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Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol
Betulinic Acid (BetA) and its derivatives have been extensively studied in the past for their anti-tumor effects, but relatively little is known about its precursor Betulin (BE). We found that BE induces apoptosis utilizing a similar mechanism as BetA and is prevented by cyclosporin A (CsA). BE indu...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671171/ https://www.ncbi.nlm.nih.gov/pubmed/19399186 http://dx.doi.org/10.1371/journal.pone.0005361 |
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author | Mullauer, Franziska B. Kessler, Jan H. Medema, Jan Paul |
author_facet | Mullauer, Franziska B. Kessler, Jan H. Medema, Jan Paul |
author_sort | Mullauer, Franziska B. |
collection | PubMed |
description | Betulinic Acid (BetA) and its derivatives have been extensively studied in the past for their anti-tumor effects, but relatively little is known about its precursor Betulin (BE). We found that BE induces apoptosis utilizing a similar mechanism as BetA and is prevented by cyclosporin A (CsA). BE induces cell death more rapidly as compared to BetA, but to achieve similar amounts of cell death a considerably higher concentration of BE is needed. Interestingly, we observed that cholesterol sensitized cells to BE-induced apoptosis, while there was no effect of cholesterol when combined with BetA. Despite the significantly enhanced cytotoxicity, the mode of cell death was not changed as CsA completely abrogated cell death. These results indicate that BE has potent anti-tumor activity especially in combination with cholesterol. |
format | Text |
id | pubmed-2671171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26711712009-04-28 Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol Mullauer, Franziska B. Kessler, Jan H. Medema, Jan Paul PLoS One Research Article Betulinic Acid (BetA) and its derivatives have been extensively studied in the past for their anti-tumor effects, but relatively little is known about its precursor Betulin (BE). We found that BE induces apoptosis utilizing a similar mechanism as BetA and is prevented by cyclosporin A (CsA). BE induces cell death more rapidly as compared to BetA, but to achieve similar amounts of cell death a considerably higher concentration of BE is needed. Interestingly, we observed that cholesterol sensitized cells to BE-induced apoptosis, while there was no effect of cholesterol when combined with BetA. Despite the significantly enhanced cytotoxicity, the mode of cell death was not changed as CsA completely abrogated cell death. These results indicate that BE has potent anti-tumor activity especially in combination with cholesterol. Public Library of Science 2009-04-28 /pmc/articles/PMC2671171/ /pubmed/19399186 http://dx.doi.org/10.1371/journal.pone.0005361 Text en Mullauer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mullauer, Franziska B. Kessler, Jan H. Medema, Jan Paul Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title | Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title_full | Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title_fullStr | Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title_full_unstemmed | Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title_short | Betulin Is a Potent Anti-Tumor Agent that Is Enhanced by Cholesterol |
title_sort | betulin is a potent anti-tumor agent that is enhanced by cholesterol |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671171/ https://www.ncbi.nlm.nih.gov/pubmed/19399186 http://dx.doi.org/10.1371/journal.pone.0005361 |
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