Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line

Epidemiological and in vitro studies have showed that boron may have anti-carcinogenic properties. Chromosome aberrations assay and sister chromatid exchange assays have showed that boron has no genotoxic effects on cytogenetically stable cell lines. Aim of this investigation is determine to effec...

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Main Authors: Erkan Kahraman, Ismet Deliloglu Gurhan, Mehmet Korkmaz
Format: Article
Language:English
Published: Society of TURAZ AKADEMI 2013-03-01
Series:Medicine Science
Subjects:
Online Access:http://www.ejmanager.com/fulltextpdf.php?mno=27318
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spelling doaj-8539f739d813462a9aff94b7aee963f62020-11-25T00:16:51ZengSociety of TURAZ AKADEMI Medicine Science2147-06342013-03-01214546810.5455/medscience.2012.01.804627318Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell LineErkan Kahraman0Ismet Deliloglu Gurhan1Mehmet Korkmaz2Manisa Cocuk Bakim ve Dogumevi Ege University Department Of Bioengineering Celal Bayar University Faculty of Medicine Department of Medical BiologyEpidemiological and in vitro studies have showed that boron may have anti-carcinogenic properties. Chromosome aberrations assay and sister chromatid exchange assays have showed that boron has no genotoxic effects on cytogenetically stable cell lines. Aim of this investigation is determine to effects of different boron compounds which are boric acid (BA), borax pentahydrate (BP) and disodium pentaborate decahydrate (DPD) ) on exist cytogenetic disruption with variable doses (250, 500 and 1000µM ) on cytogenitically unstabel CCL 62 (HeLa Contaminant) cell line. In order to test this hypothesis, following the boron treatment on the cell lines for cytotoxcity was performed using MTT that cell viability assay. For genotoxicity was used chromosome aberrations assay (CAs) and micronucleus assay (MN), CAs and MN frequency calculated in each boron dose. Boron compaunds effected proliferation of CCL 62 (human amniotic ephitelial) cell lines in a time, species and dose dependent manner. According to data obtained from CAs and MN assays, no significant difference was found between control groups which were not treated any of boron compaund with boron treated groups (p>0,05). In conclusion, we established that BA, BP, and DPD effected proliferation of CCL 62 cell lines in a time, compaund and dose dependent manner, however no evidence was observed suggesting these compounds cause an increase or decrease in the level of existing cytogenetic defects in these cell lines. [Med-Science 2013; 2(1.000): 454-68]http://www.ejmanager.com/fulltextpdf.php?mno=27318BoronBoric acidBorax pentahydrateDisodium pentaborate decahydrateCytotoxicityGenotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Erkan Kahraman
Ismet Deliloglu Gurhan
Mehmet Korkmaz
spellingShingle Erkan Kahraman
Ismet Deliloglu Gurhan
Mehmet Korkmaz
Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
Medicine Science
Boron
Boric acid
Borax pentahydrate
Disodium pentaborate decahydrate
Cytotoxicity
Genotoxicity
author_facet Erkan Kahraman
Ismet Deliloglu Gurhan
Mehmet Korkmaz
author_sort Erkan Kahraman
title Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
title_short Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
title_full Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
title_fullStr Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
title_full_unstemmed Investigation of Possible Genotoxic and Cytotoxic Effects of Differential Boron Compounds in CCL 62 (Hela Contaminant) Human Amniotic Ephitelial Cell Line
title_sort investigation of possible genotoxic and cytotoxic effects of differential boron compounds in ccl 62 (hela contaminant) human amniotic ephitelial cell line
publisher Society of TURAZ AKADEMI
series Medicine Science
issn 2147-0634
publishDate 2013-03-01
description Epidemiological and in vitro studies have showed that boron may have anti-carcinogenic properties. Chromosome aberrations assay and sister chromatid exchange assays have showed that boron has no genotoxic effects on cytogenetically stable cell lines. Aim of this investigation is determine to effects of different boron compounds which are boric acid (BA), borax pentahydrate (BP) and disodium pentaborate decahydrate (DPD) ) on exist cytogenetic disruption with variable doses (250, 500 and 1000µM ) on cytogenitically unstabel CCL 62 (HeLa Contaminant) cell line. In order to test this hypothesis, following the boron treatment on the cell lines for cytotoxcity was performed using MTT that cell viability assay. For genotoxicity was used chromosome aberrations assay (CAs) and micronucleus assay (MN), CAs and MN frequency calculated in each boron dose. Boron compaunds effected proliferation of CCL 62 (human amniotic ephitelial) cell lines in a time, species and dose dependent manner. According to data obtained from CAs and MN assays, no significant difference was found between control groups which were not treated any of boron compaund with boron treated groups (p>0,05). In conclusion, we established that BA, BP, and DPD effected proliferation of CCL 62 cell lines in a time, compaund and dose dependent manner, however no evidence was observed suggesting these compounds cause an increase or decrease in the level of existing cytogenetic defects in these cell lines. [Med-Science 2013; 2(1.000): 454-68]
topic Boron
Boric acid
Borax pentahydrate
Disodium pentaborate decahydrate
Cytotoxicity
Genotoxicity
url http://www.ejmanager.com/fulltextpdf.php?mno=27318
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