文化大學機構典藏 CCUR:Item 987654321/25950
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    Please use this identifier to cite or link to this item: https://irlib.pccu.edu.tw/handle/987654321/25950


    Title: 牛樟菇對已產生順鉑抗藥性之非小細胞肺腺癌細胞株的腫瘤毒殺及凋亡作用
    The Cytotoxic and Apoptotic Effects of Antrodia Cinnamomea on Cisplatin-resistant Human Non-small Cell Lung Cancer Cells
    Authors: 陳怡安
    Chen, Yi-An
    Contributors: 生物科技研究所
    Keywords: Lung cancer
    resistance
    cisplatin
    Chinese herb
    migration
    growth
    Date: 2013-06
    Issue Date: 2013-11-05 13:32:46 (UTC+8)
    Abstract: 肺癌是造成全世界最具威脅的癌症之一。 最主要的原因之一是在化學治療後會產生化療抗藥性。牛樟菇(Antrodia cinnamomea, AC)為一中草藥,又名樟芝或牛樟菇,為台灣特有真菌種。 目前已知AC具可能的抗癌作用,但其對肺癌仍無相關研究證實。 我們的實驗目的是探討AC是否可對化療抗藥性肺腺癌細胞株具有可能的毒殺效益。 我們先以臺灣肺腺癌患者的腫瘤檢体建立本土型肺腺癌細胞株,再以2 μg/ml和5 μg/ml不同濃度的化療藥物:順鉑(cisplatin) 建立出具有順鉑抗藥性的肺腺癌細胞株為細胞模式。 分別利用MTT assay、Wound healing assay、Flow cytometry 及Western blot來檢測AC是否會抑制細胞生長效果、細胞遷移能力、調控細胞週期及細胞凋亡及Bax/Bcl-2的蛋白表現量。結果顯示,AC對於肺腺癌細胞株有明顯的劑量依賴性毒殺作用。對具有順鉑抗藥性的肺腺癌細胞株而言,AC可以再提高其毒殺作用。Wound healing assay結果顯示,當AC濃度在20 mg/ml時,對於具有順鉑抗藥性的肺腺癌細胞株有顯著抑制其細胞遷移能力。AC可部分抑制S+G2M期,同時也會增加細胞凋亡比例。細胞凋亡蛋白分子Bax表現量增加和Bcl-2降低,推測AC可能會啟動內原性途徑的凋亡。 我們認為AC可能可以增強毒殺順鉑抗藥性肺腺癌細胞株能力。
    Lung cancer is one of the highest threaten cancers in the world. The most problem of the treatment is believed the chemodrug resistance. Antrodia cinnamomea (A. Cinnamomea; AC), a medicinal mushroom in Taiwan, has been shown anticancer activities. To investigate a novel anticancer effectiveness by pretreating patient-derived non-small cell lung cancer cells (NSCLCs) with cisplatin follwed by the administration of AC, the cisplatin-resistant patient derived NSCLCs were established with a 6-period of cisplatin treatments at 2 μg/ml and 5 μg/ml respectively. The capabilities of AC in cytotoxicity, migration, cell cycle, apoptosis and Bax/Bcl-2 proteins were evaluated respectively. Our results showed significant dose-dependent cytotoxicity in patients-derived NSCLCs. The nontoxic dose of AC enhanced the cytotoxicity of cisplatin-resistant patient-derived NSCLCs. The wound healing assay showed significant inhibitory effect in cisplatin-resistant NSCLCs when AC was treated at 20 mg/ml. Additionally, the enhanced apoptotic effect as characterized by increased Bax and decreased protein levels of Bcl-2 and S+G2M phase was reduced by AC treatment. Our results provide the first evidence that AC induced signigicant higher cytotoxicity and triggered intrinsic apoptosis in cisplatin-resistant NSCLCs.
    Appears in Collections:[Graduate Institute of Biotechnology ] thesis

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