Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells

<p>Abstract</p> <p>Background</p> <p>Dihydroartemisinin (DHA), a semi-synthetic derivative of artemisinin, isolated from the traditional Chinese herb Artemisia annua, is recommended as the first-line anti-malarial drug with low toxicity. DHA has been shown to possess pr...

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Main Authors: Sun Lei, Pan Wen-Liang, Qu Jun-Le, Chen Tong-Sheng, Lu Ying-Ying, Wei Xun-Bin
Format: Article
Language:English
Published: BMC 2009-02-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/16/1/16
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author Sun Lei
Pan Wen-Liang
Qu Jun-Le
Chen Tong-Sheng
Lu Ying-Ying
Wei Xun-Bin
author_facet Sun Lei
Pan Wen-Liang
Qu Jun-Le
Chen Tong-Sheng
Lu Ying-Ying
Wei Xun-Bin
author_sort Sun Lei
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Dihydroartemisinin (DHA), a semi-synthetic derivative of artemisinin, isolated from the traditional Chinese herb Artemisia annua, is recommended as the first-line anti-malarial drug with low toxicity. DHA has been shown to possess promising anticancer activities and induce cancer cell death through apoptotic pathways, although the molecular mechanisms are not well understood.</p> <p>Methods</p> <p>In this study, cell counting kit (CCK-8) assay was employed to evaluate the survival of DHA-treated ASTC-a-1 cells. The induction of apoptosis was detected by Hoechst 33258 and PI staining as well as flow cytometry analysis. Collapse of mitochondrial transmembrane potential (ΔΨ<sub>m</sub>) was measured by dynamic detection under a laser scanning confocal microscope and flow cytometry analysis using Rhodamine123. Caspase-3 activities measured with or without Z-VAD-fmk (a broad spectrum caspase inhibitor) pretreatment by FRET techniques, caspase-3 activity measurement, and western blotting analysis.</p> <p>Results</p> <p>Our results indicated that DHA induced apoptotic cell death in a dose- and time-dependent manner, which was accompanied by mitochondrial morphology changes, the loss of ΔΨ<sub>m </sub>and the activation of caspase-3.</p> <p>Conclusion</p> <p>These results show for the first time that DHA can inhibit proliferation and induce apoptosis via caspase-3-dependent mitochondrial death pathway in ASTC-a-1 cells. Our work may provide evidence for further studies of DHA as a possible anticancer drug in the clinical treatment of lung adenocarcinoma.</p>
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spelling doaj.art-930891baa5004d12ae497ce928bb22242022-12-21T19:11:11ZengBMCJournal of Biomedical Science1021-77701423-01272009-02-011611610.1186/1423-0127-16-16Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cellsSun LeiPan Wen-LiangQu Jun-LeChen Tong-ShengLu Ying-YingWei Xun-Bin<p>Abstract</p> <p>Background</p> <p>Dihydroartemisinin (DHA), a semi-synthetic derivative of artemisinin, isolated from the traditional Chinese herb Artemisia annua, is recommended as the first-line anti-malarial drug with low toxicity. DHA has been shown to possess promising anticancer activities and induce cancer cell death through apoptotic pathways, although the molecular mechanisms are not well understood.</p> <p>Methods</p> <p>In this study, cell counting kit (CCK-8) assay was employed to evaluate the survival of DHA-treated ASTC-a-1 cells. The induction of apoptosis was detected by Hoechst 33258 and PI staining as well as flow cytometry analysis. Collapse of mitochondrial transmembrane potential (ΔΨ<sub>m</sub>) was measured by dynamic detection under a laser scanning confocal microscope and flow cytometry analysis using Rhodamine123. Caspase-3 activities measured with or without Z-VAD-fmk (a broad spectrum caspase inhibitor) pretreatment by FRET techniques, caspase-3 activity measurement, and western blotting analysis.</p> <p>Results</p> <p>Our results indicated that DHA induced apoptotic cell death in a dose- and time-dependent manner, which was accompanied by mitochondrial morphology changes, the loss of ΔΨ<sub>m </sub>and the activation of caspase-3.</p> <p>Conclusion</p> <p>These results show for the first time that DHA can inhibit proliferation and induce apoptosis via caspase-3-dependent mitochondrial death pathway in ASTC-a-1 cells. Our work may provide evidence for further studies of DHA as a possible anticancer drug in the clinical treatment of lung adenocarcinoma.</p>http://www.jbiomedsci.com/content/16/1/16
spellingShingle Sun Lei
Pan Wen-Liang
Qu Jun-Le
Chen Tong-Sheng
Lu Ying-Ying
Wei Xun-Bin
Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
Journal of Biomedical Science
title Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
title_full Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
title_fullStr Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
title_full_unstemmed Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
title_short Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells
title_sort dihydroartemisinin dha induces caspase 3 dependent apoptosis in human lung adenocarcinoma astc a 1 cells
url http://www.jbiomedsci.com/content/16/1/16
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