In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer
碩士 === 朝陽科技大學 === 生化科技研究所碩士班 === 98 === Colon carcinoma is one of the most common malignant diseases worldwide. Previous studies reported destruxins B, one of the secondary metabolites of Metarhiziu anisopliae has potent growth suppression effect on human HT-29 adenocarcinoma cells. The purpose of t...
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ndltd-TW-098CYUT51030402015-10-13T18:35:38Z http://ndltd.ncl.edu.tw/handle/11304542819274754242 In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer 黑殭菌素B在動物模式中對人類大腸癌腫瘤的抑制效果之研究探討 Wan-chun Liao 廖婉君 碩士 朝陽科技大學 生化科技研究所碩士班 98 Colon carcinoma is one of the most common malignant diseases worldwide. Previous studies reported destruxins B, one of the secondary metabolites of Metarhiziu anisopliae has potent growth suppression effect on human HT-29 adenocarcinoma cells. The purpose of this study is to compare, in vitro and in vivo, the anti-colon cancer activities of destruxin B and investigate the in vivo anti-colon cancer pathway of destruxin B. The destruxins were isolated and purified according to the previous report (Chen et al., 1999) and characterized by HPLC, ESI-MASS and 1H NMR spectroscopies. A significant inhibition in cell viability was observed upon treatments with various concentrations of destruxin B and was in a dose-dependent manner. The IC50 of destruxin B at 48 hours was 2μM on HT-29. At the end of the experiment, Destruxin B, at low dose concentration ( 0.6 mg/kg/day) could inhibit tumor growth in a xenograft mice model and the caspase-3 is activated after 2 weeks treatment of destruxin B. In conclusion, destruxin B was suggested potentially to be explored as a new therapeutic agent against human colorectal carcinoma cancer. Chi-Chiang Yang Yew-Min Tzeng 楊繼江 曾耀銘 2010 學位論文 ; thesis 64 en_US |
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碩士 === 朝陽科技大學 === 生化科技研究所碩士班 === 98 === Colon carcinoma is one of the most common malignant diseases worldwide. Previous studies reported destruxins B, one of the secondary metabolites of Metarhiziu anisopliae has potent growth suppression effect on human HT-29 adenocarcinoma cells. The purpose of this study is to compare, in vitro and in vivo, the anti-colon cancer activities of destruxin B and investigate the in vivo anti-colon cancer pathway of destruxin B. The destruxins were isolated and purified according to the previous report (Chen et al., 1999) and characterized by HPLC, ESI-MASS and 1H NMR spectroscopies. A significant inhibition in cell viability was observed upon treatments with various concentrations of destruxin B and was in a dose-dependent manner. The IC50 of destruxin B at 48 hours was 2μM on HT-29. At the end of the experiment, Destruxin B, at low dose concentration ( 0.6 mg/kg/day) could inhibit tumor growth in a xenograft mice model and the caspase-3 is activated after 2 weeks treatment of destruxin B. In conclusion, destruxin B was suggested potentially to be explored as a new therapeutic agent against human colorectal carcinoma cancer.
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author2 |
Chi-Chiang Yang |
author_facet |
Chi-Chiang Yang Wan-chun Liao 廖婉君 |
author |
Wan-chun Liao 廖婉君 |
spellingShingle |
Wan-chun Liao 廖婉君 In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
author_sort |
Wan-chun Liao |
title |
In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
title_short |
In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
title_full |
In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
title_fullStr |
In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
title_full_unstemmed |
In Vivo Inhibitory Effects of Destruxin B on Human Colorectal Cancer |
title_sort |
in vivo inhibitory effects of destruxin b on human colorectal cancer |
publishDate |
2010 |
url |
http://ndltd.ncl.edu.tw/handle/11304542819274754242 |
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