國家衛生研究院 NHRI:Item 3990099045/8792
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 12189/12972 (94%)
造訪人次 : 954611      線上人數 : 742
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    主頁登入上傳說明關於NHRI管理 到手機版
    請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/8792


    題名: Elevation of soluble guanylate cyclase suppresses proliferation and survival of human breast cancer cells
    作者: Wen, HC;Chuu, CP;Chen, CY;Shiah, SG;Kung, HJ;King, KL;Su, LC;Chang, SC;Chang, CH
    貢獻者: Institute of Cellular and Systems Medicine;National Institute of Cancer Research;Institute of Molecular and Genomic Medicine
    摘要: Nitric oxide (NO) is an essential signaling molecule in biological systems. Soluble guanylate cyclase (sGC), composing of alpha1 and beta1 subunit, is the receptor for NO. Using radioimmunoassay, we discovered that activation of sGC by treatment with bradykinin or sodium nitroprusside (SNP) is impaired in MCF-7 and MDA-MB-231 breast cancer cells as compared to normal breast epithelial 184A1 cells. The 184A1 cells expressed both sGC alpha1 and sGCbeta1 mRNAs. However, levels of sGCbeta1 mRNAs were relatively lower in MCF-7 cells while both mRNA of sGC subunits were absent in MDA-MB-231 cells. Treatment with DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine (5-aza-dC) increased mRNA levels of both sGCalpha1 and sGCbeta1 in MDA-MB-231 cells but only sGCbeta1 mRNAs in MCF-7 cells. The 5-aza-dC treatment increased the SNP-induced cGMP production in MCF-7 and MDA-MB-231, but not in 184A1 cells. Bisulfite sequencing revealed that the promoter of sGCalpha1 in MDA-MB-231 cells and promoter of sGCbeta1 in MCF-7 cells were methylated. Promoter hypermethylation of sGCalpha1 and sGCbeta1 was found in 1 out of 10 breast cancer patients. Over-expression of both sGC subunits in MDA-MB-231 cells induced apoptosis and growth inhibition in vitro as well as reduced tumor incidence and tumor growth rate of MDA-MB-231 xenografts in nude mice. Elevation of sGC reduced protein abundance of Bcl-2, Bcl-xL, Cdc2, Cdc25A, Cyclin B1, Cyclin D1, Cdk6, c-Myc, and Skp2 while increased protein expression of p53. Our study demonstrated that down-regulation of sGC, partially due to promoter methylation, provides growth and survival advantage in human breast cancer cells.
    日期: 2015-04-30
    關聯: PLoS ONE. 2015 Apr 30;10(4):Article number e0125518.
    Link to: http://dx.doi.org/10.1371/journal.pone.0125518
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1932-6203&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000353713100096
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84949528212
    顯示於類別:[張中和] 期刊論文
    [褚志斌] 期刊論文
    [夏興國] 期刊論文
    [龔行健] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    PUB25928539.pdf1588KbAdobe PDF683檢視/開啟


    在NHRI中所有的資料項目都受到原著作權保護.

    TAIR相關文章

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