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The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2
The present study investigated the anti-proliferative and chemosensitizing effects of Crinum asiaticum var. japonicum against multi-drug resistant (MDR) cancer cells. The 80% methanol extract, chloroform (CHCI(3)) fraction and butanol (BuOH) fraction of C asiaticum inhibited the growth of mitoxantro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006299/ https://www.ncbi.nlm.nih.gov/pubmed/32038774 http://dx.doi.org/10.5487/TR.2008.24.1.029 |
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author | Hyun, Jae-Hee Kang, Jung-Il Kim, Sang-Cheol Kim, Elvira Kang, Ji-Hoon Kwon, Jung-Mi Park, Doek-Bae Lee, Young-Jae Yoo, Eun-Sook Kang, Hee-Kyoung |
author_facet | Hyun, Jae-Hee Kang, Jung-Il Kim, Sang-Cheol Kim, Elvira Kang, Ji-Hoon Kwon, Jung-Mi Park, Doek-Bae Lee, Young-Jae Yoo, Eun-Sook Kang, Hee-Kyoung |
author_sort | Hyun, Jae-Hee |
collection | PubMed |
description | The present study investigated the anti-proliferative and chemosensitizing effects of Crinum asiaticum var. japonicum against multi-drug resistant (MDR) cancer cells. The 80% methanol extract, chloroform (CHCI(3)) fraction and butanol (BuOH) fraction of C asiaticum inhibited the growth of mitoxantrone (MX) resistant HL-60 (HL-60/MX2) cells. When HL-60/MX2 cells were treated with the CHCI(3) and BuOH fractions, DNA ladder and sub-G1 hypodiploid cells were observed. Furthermore, the fractions reduced Bcl-2 mRNA levels, whereas Bax mRNA levels were increased. These results suggest that the inhibitory effect of C. asiaticum on the growth of the HL-60/MX2 cells might arise from the induction of apoptosis. Treatment of HL-60/MX2 cells with the fractions markedly decreased the mRNA levels of the multi-drug resistance protein-1 and breast cancer resistance protein. The CHCI3 fraction and hexane fraction increased MX accumulation in HL-60/MX2 cells. These results imply that the CHCI(3) fraction of C asiaticum plays a pivotal role as a chemosensitizer. We suggest that components of C asiaticum might have a therapeutic potential for the treatment of MDR leukemia. |
format | Online Article Text |
id | pubmed-7006299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-70062992020-02-07 The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 Hyun, Jae-Hee Kang, Jung-Il Kim, Sang-Cheol Kim, Elvira Kang, Ji-Hoon Kwon, Jung-Mi Park, Doek-Bae Lee, Young-Jae Yoo, Eun-Sook Kang, Hee-Kyoung Toxicol Res Article The present study investigated the anti-proliferative and chemosensitizing effects of Crinum asiaticum var. japonicum against multi-drug resistant (MDR) cancer cells. The 80% methanol extract, chloroform (CHCI(3)) fraction and butanol (BuOH) fraction of C asiaticum inhibited the growth of mitoxantrone (MX) resistant HL-60 (HL-60/MX2) cells. When HL-60/MX2 cells were treated with the CHCI(3) and BuOH fractions, DNA ladder and sub-G1 hypodiploid cells were observed. Furthermore, the fractions reduced Bcl-2 mRNA levels, whereas Bax mRNA levels were increased. These results suggest that the inhibitory effect of C. asiaticum on the growth of the HL-60/MX2 cells might arise from the induction of apoptosis. Treatment of HL-60/MX2 cells with the fractions markedly decreased the mRNA levels of the multi-drug resistance protein-1 and breast cancer resistance protein. The CHCI3 fraction and hexane fraction increased MX accumulation in HL-60/MX2 cells. These results imply that the CHCI(3) fraction of C asiaticum plays a pivotal role as a chemosensitizer. We suggest that components of C asiaticum might have a therapeutic potential for the treatment of MDR leukemia. Springer Singapore 2008-03-01 2008-03 /pmc/articles/PMC7006299/ /pubmed/32038774 http://dx.doi.org/10.5487/TR.2008.24.1.029 Text en © Korean Society of Toxicology 2008 This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hyun, Jae-Hee Kang, Jung-Il Kim, Sang-Cheol Kim, Elvira Kang, Ji-Hoon Kwon, Jung-Mi Park, Doek-Bae Lee, Young-Jae Yoo, Eun-Sook Kang, Hee-Kyoung The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title | The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title_full | The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title_fullStr | The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title_full_unstemmed | The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title_short | The Effects of Crinum asiaticum on the Apoptosis Induction and the Reversal of Multidrug Resistance in HL-60/MX2 |
title_sort | effects of crinum asiaticum on the apoptosis induction and the reversal of multidrug resistance in hl-60/mx2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006299/ https://www.ncbi.nlm.nih.gov/pubmed/32038774 http://dx.doi.org/10.5487/TR.2008.24.1.029 |
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