透過您的圖書館登入
IP:3.22.119.251
  • 學位論文

三環藥物Teroxirone對非小細胞肺癌細胞增生機制的探討

The Mechanistic Study of Growth Inhibition by Teroxirone in Human Non-Small Cell Lung Cancer Cells

指導教授 : 方剛
若您是本文的作者,可授權文章由華藝線上圖書館中協助推廣。

摘要


肺癌細胞依其組織型態可分為兩類:小細胞肺癌 (small cell lung cancer, SCLC) 以及非小細胞肺癌 (non-small cell lung cancer, NSCLC),而其中大多數屬於非小細胞肺癌。目前在臨床治療上經常使用的抗癌藥物 (例如: camptothecin, doxorubicin, etoposide, cisplatin) 容易產生抗藥性,導致治療的困難,因此本文開發目前臨床上還未徹底了解,但具有抗癌效果的化合物。 研究目標是發展小分子且低劑量的三環氧化物teroxirone,了解teroxirone如何引發細胞凋亡。實驗以MTT及細胞群落分析 (colony formation assay) 確認teroxirone確實能降低非小細胞肺癌的存活率。接著要確認非小細胞肺癌細胞的存活率下降的確是由於細胞凋亡所造成。再利用單細胞凝膠電泳 (single cell gel electrophoresis (SCGE) / comet assay),偵測teroxirone是否造成DNA 損傷。再利用propidium iodide (PI) 染色觀察teroxirone對細胞週期的影響,再利用二維流式細胞儀及DNA片段化實驗觀察teroxirone所誘導的細胞凋亡。 實驗結果顯示,teroxirone都會對NSCLC細胞造成不同程度DNA損傷,且細胞凋亡與p53的基因型有關。

關鍵字

Teroxirone DNA損傷 細胞凋亡

並列摘要


Lung cancer according to biological characteristics can be classified two types: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), most of which belong to non-small cell lung cancer. Clinical treatment used anticancer drugs (ex: camptothecin, doxorubicin, etoposide, cisplatin) frequently is easy to become resistant, leading to difficulties of treatment. The purpose of the thesis is to study the effectiveness of potential anticancer drugs. The goal of this study is to understand how low doses of teroxirone induce NSCLC cell apoptosis. Teroxirone can reduce the proliferation rate of non-small cell lung cancer on indicated by MTT assay and colony forming assay. To confirm the reduced NSCLC cell growth rate is indeed due to cell death. To be have used the single cell gel electrophoresis (SCGE) / comet assay to detect DNA damage. To be have used propidium iodide (PI) staining to observe that impact of teroxirone on cell cycle and the induced apoptosis by flow cytometry. Double staining with PI and Annexin V – FITC of cell death for apoptosis. At the same time, DNA fragmentation also confirmed teroxirone indeed induced cells apoptosis. The experimental results showed that teroxirone caused different degrees of DNA damage in NSCLC cells, but is caused apoptosis only occurred in p53 wild-type cells.

並列關鍵字

Teroxirone DNA damage apoptosis

參考文獻


Ames, M.M., Kovach, J.S. and Rubin, J. (1984) Pharmacological characterization of teroxirone, a triepoxide antitumor agent, in rats, rabbits, and humans, Cancer Research, 44, 4151-4156.
Ashkenazi, A. and Dixit, V.M. (1999) Apoptosis control by death and decoy receptors, Current Opinion in Cell Biology, 11, 255-260.
Atassi, G., et al. (1980) Antitumoral effect in mice of a new triepoxyde derivative: 1, 3, 5-triglycidyl-s-triazinetrione (NSC 296934), European Journal of Cancer, 16, 1561-1567.
Baldi, A., et al. (2011) Tumor suppressors and cell-cycle proteins in lung cancer, Pathology Research International, Article ID 605042.
Bonior, J., et al. (2012) Long-lasting effect of infant rats endotoxemia on heat shock protein 60 in the pancreatic acinar cells: involvement of toll-like receptor 4, International Journal of Inflammation, Article ID 354904.

延伸閱讀