Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line

Onion (Allium cepa) is being studied as a potential anticancer agent, but little is known regarding its effect in multidrug resistance (MDR) cells. In this work, the cytotoxicity of crude onion extract (OE) and fractioned extract (aqueous, methanolic and ethyl acetate), as well as some onion compounds (quercetin and propyl disulfide) were evaluated in Lucena MDR human erythroleukemic and its K562 parental cell line. The capacity of OE to induce apoptosis and/or necrosis in these cells, the possible participation of oxidative stress and DNA damage were also assessed. Similar sensitivities were obtained for both tumoral cells, however only OE caused significant effects in the cells. In K562 cells, a significant increase of apoptosis was verified while the Lucena cells experienced a significant increase of necrosis. An antioxidant capacity was verified for OE discarding oxidative damage. However, OE provoked similar significant DNA damage in both cell lines. Thus, the OE capacity to overcome the MDR phenotype suggests anti-MDR action of OE.

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Main Authors: Votto,Ana P. S, Domingues,Beatriz S, de Souza,Michele M, da Silva Júnior,Flavio M. R, Caldas,Sergiane S, Filgueira,Daza M. V. B, Clementin,Rosilene M, Primel,Ednei G, Vallochi,Adriana L, Furlong,Eliana B, Trindade,Gilma S
Format: Digital revista
Language:English
Published: Sociedad de Biología de Chile 2010
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602010000400007
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spelling oai:scielo:S0716-976020100004000072011-02-01Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell lineVotto,Ana P. SDomingues,Beatriz Sde Souza,Michele Mda Silva Júnior,Flavio M. RCaldas,Sergiane SFilgueira,Daza M. V. BClementin,Rosilene MPrimel,Ednei GVallochi,Adriana LFurlong,Eliana BTrindade,Gilma S antioxidant apoptosis and/or necrosis DNA damage MDR phenotype onion (Allium cepa) tumoral cell Onion (Allium cepa) is being studied as a potential anticancer agent, but little is known regarding its effect in multidrug resistance (MDR) cells. In this work, the cytotoxicity of crude onion extract (OE) and fractioned extract (aqueous, methanolic and ethyl acetate), as well as some onion compounds (quercetin and propyl disulfide) were evaluated in Lucena MDR human erythroleukemic and its K562 parental cell line. The capacity of OE to induce apoptosis and/or necrosis in these cells, the possible participation of oxidative stress and DNA damage were also assessed. Similar sensitivities were obtained for both tumoral cells, however only OE caused significant effects in the cells. In K562 cells, a significant increase of apoptosis was verified while the Lucena cells experienced a significant increase of necrosis. An antioxidant capacity was verified for OE discarding oxidative damage. However, OE provoked similar significant DNA damage in both cell lines. Thus, the OE capacity to overcome the MDR phenotype suggests anti-MDR action of OE.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.43 n.4 20102010-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602010000400007en10.4067/S0716-97602010000400007
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country Chile
countrycode CL
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region America del Sur
libraryname SciELO
language English
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author Votto,Ana P. S
Domingues,Beatriz S
de Souza,Michele M
da Silva Júnior,Flavio M. R
Caldas,Sergiane S
Filgueira,Daza M. V. B
Clementin,Rosilene M
Primel,Ednei G
Vallochi,Adriana L
Furlong,Eliana B
Trindade,Gilma S
spellingShingle Votto,Ana P. S
Domingues,Beatriz S
de Souza,Michele M
da Silva Júnior,Flavio M. R
Caldas,Sergiane S
Filgueira,Daza M. V. B
Clementin,Rosilene M
Primel,Ednei G
Vallochi,Adriana L
Furlong,Eliana B
Trindade,Gilma S
Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
author_facet Votto,Ana P. S
Domingues,Beatriz S
de Souza,Michele M
da Silva Júnior,Flavio M. R
Caldas,Sergiane S
Filgueira,Daza M. V. B
Clementin,Rosilene M
Primel,Ednei G
Vallochi,Adriana L
Furlong,Eliana B
Trindade,Gilma S
author_sort Votto,Ana P. S
title Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
title_short Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
title_full Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
title_fullStr Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
title_full_unstemmed Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
title_sort toxicity mechanisms of onion (allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line
description Onion (Allium cepa) is being studied as a potential anticancer agent, but little is known regarding its effect in multidrug resistance (MDR) cells. In this work, the cytotoxicity of crude onion extract (OE) and fractioned extract (aqueous, methanolic and ethyl acetate), as well as some onion compounds (quercetin and propyl disulfide) were evaluated in Lucena MDR human erythroleukemic and its K562 parental cell line. The capacity of OE to induce apoptosis and/or necrosis in these cells, the possible participation of oxidative stress and DNA damage were also assessed. Similar sensitivities were obtained for both tumoral cells, however only OE caused significant effects in the cells. In K562 cells, a significant increase of apoptosis was verified while the Lucena cells experienced a significant increase of necrosis. An antioxidant capacity was verified for OE discarding oxidative damage. However, OE provoked similar significant DNA damage in both cell lines. Thus, the OE capacity to overcome the MDR phenotype suggests anti-MDR action of OE.
publisher Sociedad de Biología de Chile
publishDate 2010
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602010000400007
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