• DocumentCode
    2498970
  • Title

    Antitumor Activity of Escin in Mice Cervical Carcinoma U_(14) In Vivo and Human Cervical Carcinoma Hela Cell Line In Vitro

  • Author

    Zhou, Xueying ; Wang, Changhai ; Fu, Fenghua

  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    Pollution made cancer a major disease threatening people´s health. In the search for new cancer drug treatments, natural products perform an essential role. Escin, a mixture of triterpene saponins extracted from Aesculus Wilsonii Rehd., was used to analyze the cell growth inhibitory effects and the induction of apoptosis in human cervical carcinoma Hela cancer cell line in vitro. The results of MTT cell viability assay showed that escin could induce significant concentration-dependent and time-dependent inhibition of cell growth, and the cell cycle was arrested at G1/S phase in the escin-treated cells. Apoptosis were detected and assessed by Acridine Orange/Ethidium Bromide Staining and Flow Cytometry. The antitumor efficacy of escin on mice cervical carcinoma U_(14) in vivo was investigated, at dose of 2.8 mg/kg escin had rather high inhibition ratio(43.5%) on U_(14) tumor growth.
  • Keywords
    cancer; cellular biophysics; drugs; gynaecology; patient treatment; tumours; Aesculus wilsonii Rehd; MTT cell viability assay; acridine orange staining; apoptosis detection; cancer drug treatment; cervical carcinoma; concentration-dependent cell growth inhibition; escin antitumor activity; escin-treated cell; ethidium bromide staining; flow cytometry; in vitro hela cell line; time-dependent cell growth inhibition; triterpene saponin; Biotechnology; Cervical cancer; Colon; Humans; In vitro; In vivo; Marine technology; Mice; Oceans; Pharmaceutical technology;
  • 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.2009.5162378
  • Filename
    5162378