Potential genotoxicity and anti-tumor activity in tumor-bearing mice treated with zinc oxide nanoparticles and N-acetyl cysteine /
السميه الجنينيه المحتملة ووالنشاط المضاد للتورم فى الفئران الحاملة للورم والمعاملة بجسيمات أكسيد الزنك النانونية ون -أسيتيل سيستين
Shaymaa Mohamed Eissa Eldoh ; Supervised Mohamed Akmal Elghor , Salwa Farouk Sabet , Haidan Mostafa salem
- Cairo : Shaymaa Mohamed Eissa Eldoh , 2019
- 126 P. : charts , facsimiles ; 25cm
Thesis (Ph.D.) - Cairo University - Faculty of Science - Department of Zoology
Background: Several in vitro studies have revealed that zinc oxide nanoparticles (ZnONPs) were able to target cancerous cells selectively with minimal damage to healthy cells. In the current study, we aimed to evaluate the antitumor activity of ZnO-NPs in Ehrlich solid carcinoma (ESC) bearing mice by measuring their effect on the expression levels of P53, Bax and Bcl2 genes as indicators of apoptotic induction in tumor tissues. Also, we assessed the potential ameliorative or potentiation effect of 100 mg/kg of N-acetyl cysteine (NAC) in combination with ZnO-NPs. Materials and methods: ESC bearing mice were gavaged with three different doses of ZnO-NPs (50, 300 and 500 mg/kg body weight) alone or in combination with NAC for seven consecutive days. In addition to measuring the tumor size, pathological changes, zinc content, oxidative stress biomarkers and DNA damage in ESC, normal muscle, liver and kidney tissues were assessed. Results: Data revealed a significant reduction in tumor size with a significant increase in p53 and Bax and decrease in Bcl2 expression levels in the tissues of ZnO-NPs treated ESC bearing mice. Moreover, a significant elevation of MDA accompanied with a significant reduction of CAT and GST