Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells
碩士 === 中山醫學大學 === 生化暨生物科技研究所 === 101 === AMP-activated protein kinase (AMPK) is a key player in maintaining energy homeostasis in response to metabolic stress. Published studies indicate that AMPK activation strongly suppresses cell proliferation in non-malignant cells as well as in tumour cells. Th...
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ndltd-TW-101CSMU51070172015-10-13T22:57:21Z http://ndltd.ncl.edu.tw/handle/12191198435622856051 Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells Energi-702對人類惡性骨肉瘤細胞的抗癌機轉研究 Kim Chuan Chan 陳金釧 碩士 中山醫學大學 生化暨生物科技研究所 101 AMP-activated protein kinase (AMPK) is a key player in maintaining energy homeostasis in response to metabolic stress. Published studies indicate that AMPK activation strongly suppresses cell proliferation in non-malignant cells as well as in tumour cells. This study examined the anti-tumor mechanism of Energi-702 (AMPK activator) on osteosarcoma cell lines (U2OS & 143B). Cell viability was detected by the MTT assay and cell morphology was observed after drug administration. After treated with Energi-702 for 24 hour, osteosarcoma cell lysates were collected. Western blot results demonstrate that cell cycle-associate proteins cyclin D1, cyclin E, cdk 2 and cdk 4 were inhibited after Energi-702 treatment. We also found that tumor suppressor gene p27 and p53 have significant elevation after Energi-702 treatment. On the other hand, the western blot result showed the activation of caspase-3, caspase-9, and PARP by Energi-702. In parallel, Energi-702 significantly decreased the level of anti-apoptotic protein, Bcl-2. Taken together, these findings indicate that Energi-702 diminished cell viability through cell cycle arrest and apoptosis. Shao-Hsuan Kao 高紹軒 2013 學位論文 ; thesis 66 zh-TW |
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碩士 === 中山醫學大學 === 生化暨生物科技研究所 === 101 === AMP-activated protein kinase (AMPK) is a key player in maintaining energy homeostasis in response to metabolic stress. Published studies indicate that AMPK activation strongly suppresses cell proliferation in
non-malignant cells as well as in tumour cells. This study examined the anti-tumor mechanism of Energi-702 (AMPK activator) on osteosarcoma cell lines (U2OS & 143B). Cell viability was detected by the MTT assay and cell morphology was observed after drug administration. After treated with Energi-702 for 24 hour, osteosarcoma cell lysates were collected. Western blot results demonstrate that cell cycle-associate proteins cyclin D1, cyclin E, cdk 2 and cdk 4 were inhibited after Energi-702 treatment. We also found that tumor suppressor gene p27 and p53 have significant elevation after Energi-702 treatment. On the other hand, the western blot result showed the activation of caspase-3, caspase-9, and PARP by Energi-702. In parallel, Energi-702 significantly decreased the level of anti-apoptotic protein, Bcl-2. Taken together, these findings indicate that Energi-702 diminished cell viability through cell cycle arrest and apoptosis.
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author2 |
Shao-Hsuan Kao |
author_facet |
Shao-Hsuan Kao Kim Chuan Chan 陳金釧 |
author |
Kim Chuan Chan 陳金釧 |
spellingShingle |
Kim Chuan Chan 陳金釧 Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
author_sort |
Kim Chuan Chan |
title |
Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
title_short |
Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
title_full |
Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
title_fullStr |
Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
title_full_unstemmed |
Investigating anti-tumor effects of Energi-702 on human osteosarcoma cells |
title_sort |
investigating anti-tumor effects of energi-702 on human osteosarcoma cells |
publishDate |
2013 |
url |
http://ndltd.ncl.edu.tw/handle/12191198435622856051 |
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