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Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells
PURPOSE: Oxaliplatin is a third-generation platinum compound, and it has no nephrotoxicity and has reduced bone marrow toxicity. Cancer cells that are resistant to cisplatin are sensitive to oxaliplatin. Oxaliplatin is used widely for the treatment of colon cancers. Recently, oxaliplatin was reporte...
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Formato: | Texto |
Lenguaje: | English |
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The Korean Society of Coloproctology
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998014/ https://www.ncbi.nlm.nih.gov/pubmed/21152225 http://dx.doi.org/10.3393/jksc.2010.26.4.246 |
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author | Sohn, Won Jun Lee, Jung Won Park, Dong-Guk |
author_facet | Sohn, Won Jun Lee, Jung Won Park, Dong-Guk |
author_sort | Sohn, Won Jun |
collection | PubMed |
description | PURPOSE: Oxaliplatin is a third-generation platinum compound, and it has no nephrotoxicity and has reduced bone marrow toxicity. Cancer cells that are resistant to cisplatin are sensitive to oxaliplatin. Oxaliplatin is used widely for the treatment of colon cancers. Recently, oxaliplatin was reported to inhibit the expression of survivin, which protects cell apoptosis. However, there are no reports on the expressions of survivin variants and the changes in intracellular localization of survivin in cancer cells. We studied the expression of survivin caused by oxaliplatin in HCT116 colon cancer cells, and we observed the localization of survivin in the mitotic phase. METHODS: We treated the HCT116 colon cancer cells with 2.0 µM of oxaliplatin, and we studied the expressions of survivin protein, and survivin mRNA variants, as well as the changes in intracellular localization, by using the Western blot method, RT-PCR, immunocytochemistry, and flowcytometry. RESULTS: Oxaliplatin inhibits the expression of the survivin protein and survivin mRNA in HCT116 colon cancer cells. The expression of the survivin-2B variants, which have no antiapoptotic activity but control cell mitosis by localization on a microtubule, is reduced continuously 2 days after treatment with oxaliplatin. In immunocytochemistry, expression of survivin in the cytoplasm is reduced and especially is not expressed in microtubules and contractile rings. CONCLUSION: One of the mechanisms of oxaliplatin is to inhibit the expression of and to change the localization of survivin. Based on these results, we suggest that changes in the expression of survivin variants and in their localization are two effects of oxaliplatin. |
format | Text |
id | pubmed-2998014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Society of Coloproctology |
record_format | MEDLINE/PubMed |
spelling | pubmed-29980142010-12-09 Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells Sohn, Won Jun Lee, Jung Won Park, Dong-Guk J Korean Soc Coloproctology Original Article PURPOSE: Oxaliplatin is a third-generation platinum compound, and it has no nephrotoxicity and has reduced bone marrow toxicity. Cancer cells that are resistant to cisplatin are sensitive to oxaliplatin. Oxaliplatin is used widely for the treatment of colon cancers. Recently, oxaliplatin was reported to inhibit the expression of survivin, which protects cell apoptosis. However, there are no reports on the expressions of survivin variants and the changes in intracellular localization of survivin in cancer cells. We studied the expression of survivin caused by oxaliplatin in HCT116 colon cancer cells, and we observed the localization of survivin in the mitotic phase. METHODS: We treated the HCT116 colon cancer cells with 2.0 µM of oxaliplatin, and we studied the expressions of survivin protein, and survivin mRNA variants, as well as the changes in intracellular localization, by using the Western blot method, RT-PCR, immunocytochemistry, and flowcytometry. RESULTS: Oxaliplatin inhibits the expression of the survivin protein and survivin mRNA in HCT116 colon cancer cells. The expression of the survivin-2B variants, which have no antiapoptotic activity but control cell mitosis by localization on a microtubule, is reduced continuously 2 days after treatment with oxaliplatin. In immunocytochemistry, expression of survivin in the cytoplasm is reduced and especially is not expressed in microtubules and contractile rings. CONCLUSION: One of the mechanisms of oxaliplatin is to inhibit the expression of and to change the localization of survivin. Based on these results, we suggest that changes in the expression of survivin variants and in their localization are two effects of oxaliplatin. The Korean Society of Coloproctology 2010-08 2010-08-31 /pmc/articles/PMC2998014/ /pubmed/21152225 http://dx.doi.org/10.3393/jksc.2010.26.4.246 Text en © 2010 The Korean Society of Coloproctology http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sohn, Won Jun Lee, Jung Won Park, Dong-Guk Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title | Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title_full | Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title_fullStr | Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title_full_unstemmed | Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title_short | Change in Expression of Survivin Caused by Using Oxaliplatin in HCT116 Colon Cancer Cells |
title_sort | change in expression of survivin caused by using oxaliplatin in hct116 colon cancer cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998014/ https://www.ncbi.nlm.nih.gov/pubmed/21152225 http://dx.doi.org/10.3393/jksc.2010.26.4.246 |
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