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Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells
BACKGROUND: Houttuynia cordata Thunb (HCT) is commonly used in Taiwan and other Asian countries as an anti-inflammatory, antibacterial and antiviral herbal medicine. In this study, we investigated the anti-human lung cancer activity and growth inhibition mechanisms of HCT in human lung cancer A549 c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610241/ https://www.ncbi.nlm.nih.gov/pubmed/23506616 http://dx.doi.org/10.1186/1423-0127-20-18 |
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author | Chen, Yuh-Fung Yang, Jai-Sing Chang, Wen-Shin Tsai, Shih-Chang Peng, Shu-Fen Zhou, Yuan-Ru |
author_facet | Chen, Yuh-Fung Yang, Jai-Sing Chang, Wen-Shin Tsai, Shih-Chang Peng, Shu-Fen Zhou, Yuan-Ru |
author_sort | Chen, Yuh-Fung |
collection | PubMed |
description | BACKGROUND: Houttuynia cordata Thunb (HCT) is commonly used in Taiwan and other Asian countries as an anti-inflammatory, antibacterial and antiviral herbal medicine. In this study, we investigated the anti-human lung cancer activity and growth inhibition mechanisms of HCT in human lung cancer A549 cells. RESULTS: In order to investigate effects of HCT on A549 cells, MTT assay was used to evaluate cell viability. Flow cytometry was employed for cell cycle analysis, DAPI staining, and the Comet assay was used for DNA fragmentation and DNA condensation. Western blot analysis was used to analyze cell cycle and apoptotic related protein levels. HCT induced morphological changes including cell shrinkage and rounding. HCT increased the G(0)/G(1) and Sub-G(1) cell (apoptosis) populations and HCT increased DNA fragmentation and DNA condensation as revealed by DAPI staining and the Comet assay. HCT induced activation of caspase-8 and caspase-3. Fas/CD95 protein levels were increased in HCT-treated A549 cells. The G(0)/G(1) phase and apoptotic related protein levels of cyclin D1, cyclin A, CDK 4 and CDK 2 were decreased, and p27, caspase-8 and caspase-3 were increased in A549 cells after HCT treatment. CONCLUSIONS: The results demonstrated that HCT-induced G(0)/G(1) phase arrest and Fas/CD95-dependent apoptotic cell death in A549 cells |
format | Online Article Text |
id | pubmed-3610241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36102412013-03-29 Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells Chen, Yuh-Fung Yang, Jai-Sing Chang, Wen-Shin Tsai, Shih-Chang Peng, Shu-Fen Zhou, Yuan-Ru J Biomed Sci Research BACKGROUND: Houttuynia cordata Thunb (HCT) is commonly used in Taiwan and other Asian countries as an anti-inflammatory, antibacterial and antiviral herbal medicine. In this study, we investigated the anti-human lung cancer activity and growth inhibition mechanisms of HCT in human lung cancer A549 cells. RESULTS: In order to investigate effects of HCT on A549 cells, MTT assay was used to evaluate cell viability. Flow cytometry was employed for cell cycle analysis, DAPI staining, and the Comet assay was used for DNA fragmentation and DNA condensation. Western blot analysis was used to analyze cell cycle and apoptotic related protein levels. HCT induced morphological changes including cell shrinkage and rounding. HCT increased the G(0)/G(1) and Sub-G(1) cell (apoptosis) populations and HCT increased DNA fragmentation and DNA condensation as revealed by DAPI staining and the Comet assay. HCT induced activation of caspase-8 and caspase-3. Fas/CD95 protein levels were increased in HCT-treated A549 cells. The G(0)/G(1) phase and apoptotic related protein levels of cyclin D1, cyclin A, CDK 4 and CDK 2 were decreased, and p27, caspase-8 and caspase-3 were increased in A549 cells after HCT treatment. CONCLUSIONS: The results demonstrated that HCT-induced G(0)/G(1) phase arrest and Fas/CD95-dependent apoptotic cell death in A549 cells BioMed Central 2013-03-19 /pmc/articles/PMC3610241/ /pubmed/23506616 http://dx.doi.org/10.1186/1423-0127-20-18 Text en Copyright ©2013 Chen 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 Chen, Yuh-Fung Yang, Jai-Sing Chang, Wen-Shin Tsai, Shih-Chang Peng, Shu-Fen Zhou, Yuan-Ru Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title | Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title_full | Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title_fullStr | Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title_full_unstemmed | Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title_short | Houttuynia cordata Thunb extract modulates G(0)/G(1) arrest and Fas/CD95-mediated death receptor apoptotic cell death in human lung cancer A549 cells |
title_sort | houttuynia cordata thunb extract modulates g(0)/g(1) arrest and fas/cd95-mediated death receptor apoptotic cell death in human lung cancer a549 cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610241/ https://www.ncbi.nlm.nih.gov/pubmed/23506616 http://dx.doi.org/10.1186/1423-0127-20-18 |
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