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http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/25745完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 郭彥彬 | |
| dc.contributor.author | Li-Chia Liu | en |
| dc.contributor.author | 劉力嘉 | zh_TW |
| dc.date.accessioned | 2021-06-08T06:27:50Z | - |
| dc.date.copyright | 2006-08-03 | |
| dc.date.issued | 2006 | |
| dc.date.submitted | 2006-07-26 | |
| dc.identifier.citation | Adams, J. M. and S. Cory (1998). 'The Bcl-2 protein family: arbiters of cell survival.' Science 281(5381): 1322-6.
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| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/25745 | - |
| dc.description.abstract | In Taiwan, Oral cancer is the fourth leading cause of cancer-related deaths in male population. Despite recent advances in radiotherapy and chemotherapy, the overall 5-year survival rate for patients with oral squamous cell carcinoma (OSCC) has not changed during the past two decades. More researches are needed to develop new therapertic and prevention methodologies to increase overall survival and improve patient’s living quality. Continuous investigation of new chemotherapeutic agents is thus needed. Epidemiological studies support the premise that dietary intake of Allium vegetables (e.g., garlic, onions and so forth) may lower the risk of varies types of cancer. Garlic-derived compounds have been shown to offer protection against oral tumor in animal models induced by carcinogens. Garlic-derived organosulfur compounds (OSCs) including diallyl sulfide (DAS), diallyl disulfide (DADS) and diallyl trisulfide (DATS) have the ability to suppress proliferation of human cancer cells by causing apoptosis. The different cell lines will be probably end up same or different mechanism of proliferation inhibition and apoptosis. However, the effects of OSCs on oral cancer proliferation is not clearly confirmed.
In our studies, the viability of oral cancer SAS and Ca9-22 cells were reduced upon a 24h exposure to DADS and DATS, however, DATS has better efficiency in inhibiting OSCC proliferation. The data indicated that SAS and Ca9-22 cells were reduced significantly on exposure to DATS in a concentration-dependent manner with each IC50 about 34 μM and 21 μM respectively. Per cell cycle distribution via flow cytometric analysis process, a 3h exposure of SAS cells to DATS (20μM) resulted increasing G2/M fraction. A 12h treatment of SAS cells with DATS resulted in a increase in the fraction of sub-G0/G1 cells. Western blot data showed that DATS treatment increased the protein level of p-Cdk1Tyr15 and Wee1, on the contrary, the protein level of Cdc25C and Cdk1 decreased. Our studies defined the mechanism of DATS-mediated G2 phase arrest, not mitotic arrest. In addition, the protein level alteration of PARP indicated that DATS-induced apoptosis in human oral cancer cells. Previous studies illustrated that DATS stimulated the intrinsic apoptotic pathway. In our study, DATS-induced apoptosis was decreased in the presence of caspase 8 or caspase 9 inhibitors (Z-LEHD-FMK, Z-IETD-FMK) in SAS and Ca9-22 cells, and the result was more effective when both of caspase 8 and capase 9 inhibitors treated. The data showed that DATS-induced apoptosis by activating intrinsic- and extrinsic-apoptosis pathway. Western blot data confirmed that DATS activates both apoptosis pathway in oral cancer cells with up-regulation of cytochrome c, DR5 and FADD. DATS-induced cell death was inhibited by N-acetyl cysteine in SAS and Ca9-22 cells, indicated that involvement of ROS was an important mechanism for DATS-induced apoptosis in human oral cancer cells. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-08T06:27:50Z (GMT). No. of bitstreams: 1 ntu-95-R93450007-1.pdf: 1999732 bytes, checksum: 34b03047d81b55ed75c2be985b6f23e4 (MD5) Previous issue date: 2006 | en |
| dc.description.tableofcontents | 中文摘要………………………………………………………..III
Abstract………………………………………………………….V 目錄……………………………………....................VII 第一章 緒論……………………………………………………..1 1-1、口腔癌......................................1 1-2、口腔癌之發生與腫瘤的發展過程................3 1-3、細胞凋亡....................................4 1-4、細胞凋亡之分子機制..........................6 1-5、Bcl-2基因家族...............................12 1-6、TNF receptors和death receptors..............15 1-7、細胞週期....................................20 1-8、蔥蒜屬植物之有機硫化合物....................22 第二章 實驗材料與方法................................29 2-1、細胞株培養..................................29 2-2、Sulforhodamine B分析法......................29 2-3、西方墨點法-細胞蛋白質的測定.................30 2-4、Caspase抑制作用.............................33 2-5、分析細胞質內的cytochrome c..................33 2-6、Cell death detection ELISA..................33 2-7、TdT-mediated dUTP-biotin nick end labeling (TUNEL)和(4’,6-diamidino-2-phenylindole) DAPI stain........34 2-8、統計分析……………………………..............35 第三章 實驗結果……………………………………..........36 3-1、DATS抑制SAS和Ca9-22細胞生長…………………...36 3-2、DATS對G2/M phase regulators之影響...........38 3-3、DATS誘導apoptosis反應.......................40 3-4、DATS對於apoptosis-related Bcl-2 family members之影響..........42 3-5、DATS誘導extrinsic apoptosis pathway的機制...44 3-6、DATS對ROS之影響.............................45 第四章 討論..........................................77 第五章 參考文獻......................................86 | |
| dc.language.iso | zh-TW | |
| dc.title | Diallyltrisulfide誘導人類口腔癌細胞凋亡機轉之研究 | zh_TW |
| dc.title | Diallyltrisulfide induced G2/M phase growth arrest and apoptosis in oral cancer cells | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 94-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 郭生興,蕭宏昇 | |
| dc.subject.keyword | DATS,細胞凋亡,細胞週期停滯,口腔癌細胞, | zh_TW |
| dc.subject.keyword | Diallyltrisulfide,apoptosis,G2/M phase arrest,oral cancer cells, | en |
| dc.relation.page | 96 | |
| dc.rights.note | 未授權 | |
| dc.date.accepted | 2006-07-27 | |
| dc.contributor.author-college | 醫學院 | zh_TW |
| dc.contributor.author-dept | 口腔生物科學研究所 | zh_TW |
| 顯示於系所單位： | 口腔生物科學研究所 | |
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