Author/Authors :
Yılmaz, Seher Department of Anatomy - Yozgat Bozok University Faculty of Medicine - Yozgat, Turkey , Ülger, Harun Department of Anatomy - Erciyes University Faculty of Medicine - Kayseri, Turkey , Nisari, Mehtap Department of Anatomy - Erciyes University Faculty of Medicine - Kayseri, Turkey , Acer, Niyazi Department of Anatomy - Erciyes University Faculty of Medicine - Kayseri, Turkey , Ertekin, Tolga Department of Anatomy - Kocatepe University Faculty of Medicine - Afyon, Turkey , Hanım Yay, Arzu Department of Histology - Embriology - Erciyes University Faculty of Medicine - Kayseri, Turkey , Alpa, Şerife Department of Anatomy - Karatay University Faculty of Medicine - Konya,Turkey
Abstract :
In this study, the effects of different doses of curcumin application on Ehrlich ascites
tumor (EAT) created in the mice of BALB/c type were investigated.
Materials and Methods: Curcumin extracts can have hindering effect on tumor volume, vascular
density, EAT cells around the tissues, and can support apoptosis. EAT cells (1x106) received from
stock animals were injected intraperitoneally (IP) and subcutaneously (SC) to the animals. Then,
curcumin was administered IP. Doses of 25 mg/kg IP and 50 mg/kg were administered over 10 days
to the animals in the treatment groups in which ascites tumor was induced. The same doses were
administered over 15 days in the treatment groups in which solid tumor was induced.
Results: Histopathological examination in ascites tumor groups revealed that number of EAT cells at
surrounding tissues was smaller in the group received 50 mg/kg curcumin when compared to tumor
control group (P<0.05). The lowest increase in tumor volume was observed in the group received 25
mg/kg curcumin when compared to tumor control group (P<0.05).
Conclusion: It was demonstrated once again in our study that curcumin had an anti-tumoral effect on
both the development of ascites tumor created through EAT cells and the development of solid tumor.
Keywords :
Animal , Apoptosis , Cell , Curcumin , Factor VIII , Injection , Mice