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dc.contributor.author林靜敏zh_TW
dc.contributor.author廖光文zh_TW
dc.contributor.authorLin, Ching-Minen_US
dc.contributor.authorLiao, Kuang-Wenen_US
dc.date.accessioned2018-01-24T07:42:58Z-
dc.date.available2018-01-24T07:42:58Z-
dc.date.issued2015en_US
dc.identifier.urihttp://etd.lib.nctu.edu.tw/cdrfb3/record/nctu/#GT079929802en_US
dc.identifier.urihttp://hdl.handle.net/11536/143105-
dc.description.abstract黃酮類化合物已有大量研究顯示其具有抗癌的潛力,根據結構的特性可再細分為不同的類別。7,7”-dimethoxyagastisflavone (DMGF)是雙黃酮化合物,屬於黃酮類化合物的其中一種,目前研究僅展現其具有抑制黃麴毒素產生及抗病毒的生物活性。根據本實驗室先前研究,我們發現DMGF在低濃度的劑量下即可造成A549肺癌細胞、HT29結腸直腸癌細胞和HepG2肝癌細胞死亡。然而,DMGF對於腫瘤發展時期,包含腫瘤增生,血管新生作用和腫瘤轉移的生物活性並未有太多討論。因此本研究主要目的為探討DMGF在腫瘤發展時期的生物活性,研究內容的第一部分目標是討論DMGF對於抑制腫瘤血管新生及腫瘤轉移的可行性和機制,第二部分目標則是討論DMGF抑制腫瘤增生的能力和機制。綜合以上研究成果顯示DMGF未來作為抗癌藥物的潛力。zh_TW
dc.description.abstractFlavonoids have shown an excellent antitumor activity. Based on their structures, they can be divided into several subgroups. 7,7”dimethoxyagastisflavone (DMGF), belongs to the biflavonoid group of flavonoids. In our laboratory, we found DMGF could induce cell death on A549 lung cancer cells, HT29 colon cancer cells and HepG2 hepatic cancer cell at lower dosage. However, the activities of DMGF on tumor progression, including proliferation, angiogenesis and metastasis is still not clear. Thus, the aim in this study is to investigate the bioactivities of DMGF for the suppression on tumor progression. Section one is to evaluate the effects and mechanisms of DMGF on tumor angiogenesis and metastasis, and section two is to demonstrate the ability of DMGF on tumor proliferation. Therefore, this study of DMGF can provide an insight on the potency as a chemotherapy drug.en_US
dc.language.isoen_USen_US
dc.subject黑色素瘤zh_TW
dc.subject腫瘤轉移zh_TW
dc.subject雙黃酮化合物zh_TW
dc.subject肌動蛋白絲聚合作用zh_TW
dc.subjectmelanomaen_US
dc.subjectmetastasisen_US
dc.subjectbiflavonoiden_US
dc.subjectF-actin polymerizationen_US
dc.title7,7”-dimethoxyagastisflavone 抑制黑色素瘤細胞 在腫瘤發展上的生物活性zh_TW
dc.titleThe bioactivities of 7,7”-dimethoxyagastisflavone for the suppression on tumor progression of melanoma cellsen_US
dc.typeThesisen_US
dc.contributor.department分子醫學與生物工程研究所zh_TW
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