• DocumentCode
    2520927
  • Title

    Studies on Inhibition of Juglone on Sarcoma 180 in Mice

  • Author

    Yubin Ji ; Qu, Zhong Yuan ; Zou, Xiang ; Cui, Lan ; Guo-Jun Hu

  • Author_Institution
    Eng. Res. Center of natural antineoplastic drugs, Harbin Univ. of Commerce Harbin, Harbin, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    To study the anti-tumor effect and mechanism of juglone on the mice xenotransplant model of sarcoma 180 in vivo. S180 tumor-bearing mice were set up to investigate the effects of juglone on tumor growth. After HE staining, the pathomorphologic changes of tumor cells were observed by optical microscope. The ultrastructural changes of tumor cells were observed by transmission electron microscopy. Flow cytometry was used to observe the apoptosis rate and cell cycle arrest in S180 cells. The experimental results showed that the tumor inhibition rate at the dosage of 2, 4 and 8 mumol/kg of juglone was 29.04%, 37.33%, 52.66% respectively. The tumor weight of all dose groups of juglone were lower significantly than that in blank control group (P<0.01). Under the optical microscope, the necrosis degree of the tumor cells increased significantly as the concentration of juglone increased compared with the blank control group. The typical morphological changes of apoptosis were observed, such as chromatin condensation, margination against nuclear envelope and formation of apoptotic bodies by transmission electron microscopy. The subdiploid peak was found and the apoptosis rate of juglone at the dosage of 2, 4 and 8 mumol/kg was 5.58plusmn0.63%, 6.66plusmn0.85%, 10.27plusmn1.05% respectively. The percentage of cells in G1 phase of the cell cycle was decreased, whereas the amount of cells in the G2/M phase was increased. Juglone perhaps induced G2/M cell cycle arrest, which needs further research. Inducing apoptosis and G2/M phase cycle arrest play important roles in the anti-tumor effect of juglone.
  • Keywords
    cancer; cellular biophysics; optical microscopy; organic compounds; transmission electron microscopy; tumours; HE staining; antitumor effect; chromatin condensation; flow cytometry; juglone inhibition; margination; mice xenotransplant model; optical microscopy; sarcoma; transmission electron microscopy; Abdomen; Animals; Business; Mice; Neoplasms; Optical microscopy; Pharmaceuticals; Research and development; Transmission electron microscopy; Tumors;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5163442
  • Filename
    5163442