透過您的圖書館登入
IP:3.138.141.202
  • 學位論文

具強入侵性A431癌細胞之篩選與定性,及其機制探討

In vitro selection and characterization of highly invasive tumor cells from A431 cell line

指導教授 : 李明亭

摘要


稍早的文獻顯示,並非所有的癌細胞都具有轉移的能力,真正具備轉 移能力的癌細胞可能只佔整個族群的0.1%,如何篩選出具有轉移能力的癌 細胞,成為近幾年重要的課題。癌細胞入侵血管是癌細胞轉移過程中最為 關鍵的步驟,本實驗室利用in vitro invasion assay,從A431 P 成功的 篩選出一批具有較強入侵能力的細胞,命名為A431 III,隨後進行細胞特 性之分析,並尋求可能的分子機制以解釋為何A431 III 比A431 P 更具侵 略性。 癌細胞要入侵,必須具備:1)降低細胞間附著力,2)增強細胞之 移動能力,3)增加matrix metalloproteinase (MMP)的釋放,分解 extracellular matrix (ECM),以利細胞之移動。初步的檢測顯示,A431 III 提高了MMP-9 之分泌量,並且具備較強的移動能力。此外,於cell spreading assay,我們發現A431 III 具有較強之細胞延展性,能過度活 化下游FAK,造成FAK 磷酸化上升。這些結果顯示A431 III 提升細胞之移 動能力與MMP 之分泌,可能經由FAK 調控,最終導致細胞具入侵性。

並列摘要


It was reported previously that not all of primary tumor possesses metastatic ability, and only about 0.1 percent tumor cells display higher invasive potential. How to isolate and identify these high invasive cells from primary tumor cells became an important issue in this field. Cell invasion is a fundamental component of tumor cell metastasis. In this study we use in vitro invasion assay appartus to select higher invasive carcinoma cells. The assay was performed by A431 P tumor cells on a porous membrane coated with matrix, after which the cell invading the matrix were collected (designated A431 I) and subcultured. The same assay was repeated until the A431 III was obtained. We then explore whether the A431 III has higher invasive potential. First, using gelatin zymography, we observed that A431 III secreted higher amounts of MMP-9 than that of A431 P. Secondly, using wound healing assay, cell attachment and spreading experiment. We observed that A431 III exhibit higher motility potential as well. This data suggest that A431 III possesses higher metastatic potential and FAK might play important role in regulate of cell motility and invasion.

並列關鍵字

MMP-9 FAK invasion

參考文獻


inhibitors: biological actions and therapeutic opportunities. J Cell Sci 115, 3719-27.
structure involved in purse string wound closure and cell polarity maintenance. J Cell
metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Nat Cell
adapter protein Cas: signal convergence and the determination of cellular responses.
Oncogene 20, 6448-58.

延伸閱讀