Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549

Background and objective The spider venom may inspire new drugs to treat cancer. The aim of this study is to investigate the effects and mechanisms of spider venom on lung adenocarcinoma cell A549. Methods The proliferation of lung adenocarcinoma A549 cells was detected by MTT. The apoptosis rate wa...

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Main Authors: Zengxiang HU, Yulei DU, Quanxi LIU, Yuan WANG
Format: Article
Language:zho
Published: Chinese Anti-Cancer Association; Chinese Antituberculosis Association 2010-10-01
Series:Chinese Journal of Lung Cancer
Subjects:
Online Access:http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.02&path[]=2091
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spelling doaj-d9969c33892442229b016ae17cba18cd2020-11-24T22:43:49ZzhoChinese Anti-Cancer Association; Chinese Antituberculosis AssociationChinese Journal of Lung Cancer1009-34191999-61872010-10-011310933936Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549Zengxiang HUYulei DUQuanxi LIUYuan WANGYuan WANGBackground and objective The spider venom may inspire new drugs to treat cancer. The aim of this study is to investigate the effects and mechanisms of spider venom on lung adenocarcinoma cell A549. Methods The proliferation of lung adenocarcinoma A549 cells was detected by MTT. The apoptosis rate was observed with MTT assay and flow cytometer. The activity of catalase was detected by colorimetry. The malondialdehyde (MDA) content was determined by improved thiobarbituric acid fluorometric method. The expression of P38MAPK protein was analyzed with Western blot. Results Spider venom can remarkably inhibite the proliferation of lung adenocarcinoma A549 cells, increased activity of catalase and MDA content, down-regulated expression of P38MAPK compared with the control group. Conclusion The reduced proliferation of lung adenocarcinoma A549 cells by spider venom is may be associated with the increased of activity of catalase and MDA content and decreased expression of P38MAPK.http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.02&path[]=2091A549 cellsSpider venomP38MAPKAnti-cancer drug
collection DOAJ
language zho
format Article
sources DOAJ
author Zengxiang HU
Yulei DU
Quanxi LIU
Yuan WANG
Yuan WANG
spellingShingle Zengxiang HU
Yulei DU
Quanxi LIU
Yuan WANG
Yuan WANG
Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
Chinese Journal of Lung Cancer
A549 cells
Spider venom
P38MAPK
Anti-cancer drug
author_facet Zengxiang HU
Yulei DU
Quanxi LIU
Yuan WANG
Yuan WANG
author_sort Zengxiang HU
title Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
title_short Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
title_full Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
title_fullStr Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
title_full_unstemmed Effects of the Spider Venom on proliferation of Human Lung Adenocarcinoma Cell A549
title_sort effects of the spider venom on proliferation of human lung adenocarcinoma cell a549
publisher Chinese Anti-Cancer Association; Chinese Antituberculosis Association
series Chinese Journal of Lung Cancer
issn 1009-3419
1999-6187
publishDate 2010-10-01
description Background and objective The spider venom may inspire new drugs to treat cancer. The aim of this study is to investigate the effects and mechanisms of spider venom on lung adenocarcinoma cell A549. Methods The proliferation of lung adenocarcinoma A549 cells was detected by MTT. The apoptosis rate was observed with MTT assay and flow cytometer. The activity of catalase was detected by colorimetry. The malondialdehyde (MDA) content was determined by improved thiobarbituric acid fluorometric method. The expression of P38MAPK protein was analyzed with Western blot. Results Spider venom can remarkably inhibite the proliferation of lung adenocarcinoma A549 cells, increased activity of catalase and MDA content, down-regulated expression of P38MAPK compared with the control group. Conclusion The reduced proliferation of lung adenocarcinoma A549 cells by spider venom is may be associated with the increased of activity of catalase and MDA content and decreased expression of P38MAPK.
topic A549 cells
Spider venom
P38MAPK
Anti-cancer drug
url http://www.lungca.org/index.php?journal=01&page=article&op=viewFile&path[]=10.3779%2Fj.issn.1009-3419.2010.10.02&path[]=2091
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AT quanxiliu effectsofthespidervenomonproliferationofhumanlungadenocarcinomacella549
AT yuanwang effectsofthespidervenomonproliferationofhumanlungadenocarcinomacella549
AT yuanwang effectsofthespidervenomonproliferationofhumanlungadenocarcinomacella549
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