SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>

Several methodologies have been proposed in order to establish anticancer action, mainly focused on in vitro cytotoxicity valuation on neoplasic cell lines derived from human cancer. However, most of these cell lines are metabolically incompetent, restricting model sensibility and generating false n...

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Auteurs principaux: Stephanie O. PRIETO, Fabio A. ARISTIZÁBAL G.
Format: article
Langue:EN
Publié: Universidad de Antioquia 2009
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MTT
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spelling oai:doaj.org-article:bca96ac0ab6d40b48a742f43e51f71bb2021-11-19T04:15:44ZSENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>0121-40042145-2660https://doaj.org/article/bca96ac0ab6d40b48a742f43e51f71bb2009-07-01T00:00:00Zhttps://revistas.udea.edu.co/index.php/vitae/article/view/1933https://doaj.org/toc/0121-4004https://doaj.org/toc/2145-2660Several methodologies have been proposed in order to establish anticancer action, mainly focused on in vitro cytotoxicity valuation on neoplasic cell lines derived from human cancer. However, most of these cell lines are metabolically incompetent, restricting model sensibility and generating false negative answers. Hep-G2 cell line is widely used because of its high sensibility reflecting phase I and II activity of some enzymes of phase I and II, which play an important role in activation and detoxification of xenobiotics. In this study, Hep-G2 is used as a model to find cytotoxic activity produced by 2-amino- 1-methyl-6-phenylimidazo [4,5-b]pyridine (PhIP) and Cyclophosphamide, in presence or absence of inductor agents. This analysis was carried out by measuring indirectly viable number of cells with assays like MTT and resazurine staining. In addition, the possibility of co-cultures with other cell lines was evaluated according to strengthen method sensibility. Cytotoxicity of PhIP and cyclophosphamide was observed with the cellular staining methods. For this reason a co-culture system was established. The answer was similar to independent cell lines. These results propose that pre-treated Hep-G2 cells with some inductive agents show sensibility by PhIP as different authors postulate. Stephanie O. PRIETOFabio A. ARISTIZÁBAL G.Universidad de AntioquiaarticlecytochromeHep-G2enzyme inducercytotoxicityMTTresazurina.Food processing and manufactureTP368-456Pharmaceutical industryHD9665-9675ENVitae, Vol 16, Iss 2 (2009)
institution DOAJ
collection DOAJ
language EN
topic cytochrome
Hep-G2
enzyme inducer
cytotoxicity
MTT
resazurina.
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
spellingShingle cytochrome
Hep-G2
enzyme inducer
cytotoxicity
MTT
resazurina.
Food processing and manufacture
TP368-456
Pharmaceutical industry
HD9665-9675
Stephanie O. PRIETO
Fabio A. ARISTIZÁBAL G.
SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
description Several methodologies have been proposed in order to establish anticancer action, mainly focused on in vitro cytotoxicity valuation on neoplasic cell lines derived from human cancer. However, most of these cell lines are metabolically incompetent, restricting model sensibility and generating false negative answers. Hep-G2 cell line is widely used because of its high sensibility reflecting phase I and II activity of some enzymes of phase I and II, which play an important role in activation and detoxification of xenobiotics. In this study, Hep-G2 is used as a model to find cytotoxic activity produced by 2-amino- 1-methyl-6-phenylimidazo [4,5-b]pyridine (PhIP) and Cyclophosphamide, in presence or absence of inductor agents. This analysis was carried out by measuring indirectly viable number of cells with assays like MTT and resazurine staining. In addition, the possibility of co-cultures with other cell lines was evaluated according to strengthen method sensibility. Cytotoxicity of PhIP and cyclophosphamide was observed with the cellular staining methods. For this reason a co-culture system was established. The answer was similar to independent cell lines. These results propose that pre-treated Hep-G2 cells with some inductive agents show sensibility by PhIP as different authors postulate.
format article
author Stephanie O. PRIETO
Fabio A. ARISTIZÁBAL G.
author_facet Stephanie O. PRIETO
Fabio A. ARISTIZÁBAL G.
author_sort Stephanie O. PRIETO
title SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
title_short SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
title_full SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
title_fullStr SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
title_full_unstemmed SENSITIVILITY PROFILE HEP-G2 AS A MODEL OF CYTOTOXIC ACTIVITY DETERMINATION OF BIOACTIVATED XENOBIOTICS VIA CYP <sub>450</sub>
title_sort sensitivility profile hep-g2 as a model of cytotoxic activity determination of bioactivated xenobiotics via cyp <sub>450</sub>
publisher Universidad de Antioquia
publishDate 2009
url https://doaj.org/article/bca96ac0ab6d40b48a742f43e51f71bb
work_keys_str_mv AT stephanieoprieto sensitivilityprofilehepg2asamodelofcytotoxicactivitydeterminationofbioactivatedxenobioticsviacypsub450sub
AT fabioaaristizabalg sensitivilityprofilehepg2asamodelofcytotoxicactivitydeterminationofbioactivatedxenobioticsviacypsub450sub
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