Comparative Studies of Adriamycin and 28-Deacetyl Sendanin on In Vitro Growth Inhibition of Human Cancer Cell Lines

  • Kim, Hwan-Mook (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Oh, Goo-Taeg (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Han, Sang-Bae (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Hong, Dong-Ho (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Hwang, Bang-Yeon (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Kim, Young-Ho (Genetic Engineering Research Institute, KIST, Daeduk Science Town) ;
  • Lee, Jung-Joon (Genetic Engineering Research Institute, KIST, Daeduk Science Town)
  • Published : 1994.04.01

Abstract

The limonoid compound (28-deacetyl sendanin0 isolated from the fruit of Melia toosendan SIEB. et ZUCC. was evaluated on anticancer activity. According to a standard in vitro cytotoxicity assy, eight human cancer cell lines and SRB assay were introduced for present evaluation. As a positive standard, adriamycin was tested in parallel. The cell lines were originated from six different organs. In view of dose-response profiles to 28-deacetyl sendanin, the most sensitive cells were SF-539 and PC-3 which were derived from CNS and prostate, respecitively. In contrast, all the cell lines responded similarly to adriamycin to give rise to nearly indentical six cell lines were more sensitive to 28-deacetyl sendanin and two were more resistant. As a result, 28-deacetyl sendanin had more senstive and selective inhibitory effects on in vitro growth of human cancer cell lines in a comparison with adriamycin.

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