• DocumentCode
    3120194
  • Title

    Curcumin Upregulate HO-1 Expression but Downregulate HO-2 Expression in SHSY5Y Cell

  • Author

    Shi, Xiaodong ; Li, Yu

  • Author_Institution
    Dept. of Pathology, Chongqing Med. Univ., Chongqing, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Curcumin, the most active constituent of turmeric, is currently one of the major anticance new drugs and has been reported to enhance Heme Oxygenase-1(HO-1) in human brain when oxidative stress occur. Keeping the balance of HO-1 and HO-2 plays an important role in the brain. However, few researches study the effects of curcumin on the two isoenzymes of HO. Here we investigated the effects of curcumin on the change of HO-1 and HO-2 in neuroblastoma cell line SHSY5Y. We found that the mRNA and protein levels of HO-1 were increased in a dose-and time-dependent manner (P<;0.05) in the cells after treated with Curcumin, whereas, the expression of HO-2 were gradually downregulated in a dose-and time-dependent manner (P<;0.05). A negative correlation was found between HO-1 and HO-2. These results indicate that Curcumin regulated HO-1 and HO-2 bilaterally, which may have an important effect on the pathogenesis and development of carcinoma, and may provide a new direction for disposing of carcinoma.
  • Keywords
    brain; cellular biophysics; drugs; enzymes; macromolecules; molecular biophysics; proteins; HO-1 expression; HO-2 expression; SHSY5Y cell; carcinoma; curcumin; heme oxygenase-1; human brain; isoenzymes; mRNA; neuroblastoma cell line; oxidative stress; protein levels; Biomembranes; Cancer; Degradation; Humans; Medical treatment; Neuroscience; Organisms; Pathology; Proteins; Stress;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5516396
  • Filename
    5516396