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Cell Senescence in Myxoid/Round Cell Liposarcoma
Myxoid/round cell liposarcoma (MLS/RCLS) is the second most common liposarcoma type and characterized by the fusion oncogenes FUS-DDIT3 or EWSR1-DDIT3. Previous analysis of cell cycle regulatory proteins revealed a prominent expression of G1-cyclins, cyclin dependent kinases, and their inhibitors bu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095996/ https://www.ncbi.nlm.nih.gov/pubmed/25093008 http://dx.doi.org/10.1155/2014/208786 |
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author | Kåbjörn Gustafsson, Christina Ståhlberg, Anders Engtröm, Katarina Danielsson, Anna Turesson, Ingela Åman, Pierre |
author_facet | Kåbjörn Gustafsson, Christina Ståhlberg, Anders Engtröm, Katarina Danielsson, Anna Turesson, Ingela Åman, Pierre |
author_sort | Kåbjörn Gustafsson, Christina |
collection | PubMed |
description | Myxoid/round cell liposarcoma (MLS/RCLS) is the second most common liposarcoma type and characterized by the fusion oncogenes FUS-DDIT3 or EWSR1-DDIT3. Previous analysis of cell cycle regulatory proteins revealed a prominent expression of G1-cyclins, cyclin dependent kinases, and their inhibitors but very few cells progressing through the G1/S boundary. Here, we extend the investigation to proteins involved in cell senescence in an immunohistochemistry based study of 17 MLS/RCLS cases. Large subpopulations of tumor cells expressed the RBL2 pocket protein and senescence associated heterochromatin 1γ and IL8 receptor β. We conclude that MLS/RCLS tissues contain major populations of senescent tumor cells and this may explain the slow growth rate of this tumor type. |
format | Online Article Text |
id | pubmed-4095996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40959962014-08-04 Cell Senescence in Myxoid/Round Cell Liposarcoma Kåbjörn Gustafsson, Christina Ståhlberg, Anders Engtröm, Katarina Danielsson, Anna Turesson, Ingela Åman, Pierre Sarcoma Research Article Myxoid/round cell liposarcoma (MLS/RCLS) is the second most common liposarcoma type and characterized by the fusion oncogenes FUS-DDIT3 or EWSR1-DDIT3. Previous analysis of cell cycle regulatory proteins revealed a prominent expression of G1-cyclins, cyclin dependent kinases, and their inhibitors but very few cells progressing through the G1/S boundary. Here, we extend the investigation to proteins involved in cell senescence in an immunohistochemistry based study of 17 MLS/RCLS cases. Large subpopulations of tumor cells expressed the RBL2 pocket protein and senescence associated heterochromatin 1γ and IL8 receptor β. We conclude that MLS/RCLS tissues contain major populations of senescent tumor cells and this may explain the slow growth rate of this tumor type. Hindawi Publishing Corporation 2014 2014-06-24 /pmc/articles/PMC4095996/ /pubmed/25093008 http://dx.doi.org/10.1155/2014/208786 Text en Copyright © 2014 Christina Kåbjörn Gustafsson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kåbjörn Gustafsson, Christina Ståhlberg, Anders Engtröm, Katarina Danielsson, Anna Turesson, Ingela Åman, Pierre Cell Senescence in Myxoid/Round Cell Liposarcoma |
title | Cell Senescence in Myxoid/Round Cell Liposarcoma |
title_full | Cell Senescence in Myxoid/Round Cell Liposarcoma |
title_fullStr | Cell Senescence in Myxoid/Round Cell Liposarcoma |
title_full_unstemmed | Cell Senescence in Myxoid/Round Cell Liposarcoma |
title_short | Cell Senescence in Myxoid/Round Cell Liposarcoma |
title_sort | cell senescence in myxoid/round cell liposarcoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095996/ https://www.ncbi.nlm.nih.gov/pubmed/25093008 http://dx.doi.org/10.1155/2014/208786 |
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