<it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line

<p>Abstract</p> <p>Background</p> <p>In the search for anticancer agents, a promising 17-β-estradiol metabolite, 2-methoxyestradiol (2ME2) was found that exerts antiproliferative <it>in vitro </it>and <it>in vivo </it>activity. Since 2ME2 has lim...

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Main Authors: Visagie Michelle H, Joubert Anna M
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Cancer Cell International
Subjects:
Online Access:http://www.cancerci.com/content/11/1/43
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author Visagie Michelle H
Joubert Anna M
author_facet Visagie Michelle H
Joubert Anna M
author_sort Visagie Michelle H
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>In the search for anticancer agents, a promising 17-β-estradiol metabolite, 2-methoxyestradiol (2ME2) was found that exerts antiproliferative <it>in vitro </it>and <it>in vivo </it>activity. Since 2ME2 has limited biological accessibility and rapid metabolic degradation, the purpose of this study was to investigate the <it>in vitro </it>influence exerted by an analogue of 2ME2 namely 2-methoxyestradiol-bis-sulphamate (2MEBM) in a breast adenocarcinoma cell line (MCF-7).</p> <p>Methods</p> <p>This was conducted by investigating 2MEBM's <it>in vitro </it>influence on cell cycle progression, mitochondrial membrane potential and possible production of reactive oxygen species (ROS) generation. <it>In vitro </it>effects of 2MEBM on cell cycle progression was demonstrated by means of flow cytometry using propidium iodide. Hydrogen peroxide and superoxide production was investigated using 2,7-dichlorofluorescein diacetate and hydroethidine, respectively. The probable reduction in the mitochondrial membrane potential was demonstrated using a MitoCapture™ kit.</p> <p>Results</p> <p>Cell cycle progression revealed the presence of a sub-G<sub>1 </sub>apoptotic peak. Reduction of mitochondrial membrane potential after exposure to 2MEBM was demonstrated and an increase in ROS production was also observed.</p> <p>Conclusion</p> <p>This study verified that 2MEBM exposure resulted in apoptosis induction, increased ROS production and reduced mitochondrial membrane potential in a tumorigenic breast epithelial cell line. Data obtained from this project contributes to the unravelling of the <it>in vitro </it>signal transduction of 2MEBM in tumorigenic cell lines.</p>
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spelling doaj.art-d99160b2171a405f9976e6783f56f3132022-12-22T02:50:23ZengBMCCancer Cell International1475-28672011-12-011114310.1186/1475-2867-11-43<it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell lineVisagie Michelle HJoubert Anna M<p>Abstract</p> <p>Background</p> <p>In the search for anticancer agents, a promising 17-β-estradiol metabolite, 2-methoxyestradiol (2ME2) was found that exerts antiproliferative <it>in vitro </it>and <it>in vivo </it>activity. Since 2ME2 has limited biological accessibility and rapid metabolic degradation, the purpose of this study was to investigate the <it>in vitro </it>influence exerted by an analogue of 2ME2 namely 2-methoxyestradiol-bis-sulphamate (2MEBM) in a breast adenocarcinoma cell line (MCF-7).</p> <p>Methods</p> <p>This was conducted by investigating 2MEBM's <it>in vitro </it>influence on cell cycle progression, mitochondrial membrane potential and possible production of reactive oxygen species (ROS) generation. <it>In vitro </it>effects of 2MEBM on cell cycle progression was demonstrated by means of flow cytometry using propidium iodide. Hydrogen peroxide and superoxide production was investigated using 2,7-dichlorofluorescein diacetate and hydroethidine, respectively. The probable reduction in the mitochondrial membrane potential was demonstrated using a MitoCapture™ kit.</p> <p>Results</p> <p>Cell cycle progression revealed the presence of a sub-G<sub>1 </sub>apoptotic peak. Reduction of mitochondrial membrane potential after exposure to 2MEBM was demonstrated and an increase in ROS production was also observed.</p> <p>Conclusion</p> <p>This study verified that 2MEBM exposure resulted in apoptosis induction, increased ROS production and reduced mitochondrial membrane potential in a tumorigenic breast epithelial cell line. Data obtained from this project contributes to the unravelling of the <it>in vitro </it>signal transduction of 2MEBM in tumorigenic cell lines.</p>http://www.cancerci.com/content/11/1/432-methoxyestradiol-bis-sulphamatecell cycle progressionreactive oxygen speciesmitochondrial integrityapoptosisautophagy
spellingShingle Visagie Michelle H
Joubert Anna M
<it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
Cancer Cell International
2-methoxyestradiol-bis-sulphamate
cell cycle progression
reactive oxygen species
mitochondrial integrity
apoptosis
autophagy
title <it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
title_full <it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
title_fullStr <it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
title_full_unstemmed <it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
title_short <it>In vitro </it>effects of 2-methoxyestradiol-bis-sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
title_sort it in vitro it effects of 2 methoxyestradiol bis sulphamate on reactive oxygen species and possible apoptosis induction in a breast adenocarcinoma cell line
topic 2-methoxyestradiol-bis-sulphamate
cell cycle progression
reactive oxygen species
mitochondrial integrity
apoptosis
autophagy
url http://www.cancerci.com/content/11/1/43
work_keys_str_mv AT visagiemichelleh itinvitroiteffectsof2methoxyestradiolbissulphamateonreactiveoxygenspeciesandpossibleapoptosisinductioninabreastadenocarcinomacellline
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