author_facet Stürzl, Michael
Gaus, Dominika
Dirks, Wilhelm G.
Ganem, Don
Jochmann, Ramona
Stürzl, Michael
Gaus, Dominika
Dirks, Wilhelm G.
Ganem, Don
Jochmann, Ramona
author Stürzl, Michael
Gaus, Dominika
Dirks, Wilhelm G.
Ganem, Don
Jochmann, Ramona
spellingShingle Stürzl, Michael
Gaus, Dominika
Dirks, Wilhelm G.
Ganem, Don
Jochmann, Ramona
International Journal of Cancer
Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
Cancer Research
Oncology
author_sort stürzl, michael
spelling Stürzl, Michael Gaus, Dominika Dirks, Wilhelm G. Ganem, Don Jochmann, Ramona 0020-7136 1097-0215 Wiley Cancer Research Oncology http://dx.doi.org/10.1002/ijc.27849 <jats:title>Abstract</jats:title><jats:p>Kaposi's sarcoma (KS) is an endothelial cell‐derived tumor. Investigations of the molecular mechanisms of KS pathogenesis and the identification of drugs for treatment of KS depend critically on valid cell‐culture models. Two major immortalized cell lines are available for KS research. Recently, the KS cell line KS Y‐1 has been shown to be cross‐contaminated with the T24 urinary bladder cancer cell line (ATCC HTB‐4). Here, we show by short tandem repeat profiling that the second KS cell line, SLK, is indistinguishable from the clear‐cell renal‐cell carcinoma cell line Caki‐1. Immunocytochemical detection of cytokeratin expression confirmed the epithelial‐cell origin of SLK cells. Our findings indicate that SLK cells are not of endothelial origin and should not be used in future studies as a model for KS‐derived endothelial tumor cells. We suggest that in the future, more attention needs to be paid to the authenticity of cells in lines derived from human tissues.</jats:p> Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line International Journal of Cancer
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series International Journal of Cancer
source_id 49
title Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_unstemmed Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_full Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_fullStr Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_full_unstemmed Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_short Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_sort kaposi's sarcoma‐derived cell line slk is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
topic Cancer Research
Oncology
url http://dx.doi.org/10.1002/ijc.27849
publishDate 2013
physical 1954-1958
description <jats:title>Abstract</jats:title><jats:p>Kaposi's sarcoma (KS) is an endothelial cell‐derived tumor. Investigations of the molecular mechanisms of KS pathogenesis and the identification of drugs for treatment of KS depend critically on valid cell‐culture models. Two major immortalized cell lines are available for KS research. Recently, the KS cell line KS Y‐1 has been shown to be cross‐contaminated with the T24 urinary bladder cancer cell line (ATCC HTB‐4). Here, we show by short tandem repeat profiling that the second KS cell line, SLK, is indistinguishable from the clear‐cell renal‐cell carcinoma cell line Caki‐1. Immunocytochemical detection of cytokeratin expression confirmed the epithelial‐cell origin of SLK cells. Our findings indicate that SLK cells are not of endothelial origin and should not be used in future studies as a model for KS‐derived endothelial tumor cells. We suggest that in the future, more attention needs to be paid to the authenticity of cells in lines derived from human tissues.</jats:p>
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author Stürzl, Michael, Gaus, Dominika, Dirks, Wilhelm G., Ganem, Don, Jochmann, Ramona
author_facet Stürzl, Michael, Gaus, Dominika, Dirks, Wilhelm G., Ganem, Don, Jochmann, Ramona, Stürzl, Michael, Gaus, Dominika, Dirks, Wilhelm G., Ganem, Don, Jochmann, Ramona
author_sort stürzl, michael
container_issue 8
container_start_page 1954
container_title International Journal of Cancer
container_volume 132
description <jats:title>Abstract</jats:title><jats:p>Kaposi's sarcoma (KS) is an endothelial cell‐derived tumor. Investigations of the molecular mechanisms of KS pathogenesis and the identification of drugs for treatment of KS depend critically on valid cell‐culture models. Two major immortalized cell lines are available for KS research. Recently, the KS cell line KS Y‐1 has been shown to be cross‐contaminated with the T24 urinary bladder cancer cell line (ATCC HTB‐4). Here, we show by short tandem repeat profiling that the second KS cell line, SLK, is indistinguishable from the clear‐cell renal‐cell carcinoma cell line Caki‐1. Immunocytochemical detection of cytokeratin expression confirmed the epithelial‐cell origin of SLK cells. Our findings indicate that SLK cells are not of endothelial origin and should not be used in future studies as a model for KS‐derived endothelial tumor cells. We suggest that in the future, more attention needs to be paid to the authenticity of cells in lines derived from human tissues.</jats:p>
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spelling Stürzl, Michael Gaus, Dominika Dirks, Wilhelm G. Ganem, Don Jochmann, Ramona 0020-7136 1097-0215 Wiley Cancer Research Oncology http://dx.doi.org/10.1002/ijc.27849 <jats:title>Abstract</jats:title><jats:p>Kaposi's sarcoma (KS) is an endothelial cell‐derived tumor. Investigations of the molecular mechanisms of KS pathogenesis and the identification of drugs for treatment of KS depend critically on valid cell‐culture models. Two major immortalized cell lines are available for KS research. Recently, the KS cell line KS Y‐1 has been shown to be cross‐contaminated with the T24 urinary bladder cancer cell line (ATCC HTB‐4). Here, we show by short tandem repeat profiling that the second KS cell line, SLK, is indistinguishable from the clear‐cell renal‐cell carcinoma cell line Caki‐1. Immunocytochemical detection of cytokeratin expression confirmed the epithelial‐cell origin of SLK cells. Our findings indicate that SLK cells are not of endothelial origin and should not be used in future studies as a model for KS‐derived endothelial tumor cells. We suggest that in the future, more attention needs to be paid to the authenticity of cells in lines derived from human tissues.</jats:p> Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line International Journal of Cancer
spellingShingle Stürzl, Michael, Gaus, Dominika, Dirks, Wilhelm G., Ganem, Don, Jochmann, Ramona, International Journal of Cancer, Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line, Cancer Research, Oncology
title Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_full Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_fullStr Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_full_unstemmed Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_short Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_sort kaposi's sarcoma‐derived cell line slk is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
title_unstemmed Kaposi's sarcoma‐derived cell line SLK is not of endothelial origin, but is a contaminant from a known renal carcinoma cell line
topic Cancer Research, Oncology
url http://dx.doi.org/10.1002/ijc.27849