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Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study
The aim of this study was to examine the effect of crude bile on the human HepG2 and CCRF-CEM cell lines. Cells were exposed to different dilutions of bile. Antiproliferative effects were determined by the cytotoxic MTT assay. Cells undergoing apoptosis were identified by terminal deoxynucleotidyl t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shiraz University of Medical Sciences
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565200/ https://www.ncbi.nlm.nih.gov/pubmed/23390333 |
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author | Azarpira, Negar Rastegar, Fatemeh Amiri, Maryam Esfandiari, Elaheh Geramizadeh, Bita |
author_facet | Azarpira, Negar Rastegar, Fatemeh Amiri, Maryam Esfandiari, Elaheh Geramizadeh, Bita |
author_sort | Azarpira, Negar |
collection | PubMed |
description | The aim of this study was to examine the effect of crude bile on the human HepG2 and CCRF-CEM cell lines. Cells were exposed to different dilutions of bile. Antiproliferative effects were determined by the cytotoxic MTT assay. Cells undergoing apoptosis were identified by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. Bile administration resulted in dose-dependent cytotoxicity in both HepG2 and CCRF-CEM cell lines. Incubated cells exhibited morphologic features of apoptosis. Bile has significant cytotoxic activity in HepG2 and CCRF-CEM cancer cells via induction of apoptosis. The mechanism of apoptosis needs to be further evaluated. It may have clinical utility in the treatment of cancer after in vivo confirmation of activity. |
format | Online Article Text |
id | pubmed-3565200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Shiraz University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-35652002013-02-06 Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study Azarpira, Negar Rastegar, Fatemeh Amiri, Maryam Esfandiari, Elaheh Geramizadeh, Bita Iran J Med Sci Brief Report The aim of this study was to examine the effect of crude bile on the human HepG2 and CCRF-CEM cell lines. Cells were exposed to different dilutions of bile. Antiproliferative effects were determined by the cytotoxic MTT assay. Cells undergoing apoptosis were identified by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay. Bile administration resulted in dose-dependent cytotoxicity in both HepG2 and CCRF-CEM cell lines. Incubated cells exhibited morphologic features of apoptosis. Bile has significant cytotoxic activity in HepG2 and CCRF-CEM cancer cells via induction of apoptosis. The mechanism of apoptosis needs to be further evaluated. It may have clinical utility in the treatment of cancer after in vivo confirmation of activity. Shiraz University of Medical Sciences 2012-12 /pmc/articles/PMC3565200/ /pubmed/23390333 Text en © 2011: Iranian Journal of Medical Sciences |
spellingShingle | Brief Report Azarpira, Negar Rastegar, Fatemeh Amiri, Maryam Esfandiari, Elaheh Geramizadeh, Bita Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title | Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title_full | Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title_fullStr | Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title_full_unstemmed | Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title_short | Comparison of Cytotoxic Activity of Bile on HepG2 and CCRF-CEM Cell Lines: An in Vitro Study |
title_sort | comparison of cytotoxic activity of bile on hepg2 and ccrf-cem cell lines: an in vitro study |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565200/ https://www.ncbi.nlm.nih.gov/pubmed/23390333 |
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