften: | , , , , |
In: | FEBS Letters, 585, 2011, 15, S. 2533-2536 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Wiley
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Schlagwörter: |
author_facet |
Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas |
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author |
Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas |
spellingShingle |
Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas FEBS Letters Impaired melanoma growth in VASP deficient mice Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics |
author_sort |
kim, young min |
spelling |
Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas 0014-5793 1873-3468 Wiley Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics http://dx.doi.org/10.1016/j.febslet.2011.07.002 <jats:p>Progression of tumors depends on interactions of cancer cells with the host environment. Expression of the cytoskeleton protein VASP is upregulated in various cancer entities. We analyzed the role of VASP for melanoma growth in murine allograft models. Growth of VASP expressing melanomas was retarded in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals. Over time tumor size was <50% in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals and independent of expression levels of Ena/VASP protein family members. Histological analyses showed smaller cells with impaired nutrition status and less vascularization in melanomas derived from VASP<jats:sup>−/−</jats:sup> versus counterparts from wild‐type mice. Cumulatively, the data reveal a critical role of VASP in non‐tumor cells in the tumor environment for melanoma growth in vivo.</jats:p> Impaired melanoma growth in VASP deficient mice FEBS Letters |
doi_str_mv |
10.1016/j.febslet.2011.07.002 |
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Biologie Chemie und Pharmazie Physik |
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Wiley, 2011 |
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Wiley, 2011 |
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2011 |
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Wiley |
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FEBS Letters |
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49 |
title |
Impaired melanoma growth in VASP deficient mice |
title_unstemmed |
Impaired melanoma growth in VASP deficient mice |
title_full |
Impaired melanoma growth in VASP deficient mice |
title_fullStr |
Impaired melanoma growth in VASP deficient mice |
title_full_unstemmed |
Impaired melanoma growth in VASP deficient mice |
title_short |
Impaired melanoma growth in VASP deficient mice |
title_sort |
impaired melanoma growth in vasp deficient mice |
topic |
Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics |
url |
http://dx.doi.org/10.1016/j.febslet.2011.07.002 |
publishDate |
2011 |
physical |
2533-2536 |
description |
<jats:p>Progression of tumors depends on interactions of cancer cells with the host environment. Expression of the cytoskeleton protein VASP is upregulated in various cancer entities. We analyzed the role of VASP for melanoma growth in murine allograft models. Growth of VASP expressing melanomas was retarded in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals. Over time tumor size was <50% in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals and independent of expression levels of Ena/VASP protein family members. Histological analyses showed smaller cells with impaired nutrition status and less vascularization in melanomas derived from VASP<jats:sup>−/−</jats:sup> versus counterparts from wild‐type mice. Cumulatively, the data reveal a critical role of VASP in non‐tumor cells in the tumor environment for melanoma growth in vivo.</jats:p> |
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author | Kim, Young Min, Renné, Christoph, Seifert, Stefanie, Schuh, Kai, Renné, Thomas |
author_facet | Kim, Young Min, Renné, Christoph, Seifert, Stefanie, Schuh, Kai, Renné, Thomas, Kim, Young Min, Renné, Christoph, Seifert, Stefanie, Schuh, Kai, Renné, Thomas |
author_sort | kim, young min |
container_issue | 15 |
container_start_page | 2533 |
container_title | FEBS Letters |
container_volume | 585 |
description | <jats:p>Progression of tumors depends on interactions of cancer cells with the host environment. Expression of the cytoskeleton protein VASP is upregulated in various cancer entities. We analyzed the role of VASP for melanoma growth in murine allograft models. Growth of VASP expressing melanomas was retarded in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals. Over time tumor size was <50% in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals and independent of expression levels of Ena/VASP protein family members. Histological analyses showed smaller cells with impaired nutrition status and less vascularization in melanomas derived from VASP<jats:sup>−/−</jats:sup> versus counterparts from wild‐type mice. Cumulatively, the data reveal a critical role of VASP in non‐tumor cells in the tumor environment for melanoma growth in vivo.</jats:p> |
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imprint | Wiley, 2011 |
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source_id | 49 |
spelling | Kim, Young Min Renné, Christoph Seifert, Stefanie Schuh, Kai Renné, Thomas 0014-5793 1873-3468 Wiley Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics http://dx.doi.org/10.1016/j.febslet.2011.07.002 <jats:p>Progression of tumors depends on interactions of cancer cells with the host environment. Expression of the cytoskeleton protein VASP is upregulated in various cancer entities. We analyzed the role of VASP for melanoma growth in murine allograft models. Growth of VASP expressing melanomas was retarded in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals. Over time tumor size was <50% in VASP<jats:sup>−/−</jats:sup> versus wild‐type animals and independent of expression levels of Ena/VASP protein family members. Histological analyses showed smaller cells with impaired nutrition status and less vascularization in melanomas derived from VASP<jats:sup>−/−</jats:sup> versus counterparts from wild‐type mice. Cumulatively, the data reveal a critical role of VASP in non‐tumor cells in the tumor environment for melanoma growth in vivo.</jats:p> Impaired melanoma growth in VASP deficient mice FEBS Letters |
spellingShingle | Kim, Young Min, Renné, Christoph, Seifert, Stefanie, Schuh, Kai, Renné, Thomas, FEBS Letters, Impaired melanoma growth in VASP deficient mice, Cell Biology, Genetics, Molecular Biology, Biochemistry, Structural Biology, Biophysics |
title | Impaired melanoma growth in VASP deficient mice |
title_full | Impaired melanoma growth in VASP deficient mice |
title_fullStr | Impaired melanoma growth in VASP deficient mice |
title_full_unstemmed | Impaired melanoma growth in VASP deficient mice |
title_short | Impaired melanoma growth in VASP deficient mice |
title_sort | impaired melanoma growth in vasp deficient mice |
title_unstemmed | Impaired melanoma growth in VASP deficient mice |
topic | Cell Biology, Genetics, Molecular Biology, Biochemistry, Structural Biology, Biophysics |
url | http://dx.doi.org/10.1016/j.febslet.2011.07.002 |