Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/27196
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 17326/19632 (88%)
Visitors : 3561510      Online Users : 1105
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item:

    Title: a-Solanine抑制人類前列腺癌細胞侵入機制之探討
    The study of the mechanism of a-solanine on inhibiting invasion of human prostate cancer cells
    Authors: 林慧婷
    Contributors: 生物科技系
    Keywords: 人類前列腺癌
    matrix metalloproteinases
    Date: 2013
    Issue Date: 2014-03-10 20:40:49 (UTC+8)
    Abstract: a-Solanine為天然固醇類生物鹼,存在於發芽之馬鈴薯、番茄及許多茄科植物中。a-Solanine被發現具有抗癌之作用,如抑制腫瘤細胞增生及誘導細胞凋亡等。先前我們證明a-solanine藉由抑制基質金屬蛋白酶-2及-9 (MMP-2及-9) 之表達,進而抑制人類黑色素瘤細胞遷移和侵襲之能力。於本論文中,我們研究a-solanine抑制前列腺癌PC-3細胞體外轉移之機制。本研究利用不同濃度之a-solanine處理PC-3細胞後以MTT分析其對細胞存活之影響,接著選用不影響細胞生長之a-solanine劑量處理細胞,進行體外wound healing assay 和 Boyden chamber assay,以檢測a-solanine對細胞爬行和入侵能力之影響。此外利用即時定量聚合酶鏈鎖反應檢測PC-3細胞中miR-21、miR-138等microRNA和MMP-2/-9、組織金屬蛋白酶抑制蛋白TIMP-1/-2、細胞外基質金屬蛋白酶誘導因子 EMMPRIN和RECK等mRNA之表現。實驗數據顯示,隨著 a-solanine 濃度增加可有效抑制PC-3細胞之存活。當以12 uM之a-solanine處理後,細胞入侵能力有顯著性之抑制。另外,12uM的a-solanine可抑制MMP-2、MMP-9與EMMPRIN的mRNA表現,同時誘導了TIMP-2表現。另外,以a-solanine處理細胞後發現miR-21和miR-138都有受到調控。a-Solanine可誘導miR-138和抑制miR-21的表現。a-Solanine 亦可抑制vimentin,並同時誘導E-cadherin表現,顯示a-solanine可能可以藉由調控PC-3細胞進行上皮細胞轉型成間葉細胞(EMT)的過程來影響細胞的侵入作用。本研究發現a-Solanine可能經由影響miR-21與miR-138的表現,以及調控MMP-2/-9、EMMPRIN、TIMP-2表現,並抑制EMT而降低前列腺癌細胞PC-3的侵入作用。此結果為a-solanine的抗癌細胞轉移作用提供進一步的作用機轉。
    a-Solanine is a glycoalkaloid found in Solanaceae.a-Solanine possesses anti-carcinogenic properties, such as inhibiting proliferation and inducing apoptosis of tumor cells. Recently, we demonstrated that a-solanine suppressed migration and invasion of human melanoma cells. In the present study, we examined the inhibitory effect of a-solanine on metastasis of prostate cancer cell PC-3 in vitro. The effect of a-solanine on viability of prostate cancer cell PC-3 was determined by MTT assay. Then the effect of non-toxic doses of a-solanine on cell migration and invasion was examined by in vitro wound healing assay and Boyden chamber assay, respectively. Based on the previous studies, miR-21 suppressed MMP inhibitor RECK expression through the transcriptional repression. In addition, miR-138 may down regulate vimentin expression thereby affecting cell attachment and migration. There fore, the mRNA and micro RNA expression levels were detected by quantitative real-time polymerase chain reaction (qRT-PCR), including metalloproteinase-2 (MMP-2), MMP-9, tissue inhibitor of metalloproteinase-1/-2 (TIMP-1/-2), extracellular inducer of matrix metalloproteinase (EMMPRIN), micro RNA-21 (miR-21) and miR-138. Data indicated the a-solanine can inhibit the viability of human prostate cancer PC-3 cell in a dose-dependent manner. When treated with non-toxic doses of a-solanine, cell invasion was inhibited significantly. a-Solanine inhibits expression of MMP-2, MMP-9 and EMMPRIN, while induces expression of tissue inhibitor of metalloproteinase-1/-2 (TIMP-1/-2). a-Solanine also inhibits miR-21 and induces miR-138 expression in PC-3 cells. In addition, a-solanine reduces vimentin and elevates E-cadherin expression, suggesting a-solanine may inhibit epithelial-mesenchymal transition of PC-3 cells. Taken together, the results suggest that a-solanine inhibits invasion of PC-3 cells may be through suppressing expression of MMP-2, MMP-9, EMMPRIN and inducing expression of TIMP-2 and E-cadherin. These findings reveal new therapeutic potential for a-solanine in anti-metastatic therapy.
    Relation: 電子全文公開日期:20181201,學年度:101,52頁
    Appears in Collections:[Dept. of Biotechnology (including master's program)] Dissertations and Theses

    Files in This Item:

    File Description SizeFormat

    All items in CNU IR are protected by copyright, with all rights reserved.

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback