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Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line
BACKGROUND: Six plants from Thailand were evaluated for their cytotoxicity and apoptosis induction in human hepatocarcinoma (HepG2) as compared to normal African green monkey kidney epithelial cell lines. METHODS: Ethanol-water crude extracts of the six plants were tested with neutral red assay for...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224580/ https://www.ncbi.nlm.nih.gov/pubmed/22041055 http://dx.doi.org/10.1186/1749-8546-6-39 |
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author | Machana, Sasipawan Weerapreeyakul, Natthida Barusrux, Sahapat Nonpunya, Apiyada Sripanidkulchai, Bungorn Thitimetharoch, Thaweesak |
author_facet | Machana, Sasipawan Weerapreeyakul, Natthida Barusrux, Sahapat Nonpunya, Apiyada Sripanidkulchai, Bungorn Thitimetharoch, Thaweesak |
author_sort | Machana, Sasipawan |
collection | PubMed |
description | BACKGROUND: Six plants from Thailand were evaluated for their cytotoxicity and apoptosis induction in human hepatocarcinoma (HepG2) as compared to normal African green monkey kidney epithelial cell lines. METHODS: Ethanol-water crude extracts of the six plants were tested with neutral red assay for their cytotoxicity after 24 hours of exposure to the cells. Apoptotic induction was tested in the HepG2 cells with diamidino-2-phenylindole staining. DNA fragmentation, indicative of apoptosis, was analyzed with agarose gel electrophoresis. Alkylation, indicative of DNA damage, was also evaluated in vitro by 4-(4'-nitrobenzyl) pyridine assay. RESULTS: The extract of Pinus kesiya showed the highest selectivity (selectivity index = 9.6) and potent cytotoxicity in the HepG2 cell line, with an IC(50 )value of 52.0 ± 5.8 μg/ml (mean ± standard deviation). Extract of Catimbium speciosum exerted cytotoxicity with an IC(50 )value of 55.7 ± 8.1 μg/ml. Crude extracts from Glochidion daltonii, Cladogynos orientalis, Acorus tatarinowii and Amomum villosum exhibited cytotoxicity with IC(50 )values ranging 100-500 μg/ml. All crude extracts showed different alkylating abilities in vitro. Extracts of P. kesiya, C. speciosum and C. orientalis caused nuclei morphological changes and DNA laddering. CONCLUSION: The extracts of C. speciosum, C. orientalis and P. kesiya induced apoptosis. Among the three plants, P. kesiya possessed the most robust anticancer activity, with specific selectivity against HepG2 cells. |
format | Online Article Text |
id | pubmed-3224580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32245802011-11-30 Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line Machana, Sasipawan Weerapreeyakul, Natthida Barusrux, Sahapat Nonpunya, Apiyada Sripanidkulchai, Bungorn Thitimetharoch, Thaweesak Chin Med Research BACKGROUND: Six plants from Thailand were evaluated for their cytotoxicity and apoptosis induction in human hepatocarcinoma (HepG2) as compared to normal African green monkey kidney epithelial cell lines. METHODS: Ethanol-water crude extracts of the six plants were tested with neutral red assay for their cytotoxicity after 24 hours of exposure to the cells. Apoptotic induction was tested in the HepG2 cells with diamidino-2-phenylindole staining. DNA fragmentation, indicative of apoptosis, was analyzed with agarose gel electrophoresis. Alkylation, indicative of DNA damage, was also evaluated in vitro by 4-(4'-nitrobenzyl) pyridine assay. RESULTS: The extract of Pinus kesiya showed the highest selectivity (selectivity index = 9.6) and potent cytotoxicity in the HepG2 cell line, with an IC(50 )value of 52.0 ± 5.8 μg/ml (mean ± standard deviation). Extract of Catimbium speciosum exerted cytotoxicity with an IC(50 )value of 55.7 ± 8.1 μg/ml. Crude extracts from Glochidion daltonii, Cladogynos orientalis, Acorus tatarinowii and Amomum villosum exhibited cytotoxicity with IC(50 )values ranging 100-500 μg/ml. All crude extracts showed different alkylating abilities in vitro. Extracts of P. kesiya, C. speciosum and C. orientalis caused nuclei morphological changes and DNA laddering. CONCLUSION: The extracts of C. speciosum, C. orientalis and P. kesiya induced apoptosis. Among the three plants, P. kesiya possessed the most robust anticancer activity, with specific selectivity against HepG2 cells. BioMed Central 2011-10-31 /pmc/articles/PMC3224580/ /pubmed/22041055 http://dx.doi.org/10.1186/1749-8546-6-39 Text en Copyright ©2011 Machana et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Machana, Sasipawan Weerapreeyakul, Natthida Barusrux, Sahapat Nonpunya, Apiyada Sripanidkulchai, Bungorn Thitimetharoch, Thaweesak Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title | Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title_full | Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title_fullStr | Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title_full_unstemmed | Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title_short | Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (HepG2) cell line |
title_sort | cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma (hepg2) cell line |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224580/ https://www.ncbi.nlm.nih.gov/pubmed/22041055 http://dx.doi.org/10.1186/1749-8546-6-39 |
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