Title :
Growth Inhibition and Induction of Apoptosis in Sarcoma 180 Cells by Juglone in Vivo
Author :
Ji Yu bin ; Qu Zhong yuan ; Zou Xiang ; Cui Lan ; Hu Guo Jun
Author_Institution :
Eng. Res. Center of Natural Antineoplastic Drugs, Harbin Univ. of Commerce, Harbin
Abstract :
To study the effect of growth inhibition and induction of apoptosis in sarcoma 180 cells by juglone in vivo. S180 tumor-bearing mice were set up to investigate the effects of juglone on tumor growth inhibition and apoptosis. 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 in S180 cells. The experimental results showed that the tumor inhibition rate at the dosage of 2, 4 and 8mumol/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). 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. Juglone can inhibit the growth and induce apoptosis of sarcoma 180 cells in vivo.
Keywords :
bio-optics; biochemistry; cancer; cellular biophysics; drugs; molecular biophysics; optical microscopy; transmission electron microscopy; tumours; HE staining; S180 tumor-bearing mice; antitumor drugs; apoptotic bodies formation; chromatin condensation; chromatin margination; flow cytometry; in vivo juglone effects; nuclear envelope; optical microscope; pathomorphologic changes; sarcoma 180 cell apoptosis induction; subdiploid peak; transmission electron microscopy; tumor cell growth inhibition rate; tumor therapy; Abdomen; Animals; Drugs; Humans; In vivo; Mice; Neoplasms; Research and development; Transmission electron microscopy; Tumors;
Conference_Titel :
Future BioMedical Information Engineering, 2008. FBIE '08. International Seminar on
Conference_Location :
Wuhan, Hubei
Print_ISBN :
978-0-7695-3561-6
DOI :
10.1109/FBIE.2008.10