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Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells

We previously showed that the B cell leukemia cell line NALM-6 had the highest susceptibility among a number of leukemia cell lines to spiruchostatin B (SP-B), a potent histone deacetylase (HDAC) inhibitor. We also showed that SP-B-induced cytotoxicity depended on induction of apoptosis that was med...

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Autores principales: KANNO, SYU-ICHI, MAEDA, NAOYUKI, TOMIZAWA, AYAKO, YOMOGIDA, SHIN, KATOH, TADASHI, ISHIKAWA, MASAAKI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582725/
https://www.ncbi.nlm.nih.gov/pubmed/22684370
http://dx.doi.org/10.3892/ijo.2012.1507
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author KANNO, SYU-ICHI
MAEDA, NAOYUKI
TOMIZAWA, AYAKO
YOMOGIDA, SHIN
KATOH, TADASHI
ISHIKAWA, MASAAKI
author_facet KANNO, SYU-ICHI
MAEDA, NAOYUKI
TOMIZAWA, AYAKO
YOMOGIDA, SHIN
KATOH, TADASHI
ISHIKAWA, MASAAKI
author_sort KANNO, SYU-ICHI
collection PubMed
description We previously showed that the B cell leukemia cell line NALM-6 had the highest susceptibility among a number of leukemia cell lines to spiruchostatin B (SP-B), a potent histone deacetylase (HDAC) inhibitor. We also showed that SP-B-induced cytotoxicity depended on induction of apoptosis that was mediated by p21(waf1/cip1) expression. In the present study, we generated and characterized a stable, SP-B-resistant NALM-6 cell line (NALM-6/SP-B) by continuous exposure to SP-B, starting with a low SP-B concentration. NALM-6/SP-B cells were also more resistant to FK228, which has a similar chemical structure to SP-B, and were slightly more resistant to the P-gp substrates doxorubicin and vincristine than parental cells, but displayed similar susceptibility to other HDAC inhibitors and to paclitaxel as the parental cells. There was little change in the basal mRNA expression of HDAC1, p53, Bax, Bcl-2, Fas, caspase-3, c-Myc and MDR1 in NALM-6/SP-B compared to parental cells, but the mRNA expression of p21(waf1/cip1) was decreased. The introduction of an exogenous p21(waf1/cip1) expression vector restored SP-B induction of NALM-6/SP-B cell apoptosis. Moreover, overexpressed p21(waf1/cip1) enhanced SP-B induction of the apoptosis of the human erythroleukemia leukemia cell line K562 which is less susceptible to SP-B than NALM-6 cells. These results suggest that downregulation of p21(waf1/cip1), which is a characteristic feature of NALM-6/SP-B cells, was important for their resistance to SP-B, and that this SP-B resistance could be overcome by the introduction of exogenous p21(waf1/cip1). Furthermore, introduction of p21(waf1/cip1) to other leukemia cells such as K562 may enhance their susceptibility to SP-B. This is the first report of the characterization of SP-B-resistant cells and of the effect of overexpressed p21(waf1/cip1) on the resistance or susceptibility of human leukemia cells to SP-B.
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spelling pubmed-35827252013-03-04 Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells KANNO, SYU-ICHI MAEDA, NAOYUKI TOMIZAWA, AYAKO YOMOGIDA, SHIN KATOH, TADASHI ISHIKAWA, MASAAKI Int J Oncol Articles We previously showed that the B cell leukemia cell line NALM-6 had the highest susceptibility among a number of leukemia cell lines to spiruchostatin B (SP-B), a potent histone deacetylase (HDAC) inhibitor. We also showed that SP-B-induced cytotoxicity depended on induction of apoptosis that was mediated by p21(waf1/cip1) expression. In the present study, we generated and characterized a stable, SP-B-resistant NALM-6 cell line (NALM-6/SP-B) by continuous exposure to SP-B, starting with a low SP-B concentration. NALM-6/SP-B cells were also more resistant to FK228, which has a similar chemical structure to SP-B, and were slightly more resistant to the P-gp substrates doxorubicin and vincristine than parental cells, but displayed similar susceptibility to other HDAC inhibitors and to paclitaxel as the parental cells. There was little change in the basal mRNA expression of HDAC1, p53, Bax, Bcl-2, Fas, caspase-3, c-Myc and MDR1 in NALM-6/SP-B compared to parental cells, but the mRNA expression of p21(waf1/cip1) was decreased. The introduction of an exogenous p21(waf1/cip1) expression vector restored SP-B induction of NALM-6/SP-B cell apoptosis. Moreover, overexpressed p21(waf1/cip1) enhanced SP-B induction of the apoptosis of the human erythroleukemia leukemia cell line K562 which is less susceptible to SP-B than NALM-6 cells. These results suggest that downregulation of p21(waf1/cip1), which is a characteristic feature of NALM-6/SP-B cells, was important for their resistance to SP-B, and that this SP-B resistance could be overcome by the introduction of exogenous p21(waf1/cip1). Furthermore, introduction of p21(waf1/cip1) to other leukemia cells such as K562 may enhance their susceptibility to SP-B. This is the first report of the characterization of SP-B-resistant cells and of the effect of overexpressed p21(waf1/cip1) on the resistance or susceptibility of human leukemia cells to SP-B. D.A. Spandidos 2012-06-06 /pmc/articles/PMC3582725/ /pubmed/22684370 http://dx.doi.org/10.3892/ijo.2012.1507 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
KANNO, SYU-ICHI
MAEDA, NAOYUKI
TOMIZAWA, AYAKO
YOMOGIDA, SHIN
KATOH, TADASHI
ISHIKAWA, MASAAKI
Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title_full Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title_fullStr Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title_full_unstemmed Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title_short Characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin B (SP-B) and effect of overexpressed p21(waf1/cip1) on the SP-B resistance or susceptibility of human leukemia cells
title_sort characterization of cells resistant to the potent histone deacetylase inhibitor spiruchostatin b (sp-b) and effect of overexpressed p21(waf1/cip1) on the sp-b resistance or susceptibility of human leukemia cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582725/
https://www.ncbi.nlm.nih.gov/pubmed/22684370
http://dx.doi.org/10.3892/ijo.2012.1507
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