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Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells

Brazilin, isolated from the methanol extract of the heart wood of Caesalpinia sappan, sensitizes cancer cells to apoptosis. Glioblastoma multiforme (GBM), which accounts for most cases of central nervous system malignancy, has a very poor prognosis and lacks effective therapeutic interventions. We,...

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Detalles Bibliográficos
Autores principales: Lee, Dae-Young, Lee, Mi-Kyoung, Kim, Geum-Soog, Noh, Hyung-Jun, Lee, Min-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270480/
https://www.ncbi.nlm.nih.gov/pubmed/23429418
http://dx.doi.org/10.3390/molecules18022449
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author Lee, Dae-Young
Lee, Mi-Kyoung
Kim, Geum-Soog
Noh, Hyung-Jun
Lee, Min-Ho
author_facet Lee, Dae-Young
Lee, Mi-Kyoung
Kim, Geum-Soog
Noh, Hyung-Jun
Lee, Min-Ho
author_sort Lee, Dae-Young
collection PubMed
description Brazilin, isolated from the methanol extract of the heart wood of Caesalpinia sappan, sensitizes cancer cells to apoptosis. Glioblastoma multiforme (GBM), which accounts for most cases of central nervous system malignancy, has a very poor prognosis and lacks effective therapeutic interventions. We, therefore, investigated the effects of different concentrations of and different periods of exposure to brazilin on cell proliferation and apoptosis in the glioma U87 cell line. Cell proliferation was investigated by MTT assays and growth curve analysis, apoptosis was assessed by FACS analysis and western blot studies. Brazilin showed dose-dependent inhibition of cell proliferation and induction of apoptosis in glioma cells. It also increased the ratio of cleaved poly-(ADP)-ribose polymerase and decreased the expression of caspase-3 and caspase-7.
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spelling pubmed-62704802018-12-14 Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells Lee, Dae-Young Lee, Mi-Kyoung Kim, Geum-Soog Noh, Hyung-Jun Lee, Min-Ho Molecules Communication Brazilin, isolated from the methanol extract of the heart wood of Caesalpinia sappan, sensitizes cancer cells to apoptosis. Glioblastoma multiforme (GBM), which accounts for most cases of central nervous system malignancy, has a very poor prognosis and lacks effective therapeutic interventions. We, therefore, investigated the effects of different concentrations of and different periods of exposure to brazilin on cell proliferation and apoptosis in the glioma U87 cell line. Cell proliferation was investigated by MTT assays and growth curve analysis, apoptosis was assessed by FACS analysis and western blot studies. Brazilin showed dose-dependent inhibition of cell proliferation and induction of apoptosis in glioma cells. It also increased the ratio of cleaved poly-(ADP)-ribose polymerase and decreased the expression of caspase-3 and caspase-7. MDPI 2013-02-21 /pmc/articles/PMC6270480/ /pubmed/23429418 http://dx.doi.org/10.3390/molecules18022449 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Lee, Dae-Young
Lee, Mi-Kyoung
Kim, Geum-Soog
Noh, Hyung-Jun
Lee, Min-Ho
Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title_full Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title_fullStr Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title_full_unstemmed Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title_short Brazilin Inhibits Growth and Induces Apoptosis in Human Glioblastoma Cells
title_sort brazilin inhibits growth and induces apoptosis in human glioblastoma cells
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270480/
https://www.ncbi.nlm.nih.gov/pubmed/23429418
http://dx.doi.org/10.3390/molecules18022449
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